UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549

SCHEDULE 14A

Proxy Statement Pursuant to Section 14(a) of the Securities Exchange Act of 1934 (Amendment No. )

Filed by the Registrant x

Filed by a Party other than the Registrant o

Check the appropriate box:
o	Preliminary Proxy Statement
o	Confidential, for Use of the Commission Only (as permitted by Rule 14a-6(e)(2))
o	Definitive Proxy Statement
x	Definitive Additional Materials
o	Soliciting Material under §240.14a-12

Regeneron Pharmaceuticals, Inc.
(Name of Registrant as Specified In Its Charter)


(Name of Person(s) Filing Proxy Statement, if other than the Registrant)

Payment of Filing Fee (Check the appropriate box):
x	No fee required.
o	Fee computed on table below per Exchange Act Rules 14a-6(i)(1) and 0-11.
	(1)		Title of each class of securities to which transaction applies:

	(2)		Aggregate number of securities to which transaction applies:

	(3)		Per unit price or other underlying value of transaction computed pursuant to Exchange Act Rule 0-11 (set forth the amount on which the filing fee is calculated and state how it was determined):

	(4)		Proposed maximum aggregate value of transaction:

	(5)		Total fee paid:

o	Fee paid previously with preliminary materials.
o	Check box if any part of the fee is offset as provided by Exchange Act Rule 0-11(a)(2) and identify the filing for which the offsetting fee was paid previously. Identify the previous filing by registration statement number, or the Form or Schedule and the date of its filing.
	(1)	Amount Previously Paid:

	(2)	Form, Schedule or Registration Statement No.:

	(3)	Filing Party:

	(4)	Date Filed:

DE A R SH A REHOLDERS, 2015 was a busy and rewarding year for Regeneron as we made major strides in advancing our mission of bringing important new medicines to people with serious diseases, over and over again. This year, for the first time, our Annual Report integrates reporting on our citizenship priorities and aspirations, in addition to our financial and business We delivered EYLEA® (aflibercept) Injection, our therapy for serious vision-threatening diseases, to more and more patients, and we launched PRALUENT® (alirocumab) Injection, a first-in-class therapy for uncontrolled performance. LDL cholesterol in certain patients. We invite you to read about our 2015 accomplishments, financial performance and citizenship efforts below and in our 2015 Annual Report on Form 10-K, available on the Investor Relations portion of our website. In the next few years, we anticipate additional approvals for a number of new therapies. In 2016, we look forward to potentially launching sarilumab for rheumatoid arthritis, pending U.S. Food and Drug Administration (FDA) review of our application. We also expect a potential U.S. regulatory submission for dupilumab in atopic dermatitis, a serious form of eczema, for which we have been granted a Breakthrough Therapy designation by the FDA. Unfortunately, there was also some sadness in 2015. Our longtime friend, mentor, co-founder and Board member, Dr. Alfred G. Gilman, passed away in December. Dr. Gilman was a Nobel Laureate who made lasting contributions to science and medicine. On a personal level, we all benefited greatly from Al’s counsel and wry wit over the years, and we will miss him greatly. Our pipeline of a dozen clinical-stage antibodies continues to progress, with important programs in eye disease, cancer, infectious disease, pain, cardiovascular disease and inflammation. We also continue to invest in technology and innovation that will position us to bring needed new medicines to patients for many years into the future. Likewise, we have made important infrastructure investments to ensure our long-term success, including adding two new buildings at our headquarters in Tarrytown, New York, and expanding our Industrial Operations facilities in Rensselaer, New York, and Raheen, Ireland. We look forward to updating you on our progress as we continue building Regeneron into a leading global biopharmaceutical company. Sincerely, Leonard Schleifer, MD, PhD Roy Vagelos, MD We have always run Regeneron by the principle of “doing well by doing good.” In addition to our work to invent new and needed medicines, we focus on improving our world and operating with the highest standards of integrity. George Yancopoulos, MD, PhD 2 0 1 5 A N N UA L R E P O R T 4 < M E N U >

EYLEA® (AFLIBERCEPT) INJECTION AND RETINAL DISEASE PROGRAMS Market-leading VEGF-Trap approved in more than 100 countries for the treatment of many blindness-causing retinal conditions, including wet age-related macular degeneration and diabetic macular edema (DME). E Y L E A U.S . S A L ES : 5 4% INCRE A SE $2.676 bn EYLEA net sales in the U.S. increased 54% to $2.676 billion for the full year of 2015, from $1.736 billion for the full year 2014. Outside of the U.S., where our collaborator Bayer HealthCare commercializes EYLEA, net sales were $1.413 billion in 2015, compared to $1.039 billion in 2014. Regeneron recognized $467 million from its share of net profit outside the U.S. in 2015, compared to $ 301 million in 2014. This growth was driven in part by the publication in early 2015 of first-year results from an independent National Institutes of Health (NIH) -sponsored comparative effectiveness study in DME. In the study, at one year, EYLEA demonstrated a significantly greater improvement in mean change in best-corrected visual acuity (BCVA) from baseline compared to ranibizumab and bevacizumab, two other VEGF inhibitors used in retinal disease. The rates of most ocular and systemic adverse events were similar across the three study groups. E Y L E A E X-U.S . S A L ES : 36 % INCRE A SE $1.413 bn $1.736 bn $1.409 bn $1.039 bn In 2016, we initiated a Phase 3 study of EYLEA in diabetic retinopathy in patients without DME, a common degenerative eye disease that impacts people with diabetes. We continue to explore EYLEA in combination with other mechanisms, and have two ongoing clinical programs in this area, aflibercept+PDGFR-beta and aflibercept+ANG2, in collaboration with Bayer HealthCare. $427.1 mm 2 0 13 20 1 4 2 0 15 2 0 13 20 1 4 2 0 15 2 0 1 5 A N N UA L R E P O R T 6 < M E N U >

PR ALUEN T ® ( ALIROCUMAB) IN JEC T ION Only monoclonal antibody targeting PCSK9 (proprotein convertase subtilisin/kexin type 9) available in two doses, allowing for tailored therapy based on a patient’s LDL-C lowering needs. In July 2015, PRALUENT was approved by the FDA as adjunct to diet and maximally tolerated statin therapy for the treatment of adults with heterozygous familial hypercholesterolemia or clinical atherosclerotic cardiovascular disease, who require additional lowering of LDL-C (often referred to as “bad cholesterol”). The effect of PRALUENT on cardiovascular morbidity and mortality has not been determined. Together with our collaborator Sanofi, the U.S. launch is underway. We have focused on physician education about this new class, as well as achieving patient access and reimbursement coverage from health plans. PRALUENT was also approved in the E.U., and launches are underway across the region. The ongoing ODYSSEY OUTCOMES clinical trial program, which is evaluating the potential of PRALUENT to prevent heart attacks, stroke and cardiac death, reached full enrollment in 2015, with more than 18,000 patients at more than 2,000 study centers. Interim results are possible in late 2016, and we expect full results in 2017. ODY SSE Y OU T COMES 2 0 1 5 A N N UA L R E P O R T 7 < M E N U >

PIPELINE (as of April 2016) Regeneron has a dozen fully human monoclonal antibodies in clinical development, all of which were developed using our proprietary VelocImmune® technology. P H A S E 1 P H A S E 2 P H A S E3 REGN1979 CD20/CD3 Antibody Cancer DUPILUMAB* IL-4R Antibody Atopic dermatitis in children, nasal polyps, eosinophilic esophagitis EVINACUMAB Angptl3 Antibody Lipid disorders ALIROCUMAB* PCSK9 Antibody Cardiovascular outcomes REGN1908-1909 Allergic disease REGN910-3^ Nesvacumab (Ang2 Antibody) + Aflibercept Ophthalmology AFLIBERCEPT^ VEGF-Trap Diabetic retinopathy without DME SARILUMAB* IL-6R Antibody Non-infectious uveitis SARILUMAB* IL-6R Antibody Rheumatoid arthritis TREVOGRUMAB GDF8 Antibody Skeletal muscle disorders REGN2810* PD-1 Antibody Cancer DUPILUMAB* IL-4R Antibody Atopic dermatitis in adults, asthma FASINUMAB † NGF Antibody Chronic lower back pain REGN2176-3^ Rinucumab (PDGFR-beta Antibody) + Aflibercept Wet age-related macular degeneration REGN2222 RSV Antibody Respiratory syncytial virus FASINUMAB † NGF Antibody Pain due to osteoarthritis * in collaboration with Sanofi ^ in collaboration with Bayer HealthCare † in collaboration with Mitsubishi Tanabe 2 0 1 5 A N N UA L R E P O R T 9 < M E N U >

SARILUMAB An anti-IL-6 monoclonal antibody under U.S. regulatory review for the treatment of rheumatoid arthritis (RA). U N M E T N E E D IN R H E U M AT O ID A R T H R I T IS R E M A IN S In 2015, we reported positive data from three Phase 3 trials of sarilumab in patients with rheumatoid arthritis. Together with our collaborator, Sanofi, we submitted the U.S. Biologics License Application in November 2015 and were assigned a Prescription Drug User Fee Act (PDUFA) date of October 30, 2016. R A IMPA C T S MORE T H A N 1.3 MILLION A MERICA NS 1 In March 2016, the Phase 3 SARIL-RA-MONARCH monotherapy study met its primary endpoint by demonstrating that sarilumab was superior to adalimumab (Humira®) in improving signs and symptoms of active RA at Week 24. The incidence of adverse events, serious adverse events, infections and serious infections was generally similar between groups. — While significant strides have been made in the treatment of RA, there are continued unmet needs — A central driver of the destructive effects of RA in the joints is persistently elevated levels of IL-6, a signaling protein in the body.2-5 At normal levels, IL-6 is responsible for contributing to the healing process after injury or infection.3,6-7 However, at persistently raised levels, IL-6 triggers inflammation that can destroy bone and cartilage5,8-12 — IL-6 may also contribute to the multiple systemic effects of RA, including fatigue, anemia and bone density loss2 2 0 1 5 A N N UA L R E P O R T 10 < M E N U >

DUPILUM A B A first-in-class investigational monoclonal antibody blocking IL-4 and IL-13, two key cytokines believed to be drivers in allergic inflammation. AT O P I C D E R M AT I T IS : U N M E T N E E D IN A D E V A S TAT IN G A N D M I S U N D E R S T O O D D I S E A S E Dupilumab is being studied for the treatment of certain allergic conditions, including atopic dermatitis (AD), uncontrolled asthma, nasal polyps and eosinophilic esophagitis. A P P ROX IM AT ELY 1.6 MILLION U.S. A DULT S A RE E S T IM AT ED T O H AV E UNCON T ROL L ED MODERATE -T O - SE V ERE AT OP IC DERM AT I T IS 13 Dupilumab was granted a Breakthrough Therapy designation by the FDA for the treatment of adults with moderate-to-severe atopic dermatitis who are not adequately controlled with topical prescription therapy and/or for whom these treatments are not appropriate. We expect to submit an application for FDA approval later this year. In 2016, we reported positive topline results from two large Phase 3 studies in atopic dermatitis and continue to enroll patients in a second pivotal study in asthma. In the atopic dermatitis studies, the overall rate of adverse events was comparable between the dupilumab groups and the placebo groups. — Currently, only topical therapies have been approved by the FDA — Systemic immuno-suppressants are used off-label, but can have significant side effects 2 0 1 5 A N N UA L R E P O R T 11 < M E N U >

REGN2222 A fully human monoclonal antibody being investigated for the prevention of serious lower respiratory tract infections associated with Respiratory Syncytial Virus (RSV). FASINUM A B An antibody targeting nerve growth factor being evaluated for the potential to offer a novel, non-opioid approach to addressing chronic pain. Two clinical trials of fasinumab for pain due to osteoarthritis and chronic back pain were initiated in 2016. In 2015, we entered into a collaboration with Mitsubishi Tanabe Pharma Corporation to develop and commercialize fasinumab in Japan, Korea and nine other Asian countries (excluding China). In 2015, we initiated the Phase 3 NURSERY-Pre-term trial that will evaluate the efficacy, safety, pharmacokinetics and immunogenicity of REGN2222 in infants under the age of six months. U N M E T N E E D IN A V U LN E R A BLE PO P U L AT I O N 1 IN 5 INFA N T S UNDER 6 MON T HS W IL L RE QUIRE MEDIC A L AT T EN T ION F OR RS V14 U N M E T N E E D IN C H R O N I C P A I N A P P ROX IM AT ELY 50 MILLION U.S. A DULT S SUF F ER F ROM SIGNIF IC A N T CHRONIC OR SE V ERE PA IN 15 2 0 1 5 A N N UA L R E P O R T 12 < M E N U >

IMMUNO - ONCOLOGY R A PID RESPONSE + INFEC T IOUS DISE ASE Building on our existing Sanofi antibody collaboration, we launched a new $2.2B global immuno-oncology collaboration with Sanofi. Regeneron’s Rapid Response capabilities leverage our core VelociSuite® technologies to significantly compress the time required for discovery and preclinical validation of potential treatments for emerging infectious diseases. This new undertaking will provide important new resources to advance our portfolio in this rapidly developing field, which seeks to harness the body’s immune system to fight cancer. In 2015, we identified and validated a novel therapeutic cocktail of three antibodies targeting the Ebola virus, and reached an agreement with the Biomedical Advanced Research and Development Authority (BARDA) of the U.S. Department of Health and Human Services to develop, test and manufacture this potential treatment. A Phase 1 study in healthy volunteers is planned for the first half of 2016. We similarly identified and validated an antibody against MERS (Middle East Respiratory Virus) and are working to advance this program, as well as pursuing antibody therapies for other devastating viral diseases such as Zika and Dengue. We continued to explore multiple approaches in immuno-oncology, including bispecific antibodies, checkpoint inhibitors and antibody drug conjugates. We have two antibodies, a CD20/CD3 bispecific antibody and a PD-1 inhibitor, in clinical studies with data expected in 2016. A number of additional immuno-oncology antibodies are expected to enter the clinic this year and next. 2 0 1 5 A N N UA L R E P O R T 14 < M E N U >

FOS T ERING T HE FU T URE OF SCIEN T IFIC INNOVAT ION We believe our STEM (Science, Technology, Engineering and Math) education is a top priority; we are focused on ensuring a strong pipeline of STEM talent for many years to come. Spanning from elementary school to postdoctoral fellowships, our STEM programs spark interest in science and enhance knowledge, scientific research and careers in biotechnology. AT T R AC T, SU P P OR T A ND R E WA R D the bes t and brightes t minds in science research Our immersive internship program offers college and graduate students a uniquely collaborative work environment to gain hands-on, real-world experience. We are also a founding supporter and title sponsor of the Westchester Science and Engineering Fair (affiliated with the International Science and Engineering Fair, or ISEF) high school science research competition, and award the Regeneron Prize to graduate and postdoctoral students every year. I N C R E A SE T HE EFFEC T I V ENE S S of teacher s in S T E M Created in partnership with the STEM Leadership Center, our teaching fellowship gives New York state-certified middle and high school science teachers the tools they need to deliver higher-quality instruction. B R I D G E S T EM SK I L L S G A P S A ND C A R EER AWA R ENE S S among s tudent s his torically under represented in the sciences Our Sci2Med Academy initiative with Yonkers Partners in Education is an after-school program for high school juniors that broadens knowledge of science and awareness of careers in biotechnology. Students have the opportunity to learn about biotechnology and drug discovery, hear from Regeneron researchers and tour the labs. Science Education hours: 19,000 Number of REGN Interns: 196 2 0 1 5 A N N UA L R E P O R T 20 < M E N U >

CULT IVAT ING SUS TA IN A BLE COMMUNI T IES We proudly support the communities where we work and live, and that includes a company-wide commitment to environmental sustainability. 2,118 600 93 % Community Service Regeneron in the Community (RIC), our company volunteer program, unites our people through days of service, company-sponsored activities and employee-led projects. RIC inspires action, fosters collaboration and motivates our people to self-organize around service projects that reflect their individual passions. 66 volunteer hours at organizations through RIC additional organizations supported through the Matching Gifts Program of employees feel good about the ways w e contribute to the community — Great Places to Work Employee Survey Environmental Sustainability We want to grow our business while reducing our environmental impact. We proactively seek environmentally responsible ways to better operate our business now and in the future, and we focus on environmental stewardship throughout our value chain. In 2013, we set five-year targets in four key areas to help inform our choices and actions, all with the aim of reducing our environmental footprint as we grow. C A RBON * Reduced our carbon footprint per employee by 14%, moving toward our expanded 2018 goal of 30% EL E C T RICI T Y* Reduced our consumption per employee by 5%, moving toward our 2018 goal of 10% WA S T E 44% of our waste avoids the landfill, moving toward our 2018 goal of 90% H A Z A RDOUS CHEMIC A L WA S T E 51% reduction per lab employee, just short of our 2018 goal of 60% *Carbon and Electricity are reported based on the Carbon Disclosure Project reporting year; 2013 noted above corresponds to June 2013 – May 2014 reporting year. 2 0 1 5 A N N UA L R E P O R T 21 < M E N U >

SUPPOR T ING PAT IEN T COMMUNI T IES Our employees are focused on putting science, technology and innovation to work to make a difference in patients’ lives. This effort starts in the labs, moves into the clinic and continues with our commitment to ensuring patients can access the therapies they need. Comprehensive patient programs, like MyPraluent™ and EYLEA4USM, provide support for patients throughout their treatment journey by offering insurance eligibility support, financial assistance and free medicine to eligible patients. Additional services include access to educational information and clinical support for physicians, nurses and pharmacists. Regeneron does not influence or control the operations of independent co-pay assistance foundations and cannot guarantee assistance will be provided. We also aim to support and active engagement the patients we serve. community needs through unique programs with the advocacy organizations that represent ITNAmerica/Rides in Sight Regeneron is a national Eye-Care Services Sponsor for ITNAmerica /Rides in Sight. Advocacy Partnerships Our company was built on the fundamental goal of helping patients, and we regularly engage with advocacy organizations to help empower patients. For example, we partnered with the Arthritis Foundation to create patient advocacy summits and patient ambassador ITNAmerica is the first, national non-profit transportation network committed to providing safe, low-cost, community-based transportation options for seniors and those with vision loss to help them maintain their independence. programs, all with the goal of catalyzing national and local advocacy efforts. 2 0 1 5 A N N UA L R E P O R T 22 < M E N U >

NUR T URING OUR HIGH - ENGAGEMEN T, HIGH - IN T EGRI T Y CULT URE We empower our people to thrive personally and professionally, work together to create inclusion. positive change, and promote an ethical culture of diversity and 4TH Most Innovative Company, according to Forbes 2ND 5 YRS 95% CONSECUTIVE YEAR of employees say “I’m proud to tell others I 100 Best Companies to Work For, Fortune Ranked #1 or #2 employer in the global biopharmaceutical industry in Science Top Employers Survey 5 years in a row work here” - Great Places to Work Employee Survey We work hard to nurture our highly ethical culture through: Integrity at Work We pride ourselves on doing the right thing and have rigorous policies in place to ensure that our colleagues, vendors and business partners are acting in accordance with all applicable laws, rules and regulations. Opportunities for Growth We encourage and assist our employees in their quests to continue learning throughout their careers. Culture of Collaboration We thrive on diverse ideas and individuals who aren’t afraid to challenge convention, and we believe our next great discovery could spring from any level of the organization. 2 0 1 5 A N N UA L R E P O R T 23 < M E N U >

FORWA RD - LOOK ING S TAT EMEN T S 2 0 1 5 A N N UA L R E P O R T 24 < M E N U > This Annual Report includes forward-looking statements that involve risks and uncertainties relating to future events and the future performance of Regeneron Pharmaceuticals, Inc. (“we,” “us,” “our,” “Regeneron,” or the “Company”), and actual events or results may differ materially from these forward-looking statements. Words such as “anticipate,” “expect,” “intend,” “plan,” “believe,” “seek,” “estimate,” variations of such words and similar expressions are intended to identify such forward-looking statements, although not all forward-looking statements contain these identifying words. These statements concern, and these risks and uncertainties include, among others, the nature, timing, and possible success and therapeutic applications of our products, product candidates, and research and clinical programs now underway or planned, including without limitation EYLEA® (aflibercept) Injection, PRALUENT® (alirocumab) Injection, sarilumab, dupilumab, fasinumab, REGN 2222, and the immuno-oncology program; unforeseen safety issues resulting from the administration of products and product candidates in patients, including serious complications or side effects in connection with the use of our product candidates in clinical trials; the likelihood and timing of possible regulatory approval and commercial launch of our late-stage product candidates and new indications for marketed products, including without limitation EYLEA®, PRALUENT®, sarilumab, dupilumab, fasinumab, and REGN 2222; ongoing regulatory obligations and oversight impacting our marketed products (such as EYLEA® and PRALUENT®), research and clinical programs, and business, including those relating to patient privacy; determinations by regulatory and administrative governmental authorities which may delay or restrict our ability to continue to develop or commercialize our products and product candidates; competing drugs and product candidates that may be superior to our products and product candidates; uncertainty of market acceptance and commercial success of our products and product candidates; our ability to manufacture and manage supply chains for multiple products and product candidates; coverage and reimbursement determinations by third-party payers, including Medicare and Medicaid; unanticipated expenses; the costs of developing, producing, and selling products; our ability to meet any of its sales or other financial projections or guidance and changes to the assumptions underlying those projections or guidance; the potential for any license or collaboration agreement, including our agreements with Sanofi and Bayer HealthCare LLC, to be canceled or terminated without any further product success; and risks associated with third-party intellectual property and pending or future litigation relating thereto. A more complete description of these and other material risks can be found in our filings with the Securities and Exchange Commission, including our Annual Report on Form 10-K for the fiscal year ended December 31, 2015 (filed with the Securities and Exchange Commission on February 11, 2016), including in the section thereof captioned “Item 1A. Risk Factors.” Any forward-looking statements are made based on management’s current beliefs and judgment, and the reader is cautioned not to rely on any forward-looking statements made by Regeneron. We do not undertake any obligation to update publicly any forward-looking statement, including without limitation any financial projection or guidance, whether as a result of new information, future events, or otherwise.

CORPOR AT E INFORM AT ION 2 0 1 5 A N N UA L R E P O R T 25 < M E N U > Common Stock and Related Matters Our Common Stock is traded on The NASDAQ Global Select Market under the symbol “REGN.” Our Class A Stock is not publicly quoted or traded. The following table sets forth, for the periods indicated, the range of high and low sales prices for the Common Stock as reported by The NASDAQ Global Select Market. 2014HIGH LOW 2015HIGH LOW First Quarter$ 352.49$262.97First Quarter$495.50$ 393.00 Second Quarter$ 320.00$269.50Second Quarter$ 544.00$433.47 Third Quarter$ 369.31$285.06Third Quarter$ 605.93$435.52 Fourth Quarter$437.64$ 320.06Fourth Quarter$ 592.59$488.10 As of April 14, 2016, there were 211 shareholders of record of our Common Stock and 23 shareholders of record of our Class A Stock. The closing sales price for the Common Stock on that date was $406.83. We have never paid cash dividends and do not anticipate paying any in the foreseeable future. SEC Form 10-K 2016 Annual Shareholder Meeting A copy of our 2015 Annual Report on Form 10-K filed with the Securities and ExchangeThe 2016 Annual Shareholder Meeting will be held on Commission (which accompanies and forms part of this 2015 Annual Report to Shareholders) isFriday, June 10, 2016, at 10:30 a.m. at the Westchester available without charge from the Regeneron Investor Relations Department. Marriott Hotel, 670 White Plains Road, Tarrytown, New York 10591. Shareholders’ Inquiries Inquiries relating to stock transfer or lost certificates and notices of changes of address should be directed to our Transfer Agent, American Stock Transfer & Trust Co., 6201 15th Avenue, Brooklyn, New York 11219, (800) 937-5449, www.amstock.com/main. General information regarding the Company, recent press releases, and SEC filings are available on our website at www.regeneron.com, or can be obtained by contacting our Investor Relations Department at (914) 847-7741. Corporate Office Transfer Agent and Registrar Independent Registered Public Accounting Firm 777 Old Saw Mill River RoadAmerican Stock Transfer & Trust Co. PricewaterhouseCoopers LLP Tarrytown, New York 10591-6707 6201 15th Avenue (914) 847-7400 Brooklyn, New York 11219 REGENERON®, Science to Medicine®, and the following are registered trademarks of Regeneron Pharmaceuticals, Inc.: ARCALYST®, EYLEA®, VelociGene®, and VelocImmune®. PRALUENT® is a registered trademark of Sanofi.

REFERENCES 2 0 1 5 A N N UA L R E P O R T 26 < M E N U 1.American College of Rheumatology. “Rheumatoid Arthritis.” 8. Maggio M, et al. J Gerontol A Biol Sci Med Sci. 2006;61(6):575-584. Available at: http://www.rheumatology.org/I-Am-A/Patient-9.Garnero P, et al. Arthritis Rheum. 2010;62(1):33-43. Caregiver/Diseases-Conditions/Rheumatoid-Arthritis. 10. Ishimi Y, et al. J Immunol. 1990;145(10):3297-3303. Last accessed: September 2015.11. Choy EH, et al. Nat Rev Rheumatol. 2013;9 (3):154-163. 2.Choy E. Rheumatology (Oxford). 2012;51(suppl 5):v3-v11.12. Bartok B, et al. Immunol Rev. 2010;233(1):233-255. 3. Dayer JM, et al. Rheumatology (Oxford). 2010;49 (1):15-24.13. Adelphi Final Report 2014/2015, data on file. 4. Ito A, et al. Arthritis Rheum. 1992;35(10):1197-1201.14. Centers for Disease Control and Prevention. “Infection and Incidence.” 5. Wong PK, et al. Arthritis Rheum. 2006;54(1):158-168.Available at: http://www.cdc.gov/rsv/about/infection.html. 6. McInnes IB. Cytokines. In: Firestein GS, Budd RC, Gabriel SE,Last accessed: March 2016. McInnes IB, O’Dell JR, eds. Kelley’s Textbook of Rheumatology.15. American Pain Society, “Estimates of Pain Prevalence and Severity in Vol 1. 9th ed. Philadelphia, PA: Elsevier/Saunders; 2013:369-381. Adults: United States, 2012.” Available at http://www.jpain.org/article/ 7.Saxena A, Cronstein BN. In: Firestein GS, Budd RC, Gabriel SE,S1526-5900 (15) 00679-3/pdf. Last accessed: March 2016. McInnes IB, O’Dell JR, eds. Kelley’s Textbook of Rheumatology. Vol 1. 9th ed. Philadelphia, PA: Elsevier/Saunders; 2013:818-829.