Exhibit 99.2

Merus Labs International Inc.

First Quarter Report Fiscal 2017

For the Three Months Ended December 31, 2016 and 2015

MERUS LABS INTERNATIONAL INC.

MANAGEMENT’S DISCUSSION AND ANALYSIS

For the three months ended December 31, 2016 and 2015

This Management’s Discussion and Analysis (the “MD&A”) sets out the financial performance, results of operations and condition of Merus Labs International Inc. (the “Company” or “Merus”) for the three months ended December 31, 2016 (“Q1 2017”) compared to the three months ended December 31, 2015 (“Q1 2016”). The analysis should be read in conjunction with the accompanying unaudited interim consolidated financial statements (the “Financial Statements”) for the three months ended December 31, 2016 and 2015 and the related notes thereto. References to “FY 2016” and to “FY 2017” are to our fiscal years ended September 30, 2016 and 2017 respectively.

The date of this MD&A is February 13, 2017.

FORWARD-LOOKING STATEMENTS

This MD&A contains certain statements or disclosures that may constitute forward-looking information or statements (collectively, “forward-looking information”) under applicable securities laws. All statements and disclosures, other than those of historical fact, which address activities, events, outcomes, results or developments that management of the Company anticipates or expects may or will occur in the future (in whole or in part) should be considered forward-looking information. In some cases, forward-looking information can be identified by terms such as “forecast”, “future”, “may”, “will”, “expect”, “anticipate”, “believe”, “could”, “potential”, “enable”, “plan, “continue”, “contemplate”, “pro forma” or other comparable terminology. Forward-looking information presented in such statements or disclosures may, amongst other things include:

• our expectations regarding sales from its existing products, including its sales forecasts;

• our ability to acquire new products;

• our expectations regarding our ability to raise capital, including our ability to secure the financing necessary to acquire new products;

• our expectations regarding sales from products that we acquire or license;

• our forecasts regarding our operating expenditures, including general and administrative expenses,

• our expectations regarding the development of our target markets;

• our expectations regarding government regulations of our products and any new products that we acquire;

• our expectations regarding currency exchange rates;

• our expectations regarding income taxes;

• our plans, objectives and targets for future revenue growth and operating performance;

• our plans and objectives regarding new products that we may acquire; and

• our forecasted business results and anticipated financial performance.

The forward-looking information in statements or disclosures in this MD&A is based (in whole or in part) upon factors which may cause actual results, performance or achievements to differ materially from those contemplated (whether expressly or by implication) in the forward-looking information. Those factors are based on information currently available, including information obtained by Merus from third-party industry analysts and other third-party sources. Actual results or outcomes may differ materially from those predicted by such statements or disclosures. While we do not know what impact any of those differences may have, our business, results of operations, financial condition and credit stability may be materially adversely affected. Factors that could cause actual results or outcomes to differ materially from the results expressed or implied by forward-looking information include, among other things:

• our ability to successfully market and sell our products;

• our ability to service existing debt;

• our ability to increase sales of our existing products;

• our ability to acquire new products and, upon acquisition, to successfully market and sell new products that we acquire;

• our ability to achieve the financing necessary to complete the acquisitions to new products;

• market conditions in the capital markets and the biopharmaceutical industry that make raising capital or consummating acquisitions difficult, expensive or both;

• unanticipated cash requirements to support current operations, to expand our business or for capital expenditures;

• the acceptance of our products by regulatory and reimbursement agencies in various territories including Canada and Europe and inclusion on drug benefit formularies, hospital formularies and acceptance by pharmacies, physicians and patients in the marketplace;

• determinations by regulatory and reimbursement agencies in various countries including Canada and Europe regarding the maximum reimbursement price payable for the products that we sell;

• core patent protection for our product portfolio has expired or will expire in the future, which could result in significant competition from generic products resulting in a significant reduction in sales;

• delays or setbacks with respect to governmental approvals, or manufacturing or commercial activities;

• the patient health, legal, and commercial risks associated with patient adverse events or side effects resulting from the use of our products;

• the inability to adequately protect our key intellectual property rights;

• the loss of key management or scientific personnel;

• the activities of our competitors and specifically the commercialization of innovative or generic products that compete in the same category as our products;

• the risk that we are not able to arrange sufficient, cost-effective financing to repay maturing debt and to fund expenditures, future operational activities and acquisitions, and other obligations; and

• the risks associated with legislative and regulatory developments that may affect costs, revenues, the speed and degree of competition entering the market, global capital markets activity and general economic conditions in geographic areas where we operate.

Investors should review the full discussions as to material risks and uncertainties, and factors and assumptions used to develop forward-looking statements, included in our Annual Information Form for the year ended September 30, 2016 (our “2016 AIF”), our management’s discussion and analysis of results of operations for the year ended September 30, 2016 (our “2016 MD&A”) and our related annual report on Form 40-F.

Various assumptions or factors are typically applied in drawing conclusions or making the forecasts or projections set out in forward-looking information. Those assumptions and factors are based on information currently available, including information obtained from third-party industry analysts and other third-party sources. In some instances, material assumptions and factors are presented or discussed elsewhere in this MD&A in connection with the statements or disclosure containing the forward-looking information. You are cautioned that the following list of material factors and assumptions is not exhaustive. The factors and assumptions include, but are not limited to:

• no unforeseen changes in the legislative and operating framework affecting our business;

• no unforeseen changes in the prices for our products in markets where prices are regulated;

• no unforeseen changes in the regulatory environment for our products;

• no unforeseen changes in our ability to maintain a consistent supply of regulatory quality approved products;

• a stable competitive environment; and

• no significant event occurring outside the ordinary course of business such as a natural disaster or other calamity.

Merus is not obligated to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by applicable laws. Because of the risks, uncertainties and assumptions contained herein, security holders should not place undue reliance on forward-looking statements or disclosures. The foregoing statements expressly qualify any forward-looking information contained herein.

The above list of risk factors is not exhaustive. Other factors which could cause our actual results, performance or achievements to differ materially from those contemplated (whether expressly or by implication) in the forward-looking statements or other forward-looking information are disclosed in our publicly filed disclosure documents.

All historical financial information is prepared in accordance with IFRS, unless otherwise noted, and is expressed in Canadian dollars.

Corporate OVERVIEW

We are a specialty pharmaceutical company focused on acquiring and optimizing legacy and growth products. We leverage our expertise and scalable commercial platform in Europe, Canada and select other markets to deliver value. We currently own, market and distribute the following pharmaceutical products within the territories described below pursuant to license and other intellectual property rights that we have acquired:

Name of Product	Acquired From	Indication	Territory Rights	Patent Protection
Nitrates Portfolio: Elantan®, Isoket® and Deponit®	UCB Pharma (February 2016)	Acute and chronic coronary artery disease	Twenty European countries, Mexico, Turkey and South Korea	None
Sintrom®	Novartis Pharma AG (September 2014)	Treatment and prevention of thromboembolic diseases	Certain European countries including Spain, Italy, Greece, Romania and Bulgaria	None
Emselex®/Enablex®	Novartis Pharma AG (July 2012)	Treatment of overactive bladder syndrome	Canada and Europe (excluding France, Spain and Italy)	Core patents expired in 2016, Supplemental Protection Certificate provides barrier through October 2019
Surgestone® and Provames®	Sanofi (March 2016)	Variety of women’s health indications	France	None
Speciafoldine®	Sanofi (March 2016)	Macrocytic anemia	France	None

Tredemine®	Sanofi (March 2016)	Tapeworm	France	None
Salagen ®	Novartis Pharma AG (May 2015)	Treatment of symptoms of dry eye and dry mouth disorders; indicated for xerostomia following radiation therapy	Territory comprised of 50 countries, the majority of which are European counties, inclusive of France, Germany, Italy, Spain and the United Kingdom, and which also include Russia and a number of Western Asian countries	None
Estraderm MX®	Novartis Pharma AG (May 2015)	Treatment of signs and symptoms of estrogen deficiency due to menopause; prevention of accelerated postmenopausal bone loss	United Kingdom, Australia, Italy, Colombia, Spain, Poland and Singapore, and other EU countries (subject to Novartis supply obligation limitations)	None
Vancocin®	Iroko (May 2011)	Treatment of gastrointestinal tract bacterial infections (including C. difficile)	Canada	None

Our products are described in detail in our 2016 AIF.

Merus’ head office is located at Suite 2110, 100 Wellington St. West, P.O. Box 151, Toronto, Ontario M5K 1H1. Our telephone number is 905-726-0995.

Our common shares are publicly traded on the Toronto Stock Exchange (the “TSX”) under the symbol “MSL” and on NASDAQ under the symbol “MSLI”.

CORPORATE STRATEGY

The primary focus of our corporate strategy is to acquire and optimize prescription medicines in the following categories:

• On-patent but at maturity stage of product life cycle

• Branded generics

• Under-promoted products

• Niche market pharmaceuticals

• Growth products with a concentrated prescriber base that have been recently approved, or are expected to be approved within two years of acquisition

• Products with annual sales below the critical threshold for large pharma

We have determined to expand our corporate strategy in order to target new medicines with growth potential. We believe that pursuing this expanded corporate strategy has the potential to complement the strong foundation that we have built through our existing legacy product portfolio and provide additional growth opportunities for our business. We have not completed any acquisitions of growth medicines to date, but our business development team is currently evaluating growth medicine products as part of their mandate. As with potential legacy product acquisitions, acquisitions of growth medicine products will be contingent on our being able to negotiate acceptable acquisition terms and securing any necessary financing to fund and integrate the acquisition.

Our corporate growth strategy is driven by a product acquisition plan that employs an opportunistic approach to sourcing product acquisition candidates. This approach allows us to source pharmaceutical products across broad therapeutic classes and provides us access to acquisition targets not available to other players. Although we have a broad therapeutic focus, opportunities are pursued if a dedicated small-scale sales force can deliver incremental product sales. Our geographic focus is primarily Europe and Canada.

The result of this corporate strategy is a diversified product portfolio. To manage such a product portfolio, we layer a low-cost operating model on top of our light corporate infrastructure. We leverage the expertise of third-party contract manufacturing and regulatory service providers and maintain complete flexibility.

OVERVIEW

Material developments in our business in the preceding twelve months up to the date of this MD&A are summarized as follows:

Date	Event
July 4, 2016	Merus announces completion of first regularly scheduled quarterly payment of principal under its new credit facility
July 1, 2016	Merus appoints Michael Bumby as Chief Financial Officer; and Frank Fokkinga as Vice-President, Global Regulatory Affairs, Quality and Compliance
March 7, 2016	Merus completes acquisition of women’s health portfolio from Sanofi S.A. (“Sanofi”)
March 1, 2016	Merus completes $27 million bought deal private placement of subscription receipts
February 4, 2016	Merus completes acquisition of nitrates portfolio from UCB Pharma GmbH (“UCB”)
February 1, 2016	Merus enters into $180 million amended and restated credit agreement with Bank of Montreal, CIBC and a syndicate of lenders (our “Amended and Restated Credit Agreement”)

Details of the material developments described above have been provided in our 2016 AIF and our 2016 MD&A.

OVERALL PERFORMANCE

Revenues increased to $26.1 million for Q1 2017 from $15.9 million for Q1 2016, representing a year-over-year increase of 64%. Gross Basis Revenues¹ increased to $30.9 million during Q1 2017 from $18.3 million for Q1 2016, representing a year-over-year increase of 69%. The increases in revenues and Gross Basis Revenues primarily reflect our expanded portfolio of pharmaceutical products in Q1 2017 in comparison to Q1 2016 resulting from the acquisition of the nitrates portfolio from UCB and the women’s health portfolio from Sanofi in the second quarter of 2016 (“Q2 2016”).

¹ See below under “Non-IFRS Financial Measures” for a discussion of Gross Basis Revenues and a reference to the reconciliation to the results presented in the financial statements.

Net loss increased to $6.3 million for Q1 2017 from $0.9 million for Q1 2016. The increase in net loss is primarily attributable to foreign exchange losses of $3.7 million in Q1 2017, compared to foreign exchange gains of $0.6 million in Q1 2016, resulting in a $4.3 million negative impact on operating income. Increased finance costs of $2.2 million in Q1 2017, compared to $0.9 million in Q1 2016, also contributed $1.3 million to the increase in our net loss. Increases in amortization expenses, general and administrative expenses and selling and marketing expenses in Q1 2017 over Q1 2016 resulting from our expanded product portfolio and our related expanded operations also impacted our net loss, however these increases were overall matched by the increase in our gross margin in Q1 2017 over Q1 2016.

EBITDA² decreased to $5.3 million for Q1 2017 from $7.5 million for Q1 2016, representing a year-over-year decrease of 29%. The decrease in EBITDA was largely attributable to the foreign exchange loss in Q1 2017, compared to the foreign exchange gain in Q1 2016. Adjusted EBITDA² increased to $10.8 million during Q1 2017 from $8.5 million for Q1 2016, representing a year-over-year increase of 27%.

² See below under “Non-IFRS Financial Measures” for a reconciliation of EBITDA and Adjusted EBITDA to net loss.

Assets decreased to $361 million as at December 31, 2016 from $375 million as at September 30, 2016 as a result of product amortization and foreign exchange differences on the revaluation of foreign subsidiaries and monetary assets. Total liabilities decreased to $173 million as at December 31, 2016 from $178 million as at September 30, 2016 as we made a further installment payment of principal under our long term debt. We had a working capital deficit of $10.2 million as at December 31, 2016, compared to a working capital deficit of $13.7 million as at September 30, 2016. The decrease in working capital deficit is primarily attributable to a decrease in long term debt due within one year to $30.5 million as at December 31, 2016 from $36.1 million as at September 30, 2016. Our working capital deficit as at December 31, 2016 is primarily attributable to the current portion of our long-term debt in the amount of $30.5 million which is repayable under the Amended and Restated Credit Agreement, as further discussed below. As at December 31, 2016, excluding provisions and obligations related to the current portion of our long-term debt, we had working capital of $20.3 million compared to $22.5 million at September 30, 2016.

Cash provided by operating activities was $4.9 million for Q1 2017, compared to $6.9 million for Q1 2016. We plan to use cash provided by operating activities to fund the current portion of our long-term debt and build working capital for our expanded operations.

Overall, Q1 2017 reflected the third consecutive quarter with our current expanded product portfolio and reflected our ongoing efforts to integrate our new products into our business operations.  During Q1 2017, we continued refining our pan-European platform, upgrading our enterprise resource planning and business intelligence systems, and streamlining all of our related processes. In addition, we focused on cost-savings measures with results anticipated to be realized in the second half of 2017.

NON-IFRS FINANCIAL MEASURES

We use the following non-IFRS measures in this MD&A:

• Gross Basis Revenue,

• EBITDA, and

• Adjusted EBITDA.

These non-IFRS measures are not recognized measures under IFRS and do not have a standardized meaning prescribed by IFRS. These measures are defined with reference to the nearest comparable IFRS measure in order that a reconciliation to the nearest comparable IFRS measure can be completed. Accordingly, these measures may not be comparable to similar measures presented by other companies. We use these non-IFRS measures in order to provide additional financial information to complement the closest IFRS measures in order to provide investors with a further understanding of our operations from management’s perspective. Investors should not consider that these non-IFRS measures are a substitute for analyses of the financial information that we report under IFRS. We use these non-IFRS measures in order to provide investors with a supplemental measure of our operating performance and thus highlight trends in our business that may not otherwise be apparent when relying solely on IFRS measures.

The definition of each of these non-IFRS financial measures is presented below:

Gross Basis Revenue

As is necessary and customary in the pharmaceutical industry due to the regulatory framework, once we complete the acquisition of a pharmaceutical product, we enter into a transition phase during which the marketing authorizations necessary for us to legally market and sell the product are transferred to us from the vendor, for each country comprising the territory for which rights are acquired. Pending the completion of the transfer of the marketing authorizations, the vendor, in our case typically a major pharmaceutical company, will continue to market and sell the product in the acquired territories on our behalf. As they remain the legal seller of the products, the vendor remits to us a “profit transfer” amount that is calculated from the product sales, less the associated cost of goods, and less certain other expenses including an agreed amount payable to the vendor as consideration for their administering the product sales during the transition period. This arrangement is typically set out in a transition services agreement which is negotiated as part of the product acquisition agreement and is executed at the time of the closing of the product acquisition. The term of the transition services agreement is typically in the range of 9 to 12 months, and we are typically obligated to pursue transfer of the marketing authorizations in order that the transition services agreement is in effect for the shortest period possible.

For products that are in the transition phase during a reporting period, we have presented revenue on a net basis, as required in accordance with the Company’s accounting policies and IFRS, and on a “Gross Basis Revenue” basis. Reporting revenue on a net basis, as presented in our financial statements, requires that we report only the “profit transfer” amount that we receive from the vendor, and does not reflect the underlying sales value of the product to customers. Reporting on a “Gross Basis Revenue” basis better reflects both the actual sales of the product and the corresponding cost of goods sold associated with the product in the appropriate financial statement line items. This information is provided in order to allow investors to understand the actual underlying revenue for the recently acquired products in order that they can be comparable to other products and future periods.

Gross Basis Revenue is a non-IFRS measure that we define as the revenue that we would have received had we held title to and sold our products directly to our customers during the transition period. Gross Basis Revenue is calculated from revenue, which are reflected in our financial statements, by adding back the cost of goods sold and selling expenses that are associated with the revenue as reported by the vendor. We have provided a reconciliation of Gross Basis Revenues to net revenue on a product-by-product basis in this MD&A under Results of Operations.

EBITDA

We define EBITDA as earnings before interest expense, taxes, depreciation and amortization. We believe EBITDA to be an important measurement that allows us to assess the operating performance of our ongoing business on a consistent basis without the impact of amortization, debt service obligations and other non-operating items. We exclude amortization because its level depends substantially on non-operating factors such as the historical cost of intangible assets.

Adjusted EBITDA

We define Adjusted EBITDA as earnings before interest expense, taxes, depreciation, amortization, impairment charges, non-cash stock based compensation, foreign exchange and derivative gains or losses, investment income or expense, one-time legal settlement costs, and acquisition costs. We believe Adjusted EBITDA to be an important measurement that allows us to assess the operating performance of our ongoing business on a consistent basis without the impact of amortization and impairment expenses, debt service obligations, other non-operating and non-cash items, and one-time events. We exclude amortization and impairment expenses because their level depends substantially on non-operating factors such as the historical cost of intangible assets.

The following table provides a reconciliation of EBITDA and Adjusted EBITDA to net loss for the period, being the most directly comparable IFRS measure:

	Three Months ended December 31
	2016	2015
Net loss for the period	$  (6,317,410)	$  (915,020)
Interest expense	2,208,562	947,629
Income tax expense	475,009	131,561
Depreciation	13,166	3,854
Amortization	9,134,300	7,356,701
EBITDA	$  5,320,919	$  7,524,725
Add/(Deduct):
Acquisition costs	-	352,319
Legal settlement costs (excluding professional fees)	998,176	-
Non-cash stock based compensation	859,702	1,092,173
Investment (income) expense	-	(117)
Foreign exchange losses (gains)	3,748,357	(570,697)
Derivative losses (gains)	(77,410)	136,872
Adjusted EBITDA	$  10,849,744	$  8,535,275

RECENT DEVELOPMENTS

Arbitration Proceeding

In August 2014, we received notice of a request for arbitration from LG Life Sciences (“LGLS”), the original owner of the Company’s former Factive® product.  This request for arbitration was based on the original license agreement entered into by LGLS and Chiesi.  The arbitration proceedings were brought under the rules of arbitration of the International Chamber of Commerce (the “ICC Arbitration”) named us as a respondent together with Chiesi and Vansen Pharma, Inc.  The request for arbitration included the allegation that Chiesi did not have the legal right to transfer the Factive product to Merus under the Factive Asset Purchase Agreement. LGLS sought an award for damages relating to an alleged breach of contract, as well as disgorgement of revenue and other benefits derived by us from sales of Factive. The ICC arbitration tribunal dismissed the claims of LGLS against us in the decision of the panel issued in May 2016.  Additionally, the ICC arbitration panel also dismissed the claims that we and Chiesi had each asserted against one another, seeking indemnity and damages related to LGLS’s claim.  The ICC arbitration tribunal issued a final decision in Q4 2016 denying any liability of Merus to LGLS resulting from Vansen’s failure to return the license to sell Factive to LGLS. Accordingly, we have been successful in defending these claims under the ICC Arbitration.

We were party to an arbitration proceeding under the International Centre for Dispute Resolution of the American Arbitration Association (the “AAA Arbitration”) brought by Chiesi under the Factive Asset Purchase Agreement. Chiesi claimed indemnification from us with respect to: (i) cost incurred by Chiesi to reimburse wholesalers for expired or returned Factive product, (ii) investigative costs incurred by Chiesi to defend claims from wholesalers, (iii) the cost of any government rebates paid by Chiesi in connection with sales of Factive after execution of the Asset Purchase Agreement, and (iv) legal costs incurred by Chiesi to defend against LGLS’s original claim under the ICC Arbitration. 

We entered into a settlement agreement in late Q1 2017 in respect of these claims pursuant to which the AAA Arbitration proceedings have been dismissed. We paid the amount required under the settlement agreement, which represented partial payment of the amounts claimed against us, in January 2017. An amount of $1.0 million was expensed in general and administrative expense in Q1 2017, which was comprised of the legal settlement amount of US$0.65 million and $0.13 million in unrecoverable deposits paid towards the original arbitration proceedings.

RESULTS OF OPERATIONS FOR THE THREE MONTHS ENDED DECEMBER 31, 2016 AND 2015

The Company’s results of operations and financial position for the three months ended December 31, 2016 and 2015 are presented below:

Balance Sheet	As at
	December 31, 2016	September 30, 2016
Current Assets:	51,599,076	44,816,341
Total Assets:	360,842,006	375,384,718
Current Liabilities:	61,835,538	58,547,742
Non-Current Liabilities:	111,100,163	119,070,535
Total Liabilities	172,935,701	177,618,277
Income Statement	Three Months ended December 31
	2016	2015
Revenue:
Enablex/Emselex	$   5,603,912	$   7,794,298
Sintrom	5,620,396	5,258,262
Nitrates Portfolio	7,931,656	-
Sanofi Portfolio	3,095,895	-
Salagen	2,035,699	1,611,363
Vancocin	606,196	836,796
Estraderm	1,175,050	425,132
Total Revenue	26,068,804	15,925,851
Cost of Goods Sold	8,119,768	4,621,987
Gross Margin	$   17,949,036	$   11,303,864
Operating Expenses	$  21,660,285	$  11,002,939
Operating Income (Loss)	(3,711,249)	300,925
Other Expense (Income)	2,606,161	1,215,945
Net Loss	$  (6,317,410)	$  (915,020)
Loss per share (basic  and diluted)	$0.05	$0.01
Dividends Declared	Nil	Nil

Revenue

Revenue for Q1 2017 increased to $26.1 million from $15.9 million for Q1 2016, representing a year-over-year increase of 64%. This increase in revenue is primarily attributable to the increase in the number of products in our portfolio resulting from the acquisitions of the UCB and Sanofi product portfolios in Q2 2016, combined with the continued transition of our acquired products from a net revenue accounting basis to a gross revenue accounting basis as the associated marketing authorizations are transferred to us.

Gross Basis Revenue for Q1 2017 increased to $30.9 million from $18.3 million for Q1 2016, representing a year-over-year increase of 69%. This increase in revenue is primarily attributable to the increase in the number of products in our product portfolio resulting from our FY 2016 acquisitions. The reconciliation of Gross Basis Revenue to Revenue, being the nearest IFRS measure, is provided below under “Product Portfolio Revenue”. See also above under “Non-IFRS Measures”.

Revenue in Q1 2017 includes sales of the nitrates portfolio acquired from UCB and the women’s health portfolio acquired from Sanofi in Q2 2016. Revenue in Q1 2016 did not include revenues from these products.

Sales in the United Kingdom remain in the range of 10% of our total product sales. Accordingly, we anticipate that our business will not be materially impacted by Brexit.

Cost of Sales

Cost of goods sold for Q1 2017 increased to $8.1 million from $4.6 million in Q1 2016, representing a year-over-year increase of 76%. As with the increase in revenue, the increase in costs of goods sold was primarily attributable to the growth of our product portfolio from Q1 2016 to Q1 2017 combined with the transition of recently acquired products from net revenue accounting to gross revenue accounting. Certain amounts in the prior period have been reclassified from selling and marketing expense to cost of goods sold in order to better reflect true cost of goods sold and improve comparability.

On a gross basis, cost of goods sold for Q1 2017 increased to $13.0 million from $7.0 million in Q1 2016. This increase in cost of goods sold was primarily attributable to the growth of our product portfolio from Q1 2016 to Q1 2017.

Gross Margin

Gross margin for Q1 2017 was $17.9 million compared to $11.3 million for Q1 2016, representing a year-over-year increase of 59%. Gross margin as a percentage of revenue for Q1 2017 was 69%, compared to 71% in Q1 2016. The small decrease in our gross margin as a percentage of revenue was a result of product and geographic mix and the addition of the nitrates portfolio. Details of the transition from net revenue to Gross Basis Revenue on a product-by-product basis are described further below under “Product Portfolio Details”.

Gross margin as a percentage of Gross Basis Revenue for Q1 2017 was 58%, compared to 63% in Q1 2016. The decrease in our gross margin percentage is reflective of the change in the makeup of the product portfolio which now includes products with lower margins than in the prior year period as well as the impact of a stronger US dollar on the purchase of certain goods billed in USD. Once we have transitioned to more cost effective Euro denominated manufacturers over the next 6 to 12 months, the gross margin percentage is expected to improve substantially.

Operating Income

Operating loss for Q1 2017 was $3.7 million, compared to operating income of $0.3 million for Q1 2016. The decrease in operating income is primarily attributable to foreign exchange losses of $3.7 million recorded in Q1 2017, compared to foreign exchange gains of $0.6 million realized in Q1 2016, resulting in a $4.3 million negative impact on operating income. We also realized increased amortization expenses ($8.9 million for Q1 2017, compared to $7.4 million for Q1 2016), and increases in both general and administrative expenses as well as selling and marketing expenses resulting from our expanded product portfolio and related expanded operations. These increases were overall matched by the increase in gross margin in Q1 2017 over Q1 2016.

Finance Costs

Finance costs increased to $2.2 million in Q1 2017 from $0.95 million in Q1 2016 reflecting our increased debt as a result of the borrowings under our Amended and Restated Credit Facility that relate to our acquisitions of the nitrates portfolio from UCB and the women’s products portfolio from Sanofi in Q2 2016.

Income Tax Expense

Income tax expense increased to $0.5 million in Q1 2017 from $0.1 million in Q1 2016 as a result of our expanded product portfolio and taxable income as well as the recognition in Q1 2017 of a current tax provision relating to an income tax liability with respect to the payment of dividends on our preferred shares.

Net Loss

Net loss for Q1 2017 increased to $6.3 million ($0.05 per share, basic and diluted), compared to a net loss of $0.9 million ($0.01 per share, basic and diluted) for Q1 2016. The increased loss is attributable to our decreased operating income combined with higher borrowing costs to support an expanded portfolio and increased income tax expenses.

EBITDA and Adjusted EBITDA

EBITDA decreased to $5.3 million for Q1 2017 from $7.5 million for Q1 2016, representing a year-over-year decrease of 29%. The decrease in EBITDA was largely attributable to increased foreign exchange losses in Q1 2017. Adjusted EBITDA increased to $10.8 million for Q1 2017 from $8.5 million for Q1 2016, representing a year-over-year increase of 27%. The increased Adjusted EBITDA is reflective of our expanded portfolio and execution of our strategy.

Product Portfolio Revenue

Revenue from our product portfolio for Q1 2017 is presented below. Revenue for products that are in a transition phase pending the transfer of marketing authorizations are presented in our financial statements on a net revenue basis and accordingly reflect revenue net of cost of goods and selling expenses. Below we present and discuss revenue for these products on Gross Basis Revenue basis and have included a table that reconciles Gross Basis Revenue with revenue on a net revenue basis, as reported in our financial statements. See above under “Non-IFRS Financial Measures” for a discussion of the definition of Gross Basis Revenue.

Product revenue is summarized in the table below for Q1 2017.

	Three months ended December 31, 2016
	2016			2015
	Revenue as Reported	Add: COGS and Selling Expense included in Revenue	Gross Basis Revenue1	Revenue as Reported	Add: COGS and Selling Expense included in Revenue	Gross Basis Revenue1
Enablex/Emselex	5,603,912	-	5,603,912	7,794,298	-	7,794,298
Sintrom	5,620,396	-	5,620,396	5,258,262	1,630,164	6,888,426
Nitrates  portfolio	7,931,656	4,859,808	12,791,464	-	-	-
Sanofi portfolio	3,095,895	-	3,095,895	-	-	-
Salagen	2,035,699	-	2,035,699	1,611,363	390,737	2,002,100
Vancocin	606,196		606,196	836,796	-	836,796
Estraderm	1,175,050	-	1,175,050	425,132	317,044	742,176
Total Revenue	26,068,804	-	30,928,612	15,925,851	-	18,263,796
Cost of Goods Sold	8,119,768	4,859,808	12,979,576	4,621,987	2,337,945	6,959,932
Gross Margin	17,949,036	-	17,949,036	11,303,864	-	11,303,864
Gross Margin (%)	69%		58%	71%		62%

Enablex

We completed the acquisition of Enablex from Novartis in 2013 and sales of Enablex are no longer subject to any transitional agreement.

Gross Basis Revenues attributable to Enablex for Q1 2017 decreased to $5.6 million from $7.8 million for Q1 2016, representing a decrease of 28%. Enablex sales in Q1 2017 reflect the full impact of the 60% reduction in the maximum reimbursable price for Enablex in Germany, the product’s largest market, which became effective April 1, 2016. The decrease in price was partially off-set by volume increases for Enablex in Germany, as anticipated. Sales in Czech Republic increased substantially in anticipation of an opportunity resulting from the departure of a competitor’s product from the market. New launches of Emselex in other Central and Eastern European countries, continued growth in the UK and Portugal, and market share gains in Germany are anticipated to generate incremental sales over the course of fiscal 2017.

Sintrom

We completed the acquisition of Sintrom in September 2014. Sales of Sintrom in Q1 2017 were not subject to any transitional agreement as all market authorizations had been transferred to us by the end of FY 2016.

Gross Basis Revenue for Sintrom decreased to $5.6 million for Q1 2017 from $6.9 million for Q1 2016, representing a decrease of 18%. Wholesaler inventory levels at FY 2016 year-end were above normal levels driven by increases in safety stock in anticipation of transferring manufacturing to our CMO. Q1 2017 sales Sintrom reflect the normalizing of this inventory as wholesalers released approximately two weeks of inventory as the transfer of manufacturing to our new CMOs, which is the first phase of the Sintrom tech transfer, concludes. We expect Sintrom® inventories to continue to fluctuate over the course of 2017 as the remaining phases of technology transfer are implemented.

Nitrates Portfolio

We completed the acquisition of the nitrates portfolio from UCB on February 4, 2016. Q1 2017 sales included Merus sales to customers and UCB sales to customers for Marus’ account in accordance with the transition services agreement entered into with UCB on closing the acquisition. While in some territories we continue to require these transition services, in many we have shifted to selling directly, thus net revenue reflects a combination of sales of nitrates on a gross basis and a net basis. It is anticipated that the significant majority of these transitions will have been completed by the end of Q2 2017, with the result that almost all sales will be effectively conducted by Merus and recorded at full sales value for periods following Q2 2017.

Gross Basis Revenue from the newly-acquired nitrates portfolio was $12.8 million for Q1 2017 compared with nil in Q1 2016. Nitrate revenues retracted as some wholesalers worked through additional product purchased in fiscal Q4 2016 as part of the transfer of UCB affiliate inventory directly to Merus customers. Cost of goods were elevated in FY 2016 as the Company worked through inventory available at the time of acquisition and which was required to be purchased at a higher transfer price as part of the acquisition agreement. The higher cost inventory had largely been depleted by Q1 2017 and newly produced goods began being purchased at a lower cost during Q4 2016. As a result, Q1 2017 largely reflected lower cost inventory.

Sanofi Portfolio

We completed the acquisition of the women’s health portfolio from Sanofi on March 7, 2016 for which there is a short transitional services arrangement which allowed us to record revenues on a gross basis in the financial statements from the date of acquisition.

Revenues from the Sanofi product portfolio during Q1 2017 were $3.1 million compared with nil in Q1 2016. Revenues were higher than anticipated during the quarter as demand remains robust.

Salagen

We completed the acquisition of Salagen from Novartis on May 21, 2015. All sales were initially made subject to a transition services agreement. As a result of the transfer of all of the marketing authorizations prior to the end of FY 2016, all revenues from Salagen during Q1 2017 were recorded on a net revenue basis.

Gross Basis Revenue for Salagen was $2.0 million for Q1 2017, compared to $2.0 million for Q1 2016. The small increase relates to wholesaler buying patterns and the availability of stock in the supply chain.

Estraderm

We completed the acquisition of Estraderm from Novartis on May 21, 2015. All sales were initially made subject to a transition services agreement. As a result of the transfer of all of the marketing authorizations prior to the end of FY 2016, all revenues from Estraderm during Q1 2017 were recorded on a net revenue basis.

Revenues from Estraderm during Q1 2017 on a Gross Basis Revenue basis were $1.2 million, compared to $0.7 million for Q1 2016. Results for Q1 2017 are higher than usual due to the filling of backorders resulting from limited stock outs in FY 2016 as well as increased sales volumes resulting from the stock out of competing products in Spain and Australia during Q1 2017.

Vancocin

We completed the acquisition of Vancocin in 2012. Sales of Vancocin are not subject to a transition services agreement and are all recorded on a gross basis.

Revenues attributable to Vancocin for Q1 2017 declined to $0.6 million from $0.8 million for Q1 2016. The decrease in revenue from Vancocin is the result of both an increase in our estimated returns provisions on current sales and declines in sales volumes over the prior year period as the market competition matures and as there have been no recent significant outbreaks of C. difficile.

Operating Expenses

	Three months ended December 31
	2016	2015
Selling & Marketing
Marketing and promotion	337,498	159,185
Regulatory and pharmacovigilance	3,728,856	790,590
Consulting and other selling	-	305,605
Total	4,066,354	1,255,380
General & Administrative
Salaries, bonus, and benefits	1,563,060	602,617
Professional fees	790,241	475,077
Legal settlement costs	998,176	-
Business development	158,863	54,716
Exchange and filing fees	57,148	32,416
Travel expenses	79,655	85,402
Rent and premises expenses	166,879	46,557
Other	217,092	216,424
Total	4,031,114	1,513,209

Selling and Marketing Expense

Merus incurred selling and marketing expenses of $4.1 million for Q1 2017, compared to $1.3 million for Q1 2016. Selling and marketing expenses include all costs related to marketing, promoting and selling our products. Certain amounts in the prior period have been reclassified in order to better reflect true selling and marketing costs and cost of goods sold to improve comparability. Selling and marketing expenses are higher in the current period primarily due to an increase in marketing and promotion expenses in connection with recent launches of Emselex in new territories and increased expenses related to the on-going transfer and integration of pharmacovigilance activities to a new service provider for the Company’s entire product portfolio, excluding Vancocin.

General and Administrative Expense

General and administrative expenses for Q1 2017 were $4.0 million, compared to $1.5 for Q1 2016 and do not include non-cash share-based compensation. General and administrative expenses increased in Q1 2017 in comparison to Q1 2016 primarily due to the one-time Factive legal settlement charges of $1.0 million, as explained previously, increased headcount to support an expanded portfolio, increased investment in business development, and the scaling-up of operations due to a larger product portfolio.

Share-based Compensation

Share-based compensation costs decreased to $0.9 million for Q1 2017 from $1.1 million for Q1 2016 primarily due to a decrease in the estimated fair value of the option and PSU awards granted during Q1 2017.

Amortization of Intangible Assets

Amortization expense of intangible assets for Q1 2017 increased to $8.9 million from $7.4 million for Q1 2016. The increase in amortization is mainly due to the additions of the UCB and Sanofi product portfolios in Q2 2016, offset by a decrease resulting from an increase in the estimated remaining useful life of the Company’s products, as discussed under “Critical Accounting Policies - Useful Lives of Property, Equipment and Intangible Assets”.

Foreign Exchange Losses (Gains)

Foreign exchange losses were $3.7 million for Q1 2017, compared to a foreign exchange gain in Q1 2016 of $0.6 million. The loss in Q1 2017 was primarily due to the depreciation in value of the Euro between the end of Q4 2016 (EUR:CAD of 1.4741) versus the end of Q1 2017 (EUR:CAD of 1.4169) and its impact on the Company’s net balance sheet position in this currency. Foreign currency gains in Q1 2016 were attributable to the appreciation of the USD dollar and Euro compared to the Canadian dollar.

Interest Expense

Interest expense increased to $2.2 million for Q1 2017 from $0.95 million for Q1 2016 as a result of our increased debt in Q1 2017 compared to Q1 2016. The higher interest charges relate to the higher average outstanding debt balance Q1 2017 in connection with the loans under the Amended and Restated Credit Agreement that was executed in February 2016, as well as increased expense for the amortization of capitalized transaction costs of the new loan.

Derivative Losses

Derivative gains of $0.1 million were recorded in Q1 2017, primarily related to the favourable mark-to-market revaluation of the interest rate swap entered into in May 2016 in connection with our Euro-denominated debt, offset by the settlement of interest rate swap payments. Derivative losses of $0.1 million were recorded in the Q1 2016 primarily due to the settlement and mark-to-market of unfavourable interest rate swaps and Euro foreign exchange hedges.

SUMMARY OF QUARTERLY RESULTS

$ millions unless noted	Q1 2017	Q4 2016	Q3 2016	Q2 2016	Q1 2016	Q4 2015	Q3 2015	Q2 2015
Total revenues as reported	26.07	29.80	25.66	19.70	15.93	16.14	9.51	12.68
Total Gross Basis Revenue1	30.93	34.35	32.57	26.22	18.26	21.38	13.68	16.90
Gross margin2	17.95	18.88	16.30	13.49	11.30	11.90	8.56	11.12
Net income (loss)	(6.32)	(0.07)	(5.05)	(3.43)	(0.92)	0.02	(1.81)	1.76
Earnings (loss) per share (in $'s):
Basic	(0.05)	(0.00)	(0.04)	(0.03)	(0.01)	0.00	(0.03)	0.03
Diluted	(0.05)	(0.00)	(0.04)	(0.03)	(0.01)	0.00	(0.03)	0.03
Total assets	360.84	375.38	368.92	388.90	258.32	263.98	246.66	188.20
Total long-term financial liabilities	141.43	155.01	158.81	171.18	68.80	72.66	76.51	80.35
EBITDA3	5.32	13.38	7.76	8.88	7.57	7.15	5.84	9.42
Adjusted EBITDA3	10.85	11.62	11.88	11.04	8.54	9.31	6.36	9.39

¹ Gross Basis Revenues - Non-IFRS Financial Measures - see definition under "Overall Performance"

² Gross margin - prior period amounts have been restated to conform with current period presentation

³ EBITDA and Adjusted EBITDA - Non-IFRS Financial Measures - see definition under "Overall Performance"

During the periods presented in the table above, our business has undergone significant growth as a result of the product acquisitions we have completed. Our results of operations for Q2 2015 reflect sales of our Enablex, Vancocin, and Sintrom products, whereas our result of operations for Q1 2017 reflect Enablex, Sintrom, our nitrates product portfolio, our Sanofi product portfolio, Salagen, Estraderm and Vancocin. This expansion in our product portfolio has resulted in the significant increase in our revenues over this eight quarter period, and a corresponding significant increase in both our assets and our liabilities.

Our revenues in Q2 2015 reflected a full quarter of our recently acquired Sintrom product in addition to our Enablex and Vancocin products. We reported our initial positive net income of $1.8 million in Q2 2015, primarily due to an increased share of in-market Enablex revenue due to the expiration of a legacy marketing agreement. Revenue dipped somewhat in Q3 2015 mainly due to the timing of inventory shipments which resulted in lower recognized sales for the period.

Revenue rebounded in Q4 2015 and the Q1 2016 primarily as a result of the revenue from Sintrom shifting from a net revenue basis to a Gross Basis Revenue basis as the process of transferring marketing authorizations from Novartis to the Company continued.

We acquired the nitrates portfolio from UCB and the women’s health portfolio from Sanofi in Q2 2016. These acquisitions significantly increased our assets and liabilities as at March 31, 2016 in comparison to December 31, 2015. The initial revenues from these newly acquired products also increased our revenue in Q2 2016.

Our revenue has continued to increase during Q3 2016 and Q4 2016 in comparison to Q2 2016 as these quarters reflected the full period of operations for the products acquired from UCB and Sanofi and most of the Sintrom, Salagen, and Estraderm revenue was now being reported on a gross basis.

Revenues increased again in Q4 2016 due to the transfer of commercial responsibility for certain territories to Merus for the nitrates portfolio previously being administered through the UCB transition arrangement. This allowed for revenue to be recorded directly by Merus, but also resulted in slightly elevated levels of sales to ensure a smooth transition to Merus’ commercial partners. Further, certain Sintrom distribution channels were loaded in preparation for the upcoming manufacturing transfer to our new CMO.

The overall decrease in revenues from Q4 2016 to Q1 2017 is reflective of the normalization of inventory levels at the customer level as a result of loading that occurred during Q4 2016 as well as the impact of certain customer ordering patterns.

Consistent with the increase in our assets resulting from product acquisitions, our amortization expenses have increased significantly over prior quarters as we are required to amortize the acquisition cost of product rights over their estimated remaining useful lives. This increase in amortization expense has had a significant impact on our earnings, with the result that our net loss has increased marginally notwithstanding the significant growth in our revenue. For the fiscal year 2017, we have reviewed our estimated remaining useful lives on an asset by asset basis and have revised them accordingly to better reflect our expectations regarding these assets.

Seasonality

Merus’ product lines are generally not susceptible to seasonal fluctuations. Historical sales trends have not indicated that any of our products have seasonal variations that would materially impact quarterly revenue trends.

LIQUIDITY AND CAPITAL RESOURCES

We currently manage our capital structure and make adjustments to it based on, amongst other things, the cash resources expected to be generated to support our future business plans. We currently have three principal sources of capital, namely (i) cash flows from our operations, (ii) our debt facilities, and (iii) potential future equity financings.

We currently generate significant positive cash flows from operations and these cash flows are used to retire our long-term debt obligations. We may raise additional equity capital, as required, to pursue the acquisition of additional pharmaceutical products. In addition, while existing debt will be retired using cash flows generated from current operations, new debt may be obtained to pursue the acquisition of new pharmaceutical assets. We review our capital management approach on an ongoing basis in conjunction with external factors and believe that our current approach is optimal at present. If additional sources of capital are required and are not available or are not available at economically reasonable terms, we will need to assess alternatives including expense reductions and the sale of existing assets.

Over the next twelve months, our plan is to use our operating cash flow to satisfy our short-term debt obligations, while continuing to pursue strategic acquisitions. In February 2016, in conjunction with our product portfolio acquisitions from UCB and Sanofi, we refinanced our credit facility to a new Euro-denominated five-year term loan. This loan represented approximately $120 million in new capital. In addition, in March 2016, we completed a bought-deal financing of special warrants that resulted in gross proceeds of $27 million. These new funds, along with a portion of our cash on hand, were used to acquire the two product portfolios from UCB and Sanofi for a total of approximately $175 million.

We continue to evaluate both legacy and growth medicine acquisitions. We anticipate that any near term acquisitions will be funded by additional debt and/or equity financings. We currently do not have any arrangements in place for new debt or equity financings and there is no assurance that we will be able to obtain new debt or equity financings at attractive terms when required.

Cash and Working Capital

Merus had cash and cash equivalents of $4.0 million as at December 31, 2016, compared to $3.2 million as at September 30, 2016.

We had a working capital deficit of $10.2 million as at December 31, 2016, compared to a working capital deficit of $13.7 million as at September 30, 2016. The decrease in working capital deficit is primarily attributable to a decrease in long term debt due within one year to $30.5 million as at December 31, 2016 from $36.1 million as at September 30, 2016. Our working capital deficit as at December 31, 2016 is primarily attributable to the current portion of our long-term debt in the amount of $30.5 million which is repayable under the Amended and Restated Credit Agreement, as further discussed below. As at December 31, 2016, excluding provisions and obligations related to the current portion of our long-term debt, we had working capital of $20.3 million compared to $22.5 million at September 30, 2016.

We plan to repay the principal and interest amounts due under the Amended and Restated Credit Facility using cash generated from operations. We believe that cash generated from operations will be sufficient to pay these principal amounts without any additional debt or equity financing required, although we may use our increased revolving credit facility, as discussed below, to bridge short-term cash flow requirements.

Amended and Restated Credit Agreement

Merus entered into the Amended and Restated Credit Agreement in February 2016 in connection with the product acquisitions completed in the second quarter of 2016. The credit facilities under the Amended and Restated Credit Agreement include a $10 million senior secured revolving credit facility and a $170 million senior secured term facility. Advances under the senior secured term facilities are denominated in Euros and are repayable over a five-year term, with equal quarterly repayments of the principal advanced. The applicable interest rates of loans advanced under the credit facilities are determined by reference to the ratio of our senior funded debt to our EBIDTA in accordance with the terms of the Amended and Restated Credit Agreement. All amounts under the senior secured term facilities were advanced in the second quarter of 2016.

Finally, under the Amended and Restated Credit Agreement, we repaid the $60.0 million owing under our Original Credit Agreement, entered into in September 2014 in connection with our acquisition of Sintrom®.

On December 30, 2016, we secured interim arrangements with the creditors under the Amended and Restated Credit Agreement to temporarily provide additional working capital. These arrangements include (i) a temporary increase in the revolving credit facility from $10 million to $15 million for calendar 2017 only, (ii) extension of certain covenants at 2016 levels through 2017 to reflect the temporary increase in the revolving credit facility, and (iii) waiver of the excess cash flow sweep for FY 2016 only.

Our long term debt, inclusive of the current portion of long term debt due within one year and capitalized transaction costs, decreased to $131 million as at December 31, 2016 from $145 million as at September 30, 2016.

Our operating cash flow continues to be temporarily constrained as we build working capital, as required to reflect our expanded product portfolio, and we de-lever our debt.

Cash Provided by Operations

Cash provided by our operations was $4.9 million in Q1 2017 compared to $6.9 million in Q1 2016. This decrease was primarily due to costs associated with the expanded product portfolio and one-time Factive legal settlement costs, as well as higher interest rate expenses.

Cash Provided by Financing Activities

Cash used by financing activities in Q1 2017 was $3.9 million, compared to $4.0 million in Q1 2016. The Q1 2017 financing activities are comprised of the quarterly repayment of our term loan, offset by a draw on the operating line to finance short-term working capital needs. The Q1 2016 financing activities are entirely comprised of the quarterly repayment required under our old credit facility agreement.

Cash Used in Investing Activities

Cash used in investing activities was $0.24 million in Q1 2017 compared to $0.27 million in Q1 2016.

Fiscal 2017 Outlook

The Company reiterates that its FY 2017 Adjusted EBITDA guidance, without consideration of new acquisitions, is expected to be in the range of $44 to $48 million. We expect to have a significantly stronger second half in FY 2017, where approximately 55% of annual Adjusted EBITDA is expected. Our FY 2017 guidance reflects a full year of our base products and an expected $4 million savings from the Sintrom tech transfer, building in phases to a level of approximately $2 million quarterly savings by the end of fiscal Q4 2017. As well, a reduction in ongoing operating expenses (primarily in the regulatory and compliance area) is anticipated to be realized in the second half of FY 2017, with some one-time costs incurred in the first half of FY 2017. We have reached a major milestone in the execution of our technology transfer and started shipping Sintrom® product produced by our contract manufacturer (with Novartis manufactured active pharmaceutical ingredient) in Spain, the largest Sintrom® market. As Merus realizes the benefit of these profit enhancing initiatives, fiscal Q4 2017 Adjusted EBITDA is expected to be approximately 25% higher than that of fiscal Q1 2017.

We anticipate FY 2017 will be a transition year for Merus, and our focus will be on operational effectiveness: optimizing sales, streamlining expenses, assessing our debt structure, and enhancing systems and processes.

As we continue to pay down our debt in fiscal 2017 in accordance with the provisions of the term loan under our Amended and Restated Credit Facility, we anticipate that the ratio of our net debt (being the current and long-term portions of our debt, less cash and short term investments) to Adjusted EBITDA, as calculated on a 12 month rolling forward basis, will drop to 2.0 within 12 months.

Our earnings guidance is not predicated on any built-in product price increases. Guidance also does not include any reductions in sales from any new generic or other branded product competition. We have included in our guidance allowance for some price impact in smaller markets for our Enablex product as a follow-on to the price reduction determination in Germany.

Adjusted EBITDA for Q1 2017 was $10.8 million and met management’s expectations.

CRITICAL ACCOUNTING POLICIES

We consider the following to be our critical accounting policies:

Revenue recognition and estimated product returns

Revenue from product sales, including shipments to distributors, is recognized when Merus has transferred to the customer the significant risks and benefits of ownership or future obligations with respect to the product, and it is probable that the economic benefits associated with the transaction will flow to the Company and the amount of revenue can be measured reliably. Revenue from product sales is recognized net of estimated sales discounts, credits, returns, rebates and allowances.

In connection with certain acquisitions, the Company may enter into a form of transition service arrangement whereby the seller of the asset or business will continue to perform certain activities to facilitate the seamless and efficient transfer of the products. Upon the recent acquisitions of the nitrates portfolio from UCB, the Company entered into a transition agreements with UCB to provide distribution, regulatory and other supply chain functions for a period time post-sale, until the marketing authorizations for the products transferred to the Company. During the transition period, UCB provides the Company with a monthly reconciliation of revenues, costs of goods and other related expenses, for which the Company then bills UCB. With the acquisitions of Sintrom, Salagen and Estraderm, we entered into a transition services and supply agreement with the vendor, Novartis. The agreements required that Novartis continue to manufacture, distribute, and promote the product until we obtained the necessary marketing authorizations to allow it to take over these functions as principal. Novartis provided us a monthly reconciliation of revenues, cost of goods, and marketing and selling expenses for which we then billed Novartis for the net amount receivable. In this transition agreement periods, we rely on the financial information provided by the vendor to estimate the amounts due under this agreement. Based on the terms of this arrangement and the guidance per IAS 18 regarding agency relationships, for the period of these arrangements, revenues relating to the products were recorded on a net basis in the statement of operations, net of cost of goods and marketing and selling expenses.

Our return policy is limited to damaged or expired product. The return allowance is determined based on analysis of the historical rate of returns and current market conditions, which is applied directly against sales.

Share-based compensation

From time to time, Merus grants options and performance share units (PSU’s) to directors, officers, employees and non-employees to purchase common shares. We account for these stock options using the fair-value method. Share-based payments, equal to the fair value of the options on the date of grant, are recognized in the statement of operations, with an offsetting credit to equity reserves, for stock options granted to employees, officers and directors over the period during which the related options vest. Share-based payments are recognized in the statement of operations, with an offsetting credit to equity reserves, for options granted to non-employees based on the fair value of the services received. Consideration paid upon exercise of stock options, along with the applicable amount of equity reserves, is credited to share capital.

Intangible assets

Intangible assets include all costs incurred to acquire licensing and distribution agreements, product rights and patents. Intangible assets are recorded at cost less accumulated amortization and accumulated impairment losses and are amortized on a straight-line basis over their estimated useful life of 2 to 15 years. Costs incurred with respect to the transfer of manufacturing know-how, methods, and technology from the original manufacturer to the Company’s own manufacturing partner are capitalized as incurred under the criteria of internally generated intangible assets as defined by IAS 36 - Intangible assets. Such costs are only amortized once commercial production with the new manufacturing partner commences. Management has estimated the useful life based on industry data of similar products and patents. We conduct an annual assessment of the residual balances, useful lives and amortization methods being used for intangible assets and any changes arising from the assessment are applied prospectively.

Business combinations and goodwill

Business combinations are accounted for using the acquisition method. The cost of an acquisition is measured as the aggregate of the consideration transferred, measured at the acquisition date fair value. Acquisition costs incurred are expensed and included in acquisition costs.

Goodwill represents the price paid for acquisitions in excess of the fair market value of net tangible and identifiable intangible assets acquired. Goodwill is carried at cost, less impairment losses if any. Goodwill is tested for impairment at the end of each fiscal year or if events or changes in circumstances indicate a potential impairment. Determining whether goodwill is impaired requires an estimation of the recoverable amount of the cash generating units (“CGUs”) to which goodwill has been allocated.

For the purpose of impairment testing, goodwill acquired in a business combination is allocated to each of the CGUs, or groups of CGUs, that is expected to benefit from the synergies of the combination. Each unit or group of units to which the goodwill is allocated represents the lowest level within the entity at which the goodwill is monitored for internal management purposes.

Foreign currency translation

(i)        Functional and presentation currency

Items included in the financial statements of each of the Company’s entities are measured using the currency of the primary economic environment in which the entity operates (the “functional currency”). The consolidated financial statements of the Company are presented in Canadian dollars (“CAD”), which is the parent Company’s functional and presentation currency. The functional currency of Merus Labs Luxco S.a R.L., Merus Labs Luxco II S.a R.L., and Merus Labs Netherlands BV is Euros. The functional currency of Merus Pharma Inc. and ECG Holdings (US) Inc. is Canadian dollars.

(ii)        Transactions and balances

Foreign currency transactions are initiated by the Company’s entities at their respective functional currency using the exchange rates prevailing at the date of the transaction. At each statement of financial position date, monetary assets and liabilities are translated using the period-end foreign exchange rate. Non-monetary items that are measured in terms of historical cost in a foreign currency are translated using exchange rates as at the dates of the initial transactions. Non-monetary items measured at fair value in a foreign currency are translated using the exchange rates at the date when acquired. All gains and losses on translation of these foreign currency transactions are included in the statement of operations.

(iii)       Company’s subsidiaries

On consolidation the assets and liabilities of foreign operations are translated into CAD at the rate of exchange prevailing at the reporting date and their statement of operations are translated at the average exchange rates prevailing during the period. The exchange differences arising on translation for consolidation are recognized in other comprehensive income. On disposal of a foreign operation, the component of other comprehensive income relating to that particular foreign operation is recognized in the consolidated statement of operations.

Impairment of non-financial assets

At the end of each reporting period, we review the carrying amounts of our property and equipment, intangible assets and goodwill to determine whether there is an indication that those assets have suffered an impairment loss. If any such indication exists, the recoverable amount of the asset is estimated in order to determine the extent of the impairment loss. In addition, goodwill, intangible assets with indefinite useful lives and intangible assets not yet available for use, if any, are tested for impairment annually.

An impairment loss is recognized when the carrying amount of an asset, or its CGU, exceeds its recoverable amount. A CGU is the smallest identifiable group of assets that generates cash inflows that are largely independent of the cash inflows from other assets or groups of assets.

The recoverable amount is the greater of the asset’s or CGU’s fair value less costs to sell (“FVLCTS”) and value in use (“VIU”). In assessing VIU, the estimated future cash flows are discounted to their present value using a pre-tax discount rate that reflects current market assessments of the time value of money and the risks specific to the asset or CGU. In determining FVLCTS, a post-tax discounted cash flow model is used. For an asset that does not generate largely independent cash inflows, the recoverable amount is determined for the CGU to which the asset belongs. If the recoverable amount of the asset or CGU is less than its carrying amount, an impairment loss is recognized immediately in the statement of operations.

Other than goodwill, where an impairment loss subsequently reverses, the carrying amount of the asset is increased to the revised estimate of its recoverable amount to the extent that the increased carrying amount does not exceed the carrying amount that would have been determined had no impairment loss been recognized for the asset in prior years. Goodwill impairment losses are not reversed.

Critical judgements

The following are the critical judgements, apart from those involving estimations (see below), that we have made in the process of applying our accounting policies and that have the most significant effect on the amounts recognised in the consolidated financial statements.

Acquisition accounting

Management has exercised judgement in determining that the product acquisitions of the nitrates portfolio from UCB and the women's health portfolio from Sanofi were each acquisitions of a business. In addition, management has exercised judgement in determining that the product acquisitions of Salagen and Estraderm were asset acquisitions. Management considered the guidance and definitions per IFRS 3 and IAS 38 in making these determinations. These transactions have been recorded in the consolidated financial statements based on management’s assessment of fair value for the acquired assets and liabilities.

Functional currency

Management has exercised judgement in selecting the functional currency of each of the entities that it consolidates based on the primary economic environment in which the entity operates and in reference to the various indicators as provided by IAS 21 - The effects of changes in foreign exchange rates. Our consolidated financial statements are presented in Canadian dollars (“CAD”), our functional and presentation currency.

Use of estimates

In preparing the consolidated financial statements in accordance with IFRS, management is required to make estimates and assumptions that affect the reported amount of assets, liabilities, and the disclosure of contingent liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates used in the consolidated financial statements and such differences could be material. Significant estimates include:

• the allowance for inventory obsolescence;

• estimates for product returns

• allocation of the purchase price and estimates of fair value for the acquired assets and liabilities;

• the estimated useful lives of property and equipment and intangible assets;

• impairment of financial and non-financial assets;

• valuation of deferred tax assets and liabilities;

• the valuation of warrants and share-based compensation expense; and

• the calculation of effective interest on its long-term debt based on the most reliable estimates of required repayments

Significant estimates

The following are the key assumptions concerning the future, and other key sources of estimation uncertainty at the end of the reporting period, that have a significant risk of causing a material adjustment to the carrying amounts of assets and liabilities within the next financial year.

Inventory obsolescence

The Company reviews the net realizable value of its inventory. The Company has determined that there are adequate sales to support the carrying amount for all inventories as at September 30, 2016. In addition, management reviews specific product and industry experience with returns in assessing if a write-down is required.

Estimated product returns

Revenue from product sales is recognized net of estimated sales discounts, credits, returns, rebates and allowances. The Company’s return policy is limited to damaged or expired product. The return allowance is determined based on an analysis of the historical rate of returns, industry return data, and current market conditions, which is applied directly against sales.

Allocation of the purchase price and estimates of fair value for the acquired assets and liabilities

A preliminary assessment of the fair value of all assets and liabilities acquired via business combinations and product acquisitions is performed based on all current available information. Management updates the estimated fair value as information becomes available, support from third party market data becomes available, and where necessary, third party independent valuations are obtained. Management is ultimately responsible for the allocation of the purchase price and estimates of fair value for the acquired assets and liabilities.

Impairment of financial and non-financial assets

Financial Assets

At the end of each fiscal quarter, Merus determines whether there is objective evidence that a financial asset or group of financial assets is impaired.

If there is objective evidence that an impairment loss has occurred on an unquoted or not actively traded equity instrument that is not carried at fair value (because its fair value cannot be reliably measured), the amount of the loss is measured as the difference between the asset’s carrying amount and the present value of estimated future cash flows discounted at the current market rate of return for a similar financial asset and is recognized in profit or loss for the period. Reversals of impairment losses on assets carried at cost are not permitted.

For financial assets carried at amortized cost, the amount of the loss is measured as the difference between the asset’s carrying amount and the present value of estimated future cash flows (excluding future credit losses that have not been incurred) discounted at the financial asset’s original effective interest rate (i.e. the effective interest rate computed at initial recognition).

Objective evidence of impairment of financial assets carried at amortized cost exists if the counterparty is experiencing significant financial difficulty, there is a breach of contract, concessions are granted to the counterparty that would not normally be granted, or it is probable the counterparty will enter into bankruptcy or a financial reorganization.

Non-Financial Assets

Determining whether goodwill is impaired requires an estimation of the recoverable amount of the cash generating units (“CGUs”) or groups of CGUs to which goodwill has been allocated. The determination of recoverable amount requires us to estimate the future cash flows expected to arise from these CGUs and a suitable discount rate in order to calculate the recoverable amount of the CGUs. If the recoverable amount of the CGUs is less than its carrying amount, an impairment loss is recorded. Merus currently has no goodwill.

At the end of each reporting period, the Company reviews property and equipment and intangible assets for indicators of impairment. If any such indication exists, the recoverable amount of the asset is estimated in order to determine the extent of the impairment loss, if any. Where it is not possible to estimate the recoverable amount of an individual asset, the assets are then grouped together into a CGU and a recoverable amount is estimated for that CGU. As at September 30, 2016, no indicators of impairment were identified.

Useful lives of property, equipment and intangible assets

Merus reviews the estimated useful lives of property, equipment and intangible assets at the end of each year, with the effect of any changes in estimates being accounted for on a prospective basis.

Depreciation of property, equipment, and computer software is calculated using the straight-line method and amortization of intangible assets, excluding computer software, is calculated using the declining balance method to allocate their cost their residual value over their estimated useful lives, as follows:

•	Furniture, fittings and computer equipment	3 - 5 years
•	Leasehold improvements	Over the term of the lease
•	Manufacturing equipment	5 to 10 years
•	Computer software	3 to 7 years
•	Product rights	2 - 15 years
•	Product patents	Remaining economic life of patent

During the three months ended December 31, 2016, Management reviewed the amortization period and method applied to the Company’s product rights. It was determined that the amortization method previously being applied (straight-line) was not reflective of the erosion pattern of these assets’ cash flows. Further, the amortization period for certain product rights were revised to better reflect Management’s best estimate of the remaining useful life of these assets as of the beginning of the fiscal year. As a result of this change in estimate, the amortization expense for the three months ended December 31, 2016 was approximately $1.3 million lower than what would have been recorded under the previous method and period of amortization.

Valuation of deferred tax assets and liabilities

The Company estimates the probability that taxable profits will be available against deductible temporary differences can be utilized and thus give rise to deferred tax assets. The Company has reviewed the expected profitability and determined that no deferred tax asset should be recognized at this time.

Valuation of warrants and share-based compensation expense

The Company estimates the fair value of warrants and share options issued for employment services based on the Black Scholes option-pricing model for warrants and share options with a service condition. These methods of valuation, which require management to use certain assumptions regarding inputs used, were applied to the equity transactions during the year.

The Company estimates the fair value of performance share units (PSUs) for employment services based on the market price of the shares on the date of the grant.

Estimation of effective interest rate on debt

The Company estimates the effective interest rate on any debt obligations based on the total financing costs incurred and the agreed upon repayment schedule, including any repayments that may be contingent on future earnings (i.e. cash flow sweeps).

FINANCIAL RISK MANAGEMENT

The use of financial instruments can expose the Company to several risks, including market, credit and liquidity risks. Apart from the risks listed below, management is of the opinion that they are not exposed to any other significant risks. A discussion of the Company’s use of financial instruments and its risk management is provided below:

Liquidity Risk

Liquidity risk is the risk that the Company will not have sufficient cash resources to meet its financial obligations as they come due. The Company’s liquidity and operating results may be adversely affected if the Company’s access to the capital markets is hindered, whether as a result of a downturn in stock market conditions generally or related to matters specific to the Company. In order to mitigate this risk, the Company maintains a sufficient cash balance in order to satisfy short-term liabilities as they come due and actively pursues raising capital through various public and private financing mechanisms to satisfy longer term needs.

The table below analyzes the Company’s non-derivative financial liabilities into relevant maturity groupings based on the remaining period at the statement of financial position date to the contractual maturity date. The amounts disclosed in the table are the contractual undiscounted cash flows and do not include capitalized transaction costs.

	Years ended September 30
At December 31, 2016	2017	2018	2019	Thereafter
Operating line	$   9,000,000	$                    -	$                    -	$                    -
Senior Secured Facility	23,731,331	31,641,774	31,641,774	47,462,659
Accounts payable and       accrued liabilities	20,508,667	-	-	-
Income taxes payable	1,083,098	-	-	-
Total	$ 54,323,096	$ 31,641,774	$ 31,641,774	$ 47,462,659

	Years ended September 30
At September 30, 2016	2016	2017	2018	Thereafter
Operating line	$   5,000,000	$                    -	$                    -	$                    -
Senior Secured Facility	37,266,232	32,919,147	32,919,147	45,031,630
Accounts payable and accrued liabilities	15,875,494	-	-	-
Income taxes payable	635,891	-	-	-
Total	$ 58,777,617	$ 32,919,147	$ 32,919,147	$ 45,031,630

Currency Risk

The Company is subject to currency risk through its sales of products and services denominated in foreign currencies, purchases of inventory in US dollars and product acquisitions denominated in foreign currencies. As such, changes in the exchange rate affect the operating results of the Company. Dependent on the nature, amount and timing of foreign currency receipts and payments, the Company may from time to time enter into foreign currency derivative contracts to reduce its exposure to foreign currency risk as discussed in note 8. In February 2016, the Company entered into a Euro Facility to establish a natural hedge against its Euro sourced revenues, thus minimizing the need for foreign currency derivative contracts.

The following significant monetary financial assets and liabilities were denominated in foreign currencies at December 31, 2016 (U.S. dollar 1.3427, Euro 1.4169, British pound 1.6565, Swiss franc 1.3214) and September 30, 2016 (U.S. dollar 1.3117, Euro 1.4741, British pound 1.7069, Swiss franc 1.3531):

	December 31 2016	September 30 2016
Canadian Dollar Equivalent :
Denominated in US dollars	$     (1,300,837)	$     (1,631,182)
Denominated in Euros	(127,946,875)	(143,423,582)
Denominated in British pounds	4,925,894	5,121,046
Denominated in Swiss francs	1,451,323	431,128
Net (liabilities) assets denominated in foreign currencies	$ (125,773,141)	$ (139,502,589)

The following table shows the estimated sensitivity of the Company’s total comprehensive gain (loss) for the period ended December 31, 2016 from a change in foreign currencies with all other variables held constant as at September 30, 2016:

	Change in net after-tax	Change in net after-tax
Percentage change in	gain from % increase	loss from % decrease
foreign currencies	in foreign currencies	in foreign currencies
2%	$     (2,515,463)	$      2,515,463
4%	(5,030,926)	5,030,926
6%	(7,546,388)	7,546,388
8%	(10,061,851)	10,061,851
10%	(12,577,314)	12,577,314

Market Risk

Market risk is the risk that the fair value of, or future cash flows from, the Company’s financial instruments will significantly fluctuate because of changes in market prices. The value of the financial instruments can be affected by changes in interest rates, foreign exchange rates, and equity and commodity prices. The Company is not exposed to significant market risk given the low value of its investments.

Credit Risk

Some of the Company’s financial assets, including cash and cash equivalents and short-term investments are exposed to the risk of financial loss occurring as a result of default of a counterparty on its obligations to the Company. The Company may, from time to time, invest in debt obligations. The Company is also exposed, in the normal course of business, to credit risk from customer receivables. These amounts are continually monitored by management for collectability, and, in general, are lower risk as they are typically due from large institutions or multinational distributors.

Interest Rate Risk

Merus has significant current and long-term debt in the form of senior secured debt which currently bears interest at a floating interest rate of EURIBOR (0% floor) plus 4.5% and will incur greater interest expenses if the EURIBOR rate rises. Management has reduced this risk by entering into an interest rate swap arrangement as allowed for through facilities in its credit agreement. Interest rate swaps effectively fix the interest rate on the debt to which they are applied. At December 31, 2016, Merus had interest rate swaps applied to approximately 50% of its senior secured debt facility and it is management’s opinion that Merus is not exposed to significant interest rate risk at this time.

COMMITMENTS

Operating lease commitments

Merus has entered into operating lease agreements for office premises and equipment with minimum annual lease payments to expiry as follows:

	December 31, 2016
Less than 1 year	$      300,540
1 to 2 years	300,540
2 to 3 years	300,540
Thereafter	400,720
Total	$   1,302,340

OFF BALANCE SHEET ARRANGEMENTS

Merus had no off balance sheet arrangements as at December 31, 2016 and does not have any off balance sheet arrangements as at the date of this MD&A.

RELATED PARTY TRANSACTIONS

At December 31, 2016, there were no amounts owing to or from related parties. The remuneration of directors and other members of key management personnel are as follows:

	Three months ended December 31
	2016	2015
Salaries	$     480,449	$     501,147
Share based compensation	788,022	1,092,173
	$    1,268,471	$  1,593,320

DISCLOSURE CONTROLS AND PROCEDURES

Disclosure controls and procedures form a framework designed to provide reasonable assurance that information disclosed publicly fairly presents in all material respects the financial condition, results of operations and cash flows of the Company for the periods presented in this MD&A. The Company's disclosure controls and procedures framework includes processes designed to ensure that material information relating to the Company, including its consolidated subsidiaries, is made known to management by others within those entities to allow timely decisions regarding required disclosure.

The Company’s management, with the participation of its CEO and CFO is responsible for establishing and maintaining adequate internal control over financial reporting. The Company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with IFRS.

On October 1, 2016, the Company commenced processing all financial transactions on its new enterprise resource planning (ERP) system. This system replaces and improves upon the various system and process-based controls that were previously in place. There were no other changes to the Company’s internal controls over financial reporting during Q1 2017.

DISCLOSURE OF OUTSTANDING SHARE DATA

Common Shares

Merus’ authorized share capital consists of an unlimited number of common shares without par value. As at February 13, 2017 we had 117,345,148 common shares issued and outstanding.

Preference Shares

Merus is authorized to issue an unlimited number of preferred shares without par value. The preferred shares may be issued in series on such terms as determined by our Board of Directors in accordance with the special rights and restrictions as set out in our Articles. As of February 14, 2017, we had 10,000 Series A Preferred Shares issued and outstanding, each with a liquidation value of $1,000, for a total value of $10,000,000. The Series A Preferred Shares pay a dividend of 8% per annum, subject to adjustment if Merus does not redeem them after October 31, 2019. At any time at the option of the holder, these Series A Preferred Shares may be converted into common shares at a conversion price of $2.20 per share. The Series A Preferred Shares are redeemable at Merus’ option at any time after October 31, 2019. Merus can also redeem them at any time in the event of a change of control subject to the payment of a change of control premium.

Stock Options

We have 6,873,500 stock options outstanding as at February 13, 2017.

ADDITIONAL INFORMATION

Additional information about Merus is available on SEDAR at http://www.sedar.com.

Merus Labs International Inc.
Condensed Consolidated Interim Statements of Financial Position
(Unaudited)
(Expressed in Canadian dollars)
As at:			December 31			September 30
			2016			2016
Assets
Current assets
Cash and cash equivalents		$	3,979,691		$	3,213,564
Short-term investments			3,210			3,155
Trade and other receivables			31,315,927			28,597,219
Inventories			15,188,907			12,700,393
Prepaid expenses			1,111,341			302,010
			51,599,076			44,816,341
Non-current assets
Property and equipment	note 3		308,824			322,485
Intangible assets	note 2, 4		308,934,106			330,245,892
Total assets		$	360,842,006		$	375,384,718
Liabilities and Equity
Current liabilities
Operating line	note 7	$	9,000,000		$	5,000,000
Accounts payable and accrued liabilities			20,508,667			15,875,494
Income taxes payable			1,083,098			635,891
Derivative liabilities	note 5		669,877			837,584
Provisions	note 6		122,777			128,678
Long term debt due within one year	note 7		30,451,119			36,070,095
			61,835,538			58,547,742
Non-current liabilities
Provisions	note 6		122,777			128,679
Long term debt	note 7		101,029,656			108,994,126
Preferred shares	note 8		9,947,730			9,947,730
Total liabilities			172,935,701			177,618,277
Equity
Share capital	note 9		210,756,585			210,756,585
Equity reserve	note 9		40,005,857			39,146,155
Accumulated deficit			(77,048,068	)		(70,730,658	)
Accumulated other comprehensive income	note 18		14,191,931			18,594,359
Total equity			187,906,305			197,766,441
Total liabilities and equity		$	360,842,006		$	375,384,718

Commitments and contingencies (note 10)
Approved on behalf of the Board:
(signed)	(signed)
Tim Sorensen,	Dave Guebert,
Director	Director

The accompanying notes are an integral part of these unaudited condensed consolidated interim financial statements

Merus Labs International Inc.
Condensed Consolidated Interim Statements of Operations
(Unaudited)
(Expressed in Canadian dollars)
		Three months ended December 31
		2016			2015
Revenues		$	26,068,804		$	15,925,851
Cost of goods sold	note 17		8,119,768			4,621,987
Gross margin			17,949,036			11,303,864
Operating expenses:
Selling and marketing	note 17		4,066,354			1,255,380
General and administrative	note 10, 11, 17		4,031,114			1,513,209
Share-based compensation	note 9		859,702			1,092,173
Acquisition costs	note 2		—			352,319
Amortization of intangible assets	note 4		8,941,592			7,356,701
Depreciation	note 3		13,166			3,854
Foreign exchange losses (gains)			3,748,357			(570,697	)
			21,660,285			11,002,939
Operating (loss) income			(3,711,249	)		300,925
Finance costs	note 12		2,208,562			947,629
Derivative (gains) losses	note 5		(77,410	)		136,872
Investment loss			—			(117	)
Loss before income taxes			(5,842,401	)		(783,459	)
Income tax expense	note 13		475,009			131,561
Net loss for the period		$	(6,317,410	)	$	(915,020	)
Loss per share
Basic		$	(0.05	)	$	(0.01	)
Diluted		$	(0.05	)	$	(0.01	)
Weighted average number of common shares outstanding - basic			116,999,906			102,372,965
Weighted average number of common shares outstanding - diluted			116,999,906			102,372,965

The accompanying notes are an integral part of these unaudited condensed consolidated interim financial statements

Merus Labs International Inc.
Condensed Consolidated Interim Statements of Comprehensive Income (Loss)
(Unaudited)
(Expressed in Canadian dollars)
	Three months ended December 31
	2016			2015
Loss for the period	$	(6,317,410	)	$	(915,020	)
Other comprehensive (loss) income
Items that may be reclassified to income:
Currency translation differences		(4,402,428	)		1,346,011
Other comprehensive (loss) income for the period		(4,402,428	)		1,346,011
Total comprehensive (loss) income for the period	$	(10,719,838	)	$	430,991

The accompanying notes are an integral part of these unaudited condensed consolidated interim financial statements

Merus Labs International Inc.
Condensed Consolidated Interim Statements of Cash Flows
(Unaudited)
(Expressed in Canadian dollars)
	Three months ended December 31
	2016			2015
Operating activities
Net loss for the period	$	(6,317,410	)	$	(915,020	)
Adjustments for the following items:
Amortization of intangible assets		8,941,592			7,356,701
Depreciation		13,166			3,854
Finance costs		2,208,562			947,629
Income tax expense		475,009			131,561
Unrealized losses on foreign exchange		2,399,841			491,675
Share-based compensation		859,702			1,092,173
Change in fair value of derivative financial instruments		(167,707	)		(315,187	)
Interest paid		(2,068,724	)		(802,529	)
Net change in non-cash working capital balances:
Provisions		(11,803	)		(4,450	)
Trade and other receivables		(2,718,708	)		2,100,566
Prepaid expenses		(809,331	)		(159,888	)
Inventories		(2,488,514	)		83,290
Accounts payable and accrued liabilities		4,633,173			(3,149,161	)
Income taxes payable		(27,802	)		17,927
Net cash provided by operating activities		4,921,046			6,879,141
Financing activities
Proceeds from operating line draw		4,000,000			—
Repayment of long-term debt		(7,910,062	)		(4,000,000	)
Net cash used in financing activities		(3,910,062	)		(4,000,000	)
Investing activities:
Purchase of property and equipment		(3,408	)		—
Capitalized product and software development costs		(241,394	)		(266,829	)
Short-term investments		(55	)		(116	)
Net cash used in investing activities		(244,857	)		(266,945	)
Net change in cash and cash equivalents		766,127			2,612,196
Cash and cash equivalents, beginning of period		3,213,564			40,987,177
Cash and cash equivalents, end of period	$	3,979,691		$	43,599,373

The accompanying notes are an integral part of these unaudited condensed consolidated interim financial statements

Merus Labs International Inc.
Condensed Consolidated Interim Statements of Changes in Equity
(Unaudited)
(Expressed in Canadian dollars)
	Share capital		Equity reserve		Accumulated deficit			Accumulated other comprehensive income (AOCI)			Total equity
Balance, September 30, 2015	$	184,534,553	$	37,215,779	$	(61,271,614	)	$	20,318,732		$	180,797,450
Share-based compensation   (note 9)		535,533		556,640		—			—			1,092,173
Net loss for the period		—		—		(915,020	)		—			(915,020	)
Other comprehensive income		—		—		—			1,346,011			1,346,011
Balance, December 31, 2015	$	185,070,086	$	37,772,419	$	(62,186,634	)	$	21,664,743		$	182,320,614
Balance, September 30, 2016	$	210,756,585	$	39,146,155	$	(70,730,658	)	$	18,594,359		$	197,766,441
Share-based compensation   (note 9)		—		859,702		—			—			859,702
Net loss for the period		—		—		(6,317,410	)		—			(6,317,410	)
Other comprehensive loss		—		—		—			(4,402,428	)		(4,402,428	)
Balance, December 31, 2016	$	210,756,585	$	40,005,857	$	(77,048,068	)	$	14,191,931		$	187,906,305

The accompanying notes are an integral part of these unaudited condensed consolidated interim financial statements

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

1. Presentation of Financial Statements

Nature of Business

Merus Labs International Inc., incorporated under the Business Corporations Act (British Columbia), and its subsidiaries (the “Company”), operate in Canada and Europe. The registered and head office of the Company is 100 Wellington St. West, Ste. 2110, Toronto, Ontario M5K 1H1. The Company is a specialty pharmaceutical company engaged in the acquisition and licensing of branded prescription pharmaceutical products.

Basis of Preparation

These unaudited condensed consolidated interim financial statements (“interim financial statements”) of the Company have been prepared on a historical cost basis, except for certain financial assets which are presented at fair value, in accordance with International Financial Reporting Standards as issued by the International Accounting Standards Board (“IASB”) (“IFRS”) for interim financial statements. The interim financial statements have been prepared on a basis consistent with the Company’s annual audited consolidated financial statements for the year ended September 30, 2016. The interim financial statements are in compliance with International Accounting Standard 34, Interim Financial Reporting (“IAS 34”). Accordingly, certain information and note disclosure normally included in annual financial statements prepared in accordance with IFRS, have been omitted or condensed. During the quarter ended December 31, 2016, there were no significant changes in accounting policies or their application.

The preparation of the Company’s interim financial statements requires management to make judgments, estimates and assumptions that affect the reported amounts of revenues, expenses, assets and liabilities, and the disclosure of contingent liabilities, at the end of the reporting period. However, uncertainty about these assumptions and estimates could result in outcomes that require a material adjustment to the carrying amount of the asset or liability affected in future periods. The areas involving a higher degree of judgment or complexity, or areas where assumptions and estimates are significant to the financial statements have been set out in note 2 of the Company’s annual audited consolidated financial statements for the year ended September 30, 2016. These interim financial statements should be read in conjunction with the Company’s annual audited consolidated financial statements for the year ended September 30, 2016.

These interim financial statements were authorized for issue by the Company’s Board of Directors on February 13, 2017.

2. Acquisitions

Surgestone, Provames, Speciafoldine and Tredemine

On March 7, 2016, the Company acquired the rights to manufacture, market and sell Surgestone®, Provames®, Speciafoldine®, and Tredemine® pharmaceutical products (“Sanofi Portfolio”) in France from Sanofi S.A. (“Sanofi”) for a purchase price of €22,500,000 plus inventory on hand at closing. Surgestone® and Provames® are used in a variety of women's health indications, Speciafoldine® is used to treat macrocytic anemia and Tredemine® is a World Health Organization recognized essential medicine to treat tapeworm.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

The acquisition of the Sanofi Products pursuant to the Sanofi Purchase Agreement was funded by (i) the proceeds of the special warrants (note 9), together with (ii) an additional advance under the Company’s credit facility (note 7).

The acquisition was determined to be a business combination under IFRS 3 with the Company as the acquirer and the Sanofi Portfolio as the acquiree. Accordingly, the purchase price calculations and the purchase price allocations are dependent upon fair value estimates and assumptions as at the acquisition date.

Costs incurred to complete the acquisition were approximately $1,885,000, which were expensed during the period. The fair value of the acquired identifiable net assets was $33,639,383 (€22,984,000). The purchase price allocation to the following identifiable assets is based on their estimated fair values:

Inventory	$	1,646,550
Product rights - Surgestone		18,293,536
Product rights - Provames		1,369,930
Product rights - Speciafoldine		11,585,858
Product rights - Tredemine		743,509
Net assets acquired	$	33,639,383

Elantan, Isoket, and Deponit

On February 4, 2016, the Company completed the acquisition from UCB Pharma GmbH (“UCB”) of the nitrates business of UCB comprised of the rights to the Elantan®, Isoket® and Deponit® pharmaceutical products (the "Nitrates Portfolio") in Europe and select other markets. The Nitrates Portfolio were purchased pursuant to a purchase agreement entered into among the Company and one of its wholly owned subsidiaries.

The Nitrates Portfolio acquired include a variety of formats, including tablet, spray, patch and injectable presentations. The Nitrates Portfolio belong to a category of pharmaceuticals called nitrates, and are used to treat both acute and chronic coronary artery disease.

The Company acquired the exclusive rights to manufacture, market and sell the products in twenty European countries, Mexico, Turkey and South Korea. The European countries include France, Germany, Italy, Spain and the United Kingdom.

The UCB Products acquisition was structured as an all cash transaction pursuant to which the Company’s wholly owned subsidiary paid a purchase price of €92,000,000 on closing. In addition, the Company has agreed to purchase existing UCB Product inventory subsequent to the closing date. The Company funded the acquisition with a combination of cash-on-hand and proceeds from a new Euro-denominated debt facility (see note 7).

The acquisition was determined to be a business combination under IFRS 3 with the Company as the acquirer and the Nitrates Portfolio as the acquiree. Accordingly, the purchase price calculations and the purchase price allocations are dependent upon fair value estimates and assumptions as at the acquisition date.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

Costs incurred to complete the acquisition were approximately $532,000, which were expensed during the period. The fair value of the acquired identifiable net assets was $141,413,200 (€92,000,000). The purchase price allocation to the following identifiable assets is based on their estimated fair values:

Product rights - Elantan	$	73,073,734
Product rights - Isoket		38,458,242
Product rights - Deponit		29,881,224
Net assets acquired	$	141,413,200

3. Property and equipment

Continuity of property and equipment as at December 31, 2016 was as follows:

	Computer Equipment			Leasehold Improvements		Furniture and Fixtures			Manufacturing Equipment			Total
Cost at September 30, 2016	$	48,922		$	122,917	$	67,519		$	125,775		$	365,133
Additions		3,408			—		—			—			3,408
Foreign exchange differences		(104	)		—		(73	)		(4,881	)		(5,058	)
Cost at December 31, 2016	$	52,226		$	122,917	$	67,446		$	120,894		$	363,483
Accumulated Depreciation at September 30, 2016	$	6,404		$	5,122	$	5,967		$	25,155		$	42,648
Depreciation charge		3,699			3,073		3,327			3,067			13,166
Foreign exchange differences		(105	)		—		(28	)		(1,022	)		(1,155	)
Accumulated Depreciation at December 31, 2016	$	9,998		$	8,195	$	9,266		$	27,200		$	54,659
Carrying amount at September 30, 2016	$	42,518		$	117,795	$	61,552		$	100,620		$	322,485
Carrying amount at December 31, 2016	$	42,228		$	114,722	$	58,180		$	93,694		$	308,824

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

4. Intangible assets

Continuity of intangible assets as at December 31, 2016 was as follows:

	Product Rights			Patents			Computer Software			Total
Cost at September 30, 2016	$	409,499,967		$	22,874,352		$	501,402		$	432,875,721
Additions arising from internal development		172,915			—			68,479			241,394
Foreign exchange differences		(15,133,377	)		(887,601	)		(4,576	)		(16,025,554	)
Cost at December 31, 2016	$	394,539,505		$	21,986,751		$	565,305		$	417,091,561
Accumulated Amortization at September 30, 2016	$	81,177,881		$	21,451,948		$	—		$	102,629,829
Amortization charge		7,677,080			1,249,765			14,747			8,941,592
Foreign exchange differences		(2,562,976	)		(850,990	)		—			(3,413,966	)
Accumulated amortization at December 31, 2016	$	86,291,985		$	21,850,723		$	14,747		$	108,157,455
Carrying amount at September 30, 2016	$	328,322,086		$	1,422,404		$	501,402		$	330,245,892
Carrying amount at December 31, 2016	$	308,247,520		$	136,028		$	550,558		$	308,934,106

During the three months ended December 31, 2016, Management reviewed the amortization period and method applied to the Company’s product rights. It was determined that the amortization method previously being applied (straight-line) was not reflective of these assets’ economic benefit and rather the declining balance method of amortization is considered more appropriate. Further, the amortization period for certain product rights was revised to better reflect Management’s best estimate of the remaining useful life of these assets as of the beginning of the fiscal year. As a result of these changes in estimates, the amortization expense for the three months ended December 31, 2016 was approximately $1,300,000 lower than what would have been recorded under the previous method and period of amortization.

Certain computer software is not yet available for use and accordingly amortization has not yet commenced.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

5. Derivative liabilities

	December 31 2016		September 30 2016
Interest rate swap	$	669,877	$	837,584
Total derivative liabilities	$	669,877	$	837,584

In accordance with the terms of the Company’s long-term debt (note 7), during the third quarter of fiscal 2016 the Company entered into an interest rate swap for approximately 50% of the outstanding balance (€47,600,000 notional principal value at December 31, 2016), effectively fixing the maximum rate on that portion of the loan at 4.99% until maturity.

During the second quarter of fiscal 2015 the Company had entered into an interest rate swap for 50% of the outstanding balance of the previous senior secured facility, effectively fixing the rate on that portion of the loan at 5.72% until maturity. On January 22, 2016, the Company terminated the old interest rate swap contract resulting in a payment of $296,100, which represented the fair value of the liability on the settlement date.

6. Provisions

	Three months ended December 31, 2016			Year ended September 30, 2016
Balance at beginning of year	$	257,357		$	167,656
Charges		57,036			497,760
Utilization		(65,835	)		(407,150	)
Foreign exchange		(3,004	)		(909	)
Balance at end of year	$	245,554		$	257,357
Less: current portion of provisions		122,777			128,678
Non-current portion of provisions	$	122,777		$	128,679

The Company’s provisions are comprised of the following product-related liabilities:

Product Returns Liability:

The Company accepts all product returns relating to North American and certain European product sales. Management estimates the fair value of the product returns liability by taking into consideration the amount of units previously sold, returns experience to date, expiry of product currently in inventory, forecast sales volumes, and changes in the marketplace.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

7. Current and long-term debt

	December 31 2016		September 30 2016
Current
Operating line	$	9,000,000	$	5,000,000
Senior secured facility, €22,331,692 net of unamortized transaction costs of $1,190,655		30,451,119		36,070,095
Total current portion of debt	$	39,451,119	$	41,070,095

Non-Current
Senior secured facility, €72,577,996 net of unamortized transaction costs of $1,806,107	$	101,029,656	$	108,994,126
Total current and long-term debt	$	140,480,775	$	150,064,221

Euro Facility Amendment

On December 30, 2016, the Company amended its Euro Facility credit agreement (as defined below) to temporarily provide for increased working capital. The senior secured revolving credit facility was increased to $15,000,000 temporarily to the end of December 31, 2017, thereafter returning back to its original principal amount of $10,000,000. As a result certain covenants had to be adapted to account for this temporary increase. In addition, the cash flow sweep feature (discussed below) that had originally been contemplated to be calculated for the fiscal year ended September 30, 2016 was deferred to the fiscal year ended September 30, 2017. No changes were made to the amortization period or interest rate schedule of the original Euro Facility.

The amendment was determined to be a modification of the existing Euro Facility and therefore finance costs associated with the amendment of $409,974 were capitalized to the loan balance and will be amortized over the remaining term of the loan using the effective interest rate method.

Euro Facility

On February 1, 2016, in connection with the acquisition of the Nitrates Portfolio and Sanofi Portfolio, the Company refinanced its existing senior secured debt facility with a new Euro-denominated facility (“Euro Facility”). The Euro Facility was advanced under an amendment and restatement to the Company's existing credit agreement. Pursuant to the terms of the amended credit agreement, the lenders agreed to provide senior secured credit facilities in the aggregate amount of $180,000,000, comprising of a senior secured revolving credit facility in the principal amount of $10,000,000 and senior secured term facilities in the aggregate principal amount of $170,000,000, which were committed in Euros upon closing of the facility at a EUR:CAD exchange rate of 1.5225.

The proceeds from the senior secured term facility were used as follows: 1) €39,408,867 ($60,000,000) was used to refinance the Old Debt Facility (see below) on close; 2) €65,681,445 ($100,000,000) was used towards the acquisition of the Nitrates Portfolio on February 4, 2016; and 3) €6,568,144 ($10,000,000) was used towards the acquisition of the Sanofi Portfolio on March 7, 2016. In addition, $6,575,609 was drawn from the senior secured revolving credit facility upon closing of the Nitrates Portfolio acquisition on February 4, 2016, which was partially repaid prior to the year end.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

The senior secured term facility has a five year term at an initial coupon rate of EURIBOR (0% floor) plus 4.5% per annum, decreasing as the Company de-leverages, and quarterly principal repayments starting with June 30, 2016. As at December 31, 2016, the rate is EURIBOR (0% floor) plus 4.5%. The senior secured revolving credit facilities are due on demand and have an interest rate of Prime Rate plus 3.0% per annum, decreasing as the Company de-leverages.

Finance costs of $3,955,344 were capitalized to the loan balance and will be amortized over the term of the loan using the effective interest rate method. The unamortized portion of finance costs relating to the Old Debt Facility of $1,096,102 were written off during the prior fiscal year as the refinancing of the Old Debt Facility was determined to be an extinguishment of debt. The effective interest rate on the senior secured term facility at December 31, 2016 is 5.5%.

The senior secured term facility has an annual cash flow sweep feature, whereby 120 days after the fiscal year-end, commencing September 30, 2017 (as amended per above), the lender is entitled to 50% of excess cash flow as defined in the credit agreement. As at December 31, 2016, the Company has not included an estimate of the cash flow sweep entitlement amount pertaining to the current fiscal year end under the current portion of long-term debt as this amount would not be due until January 2018.

In accordance with the terms of the Euro Facility, during the third quarter of fiscal 2016, the Company entered into an interest rate swap for approximately 50% of the outstanding balance, effectively fixing the maximum rate on that portion of the loan at 4.99% until maturity.

All of the Company's obligations under the amended facility are guaranteed by all material subsidiaries of the Company and are secured by the material assets of the Company and the assets of, and all equity interests in its material subsidiaries. The Euro Facility contains affirmative and negative covenants including compliance with laws and restrictions on additional debt, as well as financial covenants such as debt to EBITDA and fixed charge coverage ratios. The Company was in compliance with all covenants of the senior secured credit facility during the year and at December 31, 2016.

Old Debt Facility

On September 5, 2014, the Company entered into a renegotiated secured debt facility (“Old Debt Facility”) with a syndicate of Canadian lenders. The Old Debt Facility provided additional funds for the purchase of Sintrom and refinanced the Company's then-existing senior secured debt at a lower rate and extended term. The facility matures on September 5, 2019 and provided for an $80,000,000 term loan at the Canadian BA rate plus 4.5%, or 5.3% effective rate, with principal repayments of $4,000,000 per quarter and monthly interest payments. Finance costs of $1,986,786 were capitalized to the loan balance and were amortized over the term of the loan.

In accordance with the terms of the Old Debt Facility, during the second quarter of fiscal 2015, the Company entered into an interest rate swap for 50% of the outstanding balance, effectively fixing the rate on that portion of the loan at 5.72% until maturity. The swap was unwound prior to the commencement of the new Euro Facility and all costs relating the unwinding were expensed in fiscal 2016.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

8. Preferred shares

On July 11, 2014, the Company completed a private placement subscription agreement to issue $10,000,000 of Series A convertible preferred shares (the “Series A Preferred Shares”) to a large Canadian institutional investor.

The Series A Preferred Shares pay a dividend of 8% per annum, subject to adjustment if the Company does not redeem after October 31, 2019. After October 31, 2019 the dividend rate is set to increase to LIBOR plus 10% for one year. Thereafter, the dividend rate will increase to LIBOR plus 12% into perpetuity. At any time at the option of the holder, the Series A Preferred Shares may be converted into the Company’s common shares at a conversion price of $2.20 per share. The Series A Preferred Shares are redeemable at the option of the Company at any time after October 31, 2019. The Series A Preferred Shares are also redeemable by the Company at any time in the event of a change of control subject to payment of a change of control premium. Costs associated with this transaction were approximately $52,000.

Based on management’s assessment of the various components of the Preferred Shares it was determined that the entire instrument should be recorded as a liability. Accordingly, dividends of $193,973 for the year ended December 31, 2016 (2015: $208,219) paid on the Preferred Shares are included in the finance costs in the statements of operations.

9.       Share capital

(a) Authorized:

Unlimited common shares without par value.

Issued:

	Three months ended December 31, 2016				Year ended September 30, 2016
	Number of shares		Amount		Number of shares		Amount
Balance, beginning of period		116,999,906	$	210,756,585		102,301,641	$	184,534,553
Common shares issued pursuant to prospectus offerings (b)		–		–		14,250,000		25,289,411
Common shares issued pursuant to performance share units (c)		–		–		298,265		535,533
Common shares issued pursuant to options exercise (d)		–		–		150,000		397,088
Balance, end of period		116,999,906	$	210,756,585		116,999,906	$	210,756,585

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

(b) Special warrants

On March 1, 2016, the Company completed, on a private placement basis, an offering of 14,250,000 subscription receipts of the Company (the “Subscription Receipts”), at a price of $1.90 per Subscription Receipt, for aggregate gross proceeds of $27,075,000 (the “Offering”). The proceeds of the Subscription Receipts were held in escrow and released to the Company upon the completion of the Sanofi French Products acquisition.  Upon closing of the acquisition, each Subscription Receipt was converted into one special warrant of the Company (the “Special Warrants”), with each Special Warrant being convertible into one common share of the Company. On May 18, 2016, the Special Warrants were converted into common shares under the Company's existing Base Shelf Prospectus, resulting in the issuance of 14,250,000 shares.

Transaction costs of $1,785,589 were incurred and have been capitalized against the proceeds from the Subscription Receipts.

On March 7, 2016, upon completion of the Sanofi French Products acquisition, the proceeds of the Offering, together with an advance under the Company’s amended and restated credit facility announced on February 1, 2016, were used to fund the acquisition.

(c) Performance Share Unit Plan

In January 2015, the Board approved the Performance Share Unit Plan (the “Plan”), which was approved by the Company’s shareholders on March 26, 2015. The Plan grants Performance Share Units to certain senior executives of the organization. The purpose of the plan is to provide the Company with greater flexibility with respect to equity compensation arrangements.

During the three months ended December 31, 2016, a total of 212,500 Units were issued to several executives as part of their ongoing compensation. Share based compensation expense in the amount of $282,968 was recognized for the three months ended December 31, 2016 (2015: $188,328), respectively, in connection with these and past grants.

On December 16, 2016, the Company determined that performance conditions with respect to fiscal 2016 metrics had been met and, as such, authorized the issuance of a total of 345,242 shares (2015: 298,265 shares) pursuant to the grants in satisfaction of those amounts earned under the Performance Share Unit plan. These shares were issued subsequent to December 31, 2016 and are therefore considered issuable shares at December 31, 2016.

(d) Stock option plan

The Company has reserved 11,699,990 common shares under a 10% rolling reloading stock option plan. Under the plan, the options are exercisable for one common share and the exercise price of the option must equal the market price of the underlying share at the grant date. The options have vesting periods ranging from the date of grant up to three years. Once vested, options are exercisable at any time until expiry.

During the year ended December 31, 2016, the Company granted 1,715,000 options (2015: 1,755,000 options) to management, staff and directors, with exercise price $1.00 per share (2015: $1.71). The options have a term of five years and vest over a period of two years from the date of grant.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

The estimated fair value of the options granted during the three months ended December 31, 2016, using the Black-Scholes option pricing model, was $880,598 (2015: $1,703,754). $576,734 was expensed in the financial statements during the three months ended December 31, 2016 (2015: $903,845), respectively, relating to current and prior period grants and has been included in share-based compensation in the statements of operations and in equity as equity reserves. The remaining expense will be recognized over the balance of the vesting periods.

(e) Stock option details

The fair value of each option granted was estimated on the date of the grant using the Black-Scholes fair value option pricing model with the following assumptions:

	Three months ended December 31
	2016		2015
Weighted-average fair value of options		$ 0.51	$ 0.97
Risk-free interest rate		0.92%	0.80%
Volatility of the Company's common shares		65%	69%
Weighted average expected life of the options		5 years	5 years
Forfeiture rate		8.70%	8.70%
Expected dividends		Nil	Nil

Volatility was determined based on daily observations of the historical stock price over a period consistent with the expected life of the options at the date of grant.

Details of the options are as follows:

	Number of		Weighted average
	options		price per option
	outstanding		outstanding
Options outstanding, September 30, 2015	3,818,500		$	1.86
Options granted	2,015,000			1.70
Options expired	(525,000	)		1.95
Options exercised	(150,000	)		1.66
Options outstanding, September 30, 2016	5,158,500		$	1.79
Options granted	1,715,000			1.00
Options outstanding, December 31, 2016	6,873,500		$	1.60

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

The range of exercise prices for outstanding and exercisable options at December 31, 2016 are as follows:

Exercise Price	Number Outstanding	Weighted Average Contractual Life	Number Exercisable	Weighted Average Exercisable Strike Price
$0.50 - $1.00	1,873,500	4.67	730,165	$0.99
$1.01 - $1.50	50,000	0.62	50,000	$1.19
$1.51 - $2.00	4,375,000	3.10	3,701,675	$1.74
$2.01 - $2.50	200,000	0.03	200,000	$2.02
$2.51 - $3.00	375,000	3.30	250,001	$2.81
$0.50 - $3.00	6,873,500	3.43	4,931,841	$1.78

10. Commitments and contingencies

(a) Operating lease commitments

The Company has entered into non-cancellable operating lease agreements for office premises and equipment with minimum annual lease payments to expiry as follows:

	December 31 2016		September 30 2016
Less than 1 year	$	300,540	$	300,540
1 to 2 years		300,540		300,540
2 to 3 years		300,540		300,540
3 to 4 years		300,540		300,540
Thereafter		100,180		175,315
Total	$	1,302,340	$	1,377,475

Lease expense recognized during the period ended December 31, 2016 was $166,879 (2015: $50,037), which has been included in general and administrative expenses in the consolidated statements of operations.

(b) Legal proceedings

Arbitration Proceeding

In August 2014, the Company received notice of a request for arbitration from LG Life Sciences (“LGLS”), the original owner of the Company’s former Factive® product. This request for arbitration was based on the original license agreement entered into by LGLS and Cornerstone Therapeutics, Inc. (now Chiesi USA, Inc.). The request for arbitration named the Company as a respondent together with Chiesi and Vansen Pharma, Inc. The request for arbitration included the allegation that Cornerstone did not have the legal right to transfer the Factive product to the Company. LGLS sought an award for damages relating to an alleged breach of contract, as well as disgorgement of revenue and other benefits derived by us from sales of Factive. The Company has successfully defended this claim. Additionally, the Company and Chiesi have each asserted claims against one another, seeking indemnity and damages related to LGLS’s claim. These claims along with any new liabilities in the form of the cost of damages incurred by LGLS resulting from Vansen’s failure to return the license to sell Factive to LGLS have also been resolved.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

The Company had contingent liabilities remaining at September 30, 2016 in the form of the Company’s indemnification of Cornerstone’s liability under the Factive asset purchase agreement, that included the cost of reimbursing wholesalers for expired goods on behalf of Cornerstone, the cost of paying for government reimbursement programs on behalf of Cornerstone, and legal costs incurred by Cornerstone to defend themselves against LGLS’s original claim. On December 18, 2016, the Company reached an out of court settlement in regards to all these claims in the amount of US$650,000, which has been included in general and administrative expense in the statement of operations for the three months ended December 31, 2016 along with unrecoverable deposits previously paid for the arbitration proceedings in the amount of $125,458. This amount was paid subsequent to December 31, 2016.

 

(c) Revenue based commitments

Pursuant to the Company’s exclusive license agreement with EISAI, the Company is subject to a royalty fee of 20% based on the net sales of Salagen.

Pursuant to the Company’s technology transfer and manufacturing agreement with a contract manufacturer, the Company is subject to a royalty fee based on the capsule volume of Vancocin sold.

(d) Purchase commitments

Pursuant to the Company’s raw materials supply agreement with a contract manufacturer, the Company is committed to purchasing approximately $2,500,000 of product per calendar year from 2017 to 2023.

11. Related party transactions

At December 31, 2016 and September 30, 2016, there were no amounts owing to or from related parties. The remuneration of directors and other members of key management personnel recorded in the general and administrative line of operating expenses are as follows: 

		Three months ended December 31
		2016		2015
Salaries	$	480,449	$	501,147
Share based compensation		788,022		1,092,173
	$	1,268,471	$	1,593,320

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

12. Finance costs

Finance costs for the three months ended December 31, 2016 and 2015 are comprised of:

	Three months ended December 31
	2016		2015
Interest expense	$	1,723,415	$	802,528
Amortization of transaction costs		485,147		145,101
Total	$	2,208,562	$	947,629

13. Income taxes

The major components of income tax (recovery) expense for the three months ended December 31, 2016 and 2015 are:

	Three months ended December 31
Income tax recognized in profit or loss	2016		2015
Current tax
Current period tax expense	$	475,009	$	131,561
Provision for income taxes	$	475,009	$	131,561

14. Management of capital

The Company includes the following in its definition of capital:

December 31                    September 30
	2016			2016
Debt comprised of:
Senior secured facility	$	140,480,775		$	150,064,221
Preferred shares		9,947,730			9,947,730
Equity comprised of:
Share capital		210,756,585			210,756,585
Equity reserve		40,005,857			39,146,155
Deficit and AOCI		(62,856,137	)		(52,136,299	)
	$	338,334,810		$	357,778,392

The Company’s objectives when managing capital are:

(a) to allow the Company to respond to changes in economic and/or marketplace conditions;

(b) to give shareholders sustained growth in shareholder value by increasing shareholders’ equity;

(c) to ensure that the Company maintains the level of capital necessary to meet the requirements of its long-term debt;

(d) to comply with financial covenants required under its debt facilities; and

(e) to maintain a flexible capital structure which optimizes the cost of capital at acceptable levels of risk

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

The Company manages its capital structure and makes adjustments to it in light of changes in economic conditions and the risk characteristics of its underlying assets. The Company maintains or adjusts its capital level to enable it to meet its objectives by:

(a) raising capital through equity financings;

(b) utilizing leverage in the form of third party debt; and

(c) realizing proceeds from the disposition of its investments

The Company is not subject to any capital requirements imposed by a regulator. The Company is subject to certain capital requirements and negative covenants with respect to its Senior Secured Facility (refer to note 7). There were no changes in the Company’s approach to capital management during the period. To date, the Company has not declared any cash dividends to its common shareholders as part of its capital management program. The Company’s management is responsible for the management of capital and monitors the Company’s use of various forms of leverage on a regular basis.

15. Financial instruments and financial risk management

a) Fair Value Estimation

The Company’s carrying value of cash and cash equivalents, short-term investments, trade and other receivables, and accounts payable and accrued liabilities approximate their fair values due to the immediate or short term maturity of these instruments. The fair value of other financial liabilities such as the Company’ s operating line, long term debt, and preferred shares is not materially different than its carrying value due to the recent issuance of these liabilities.

Carrying value and fair value of financial assets and liabilities are summarized as follows:

December 31, 2016
Classification	Carrying value		Fair value
Financial assets at FVTPL		$		$
- Short-term investments		3,210		3,210
Loans and receivables
- Cash and cash equivalents		3,979,691		3,979,691
- Trade and other receivables		31,315,927		31,315,927
Other financial liabilities
- Accounts payable and accrued liabilities		20,508,667		20,508,667
- Operating line		9,000,000		9,000,000
- Long term debt		131,480,775		134,477,537
- Preferred shares		9,947,730		10,000,000
Financial liabilities at FVTPL
- Derivative liabilities		669,877		669,877

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

September 30, 2016
Classification	Carrying value		Fair value
Financial assets at FVTPL		$		$
- Short-term investments		3,155		3,155
Loans and receivables
- Cash and cash equivalents		3,213,564		3,213,564
- Trade and other receivables		28,597,219		28,597,219
Other financial liabilities
- Accounts payable and accrued liabilities		15,875,494		15,875,494
- Operating line		5,000,000		5,000,000
- Long term debt		145,064,221		148,136,156
- Preferred shares		9,947,730		10,000,000
Financial liabilities at FVTPL
- Derivative liabilities		837,584		837,584

The Company is required to present information about its financial assets and liabilities with respect to the hierarchy of the valuation techniques the Company utilized to determine fair value. The different levels have been defined as follows:

• Level 1 inputs utilize quoted prices (unadjusted) in active markets for identical assets or liabilities

• Level 2 inputs utilize data points that are observable such as quoted prices, interest rates and yield curves

• Level 3 inputs are unobservable data points for the asset or liability, and includes situations where there is little, if any, market activity for the asset or liability.

At December 31, 2016, the Company’s financial assets and liabilities would be classified as follows:

				Significant		Significant Other		Significant
				Observable		Observable		Unobservable
				Inputs		Inputs		Inputs
	December 31, 2016			(Level 1)		(Level 2)		(Level 3)
Assets:
Short-term investments	$	3,210	$	3,210	$	–	$	–
	$	3,210	$	3,210	$	–	$	–
Liabilities:
Derivative liabilities	$	669,877	$	–	$	669,877	$	–
	$	669,877	$	–	$	669,877	$	–

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

At September 30, 2016, the Company’s financial assets and liabilities would be classified as follows:

				Significant		Significant Other		Significant
				Observable		Observable		Unobservable
				Inputs		Inputs		Inputs
	December 31, 2016			(Level 1)		(Level 2)		(Level 3)
Assets:
Short-term investments	$	3,155	$	3,155	$	–	$	–
	$	3,155	$	3,155	$	–	$	–
Liabilities:
Derivative liabilities	$	837,584	$	–	$	837,584	$	–
	$	837,584	$	–	$	837,584	$	–

The fair value of financial instruments traded in active markets is based on quoted market prices at the statement of financial position date. A market is regarded as active if quoted prices are readily and regularly available from an exchange, dealer, broker, industry group, pricing service, or regulatory agency, and those prices represent actual and regularly occurring market transactions on an arm’s length basis.

The fair value of financial instruments that are not traded in an active market (for example, over-the-counter derivatives) is determined by using valuation techniques. These valuation techniques maximize the use of observable market data where it is available and rely as little as possible on entity specific estimates. If all significant inputs required to fair value an instrument are observable, the instrument is included in Level 2.

If one or more significant inputs are not based on observable market data, the instrument is included in Level 3.

b) Financial Risk Factors

The use of financial instruments can expose the Company to several risks, including market, credit and liquidity risks. Apart from the risks listed below, management is of the opinion that they are not exposed to any other significant risks. A discussion of the Company’s use of financial instruments and its risk management is provided below.

(i) Liquidity risk

Liquidity risk is the risk that the Company will not have sufficient cash resources to meet its financial obligations as they come due. The Company’s liquidity and operating results may be adversely affected if the Company’s access to the capital markets is hindered, whether as a result of a downturn in stock market conditions generally or related to matters specific to the Company. In order to mitigate this risk, the Company maintains a sufficient cash balance in order to satisfy short-term liabilities as they come due and actively pursues raising capital through various public and private financing mechanisms to satisfy longer term needs.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

The table below analyzes the Company’s non-derivative financial liabilities into relevant maturity groupings based on the remaining period at the statement of financial position date to the contractual maturity date. The amounts disclosed in the table are the contractual undiscounted cash flows and do not include capitalized transaction costs.

	Years ended September 30
At December 31, 2016	2017		2018		2019		Thereafter
Operating line	$	9,000,000	$	–	$	–	$	–
Senior Secured Facility		23,731,331		31,641,774		31,641,774		47,462,659
Accounts payable and       accrued liabilities		20,508,667		–		–		–
Income taxes payable		1,083,098		–		–		–
Total	$	54,323,096	$	31,641,774	$	31,641,774	$	47,462,659

	Years ended September 30
At September 30, 2016	2016		2017		2018		Thereafter
Operating line	$	5,000,000	$	–	$	–	$	–
Senior Secured Facility		37,266,232		32,919,147		32,919,147		45,031,630
Accounts payable and       accrued liabilities		15,875,494		–		–		–
Income taxes payable		635,891		–		–		–
Total	$	58,777,617	$	32,919,147	$	32,919,147	$	45,031,630

(ii) Market risk:

Market risk is the risk that the fair value of, or future cash flows from, the Company’s financial instruments will significantly fluctuate because of changes in market prices. The value of the financial instruments can be affected by changes in interest rates, foreign exchange rates, and equity and commodity prices. The Company is not exposed to significant market risk given the low value of its investments.

(iii) Currency risk:

The Company is subject to currency risk through its sales of products and services denominated in foreign currencies (primarily Euros), purchases of inventory in Euros and US dollars and product acquisitions denominated in foreign currencies. As such, changes in the exchange rate affect the operating results of the Company. Dependent on the nature, amount and timing of foreign currency receipts and payments, the Company may from time to time enter into foreign currency derivative contracts to reduce its exposure to foreign currency risk. The Company’s Euro Facility also provides a natural hedge against its Euro sourced revenues, thus minimizing the need for foreign currency derivative contracts.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

The following significant monetary financial assets and liabilities were denominated in foreign currencies at December 31, 2016 (U.S. dollar 1.3427, Euro 1.4169, British pound 1.6565, Swiss franc 1.3214) and September 30, 2016 (U.S. dollar 1.3117, Euro 1.4741, British pound 1.7069, Swiss franc 1.3531):

	December 31 2016			September 30 2016
Canadian Dollar Equivalent :
Denominated in US dollars	$	(1,300,837	)	$	(1,631,182	)
Denominated in Euros		(127,946,875	)		(143,423,582	)
Denominated in British pounds		4,925,894			5,121,046
Denominated in Swiss francs		1,451,323			431,128
Net (liabilities) assets denominated in foreign currencies	$	(125,773,141	)	$	(139,502,589	)

The Company has a Euro denominated debt facility (included in the table above), which serves as a natural hedge against the Company’s Euro-denominated investments in its European subsidiaries that are in the form of intercompany loans, which are eliminated upon consolidation.

The following table shows the estimated sensitivity of the Company’s total comprehensive gain (loss) for the period ended December 31, 2016 from a change in foreign currencies with all other variables held constant as at December 31, 2016:

		Change in net after-tax			Change in net after-tax
Percentage change in		gain from % increase			loss from % decrease
foreign currencies		in foreign currencies			in foreign currencies
2%	$	(2,515,463.00	)	$	2,515,463
4%		(5,030,926.00	)		5,030,926
6%		(7,546,388.00	)		7,546,388
8%		(10,061,851.00	)		10,061,851
10%		(12,577,314.00	)		12,577,314

(iv) Credit risk:

Some of the Company’s financial assets, including cash and cash equivalents and short-term investments are exposed to the risk of financial loss occurring as a result of default of a counterparty on its obligations to the Company. The Company may, from time to time, invest in debt obligations. The Company is also exposed, in the normal course of business, to credit risk from customer receivables. These amounts are continually monitored by management for collectability, and, in general, are lower risk as they are typically due from large institutions or multinational distributors.

(v) Interest rate risk:

Merus has significant current and long-term debt in the form of senior secured debt which currently bears interest at a floating interest rate of EURIBOR (0% floor) plus 4.5% and will incur greater interest expenses if the EURIBOR rate rises. Management has reduced this risk by entering into an interest rate swap arrangement as allowed for through facilities in its credit agreement. Interest rate swaps effectively fix the interest rate on the debt to which they are applied. At December 31, 2016, Merus had interest rate swaps applied to approximately 50% of its senior secured debt facility.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

16. Segment information

The Company operates in a single reportable segment focused on acquiring, in-licensing, marketing and distributing pharmaceutical products in Canada and internationally. The Company carries out business principally in Canada and Europe.

Revenues by geographic region are detailed as follows:

	Three months ended December 31
	2016		2015
Canada	$	1,155,822	$	1,864,374
International		24,912,982		14,061,477
	$	26,068,804	$	15,925,851

Other than Canada, the Company derived more than 10% of its revenues in the three months ended December 31, 2016 or three months ended December 31, 2015 period from France, Germany, the Netherlands, and Spain. Revenues in France of $3,255,976 (2015: $570,210), Germany of $3,532,083 (2015: $3,806,346), the Netherlands of $2,895,645 (2015: nil), and Spain of $4,558,958 (2015: $3,838,253), and are included in International in the table above.

Long-term assets by geographic region are comprised of product rights and patents and property and equipment, detailed as follows:

	December 31		September 30
	2016		2016
Canada	$	2,187,193	$	2,177,950
International		307,055,737		328,390,427
	$	309,242,930	$	330,568,377

17. Prior period reclassification

Cost of goods sold and Selling and marketing expenses

The line item cost of goods sold in the Company’s statements of operations has historically included any costs directly attributable to the products sold, which is mainly comprised of the carrying cost of goods sold, inventory write-downs or reversals, royalties payable on current sales, and certain manufacturer pass-through expenses (e.g. stability testing). The operating expense line item selling and marketing in the Company’s statements of operations has included all activities related to supporting the sales of its products, which includes distribution, marketing, promotion, quality control, and regulatory support.

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

Based on Management’s internal approach for analysing the Company’s financial performance as well as feedback from the readers of the financial statements, Management has determined that the relevance, reliability, and comparability of the Company’s consolidated financial statements can be improved by reclassifying all costs directly related to the logistics, warehousing, release, and distribution of the Company’s products from selling and marketing expenses and general and administrative to cost of goods sold. There has been no impact to net income or (loss) as a result of this reclassification.

Thus, certain amounts have been reclassified from general and administrative and selling and marketing to cost of goods sold in the prior year to conform to current year presentation.

Impact of Reclassification

The impact of the above reclassification adjustments have been summarized below. These reclassification adjustments have no impact on net income (loss) and therefore only the statements of operations is disclosed.

For the period ended     December 31, 2015		As previously reported		Adjustment			As restated
Statement of Operations:
Revenues	$	15,925,851		–		$	15,925,851
Cost of goods sold		4,484,811		137,176			4,621,987
Gross margin		11,441,040		137,176			11,303,864
Operating expenses:
Selling and marketing		1,392,556		(137,176	)		1,255,380
General and administrative		1,513,209		–			1,513,209
Share-based compensation		1,092,173		–			1,092,173
Amortization of intangible assets		7,356,701		–			7,356,701
Depreciation		3,854		–			3,854
Foreign exchange gains		(570,697	)	–			(570,697	)
		11,140,115		(137,176	)		11,002,939
Operating income		300,925		–			300,925
Finance costs		947,629		–			947,629
Derivative losses		136,872		–			136,872
Investment income		(117	)	–			(117	)
Loss before income taxes		(783,459	)	–			(783,459	)
Income tax expense - current		131,561		–			131,561
Net income for the year	$	(915,020	)	–		$	(915,020	)

Merus Labs International Inc.

Notes to the Condensed Consolidated Interim Financial Statements

(Unaudited)

(Expressed in Canadian dollars)

For the three months ended December 31, 2016 and 2015

18. Net Investment in Foreign Operation

For the year ended September 30, 2015 and prior, the Company recognized any foreign exchange gains and losses on its intercompany loans in other comprehensive income as it considered these amounts as part of its net investment in a foreign operation. These intercompany loans were started to be repaid in fiscal 2016 and as such the Company expects that going forward they will be settled. Accordingly, these loans no longer met the definition of a net investment in a foreign operation under IAS 21 during the year ended September 30, 2016. Thus, any foreign exchange gains and losses on these loans recorded during the year ended September 30, 2016 and beyond will be recorded through net income (loss). Any historical amounts ($9,822,703 accumulated gain) recorded will be recycled out of AOCI on the disposal of the foreign operations.