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Q3 2014 RESULTS 
October 28, 2014
2 
Forward Looking Statements 
This presentation contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. These statements include projections and estimates and their underlying assumptions, statements regarding plans, objectives, intentions and expectations with respect to future financial results, events, operations, services, product development and potential, and statements regarding future performance. Forward-looking statements are generally identified by the words "expects", "anticipates", "believes", "intends", "estimates", "plans" and similar expressions. Although Sanofi's management believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Sanofi, that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include among other things, the uncertainties inherent in research and development, future clinical data and analysis, including post marketing, decisions by regulatory authorities, such as the FDA or the EMA, regarding whether and when to approve any drug, device or biological application that may be filed for any such product candidates as well as their decisions regarding labeling and other matters that could affect the availability or commercial potential of such product candidates, the absence of guarantee that the product candidates if approved will be commercially successful, the future approval and commercial success of therapeutic alternatives, the Group's ability to benefit from external growth opportunities, trends in exchange rates and prevailing interest rates, the impact of cost containment policies and subsequent changes thereto, the average number of shares outstanding as well as those discussed or identified in the public filings with the SEC and the AMF made by Sanofi, including those listed under "Risk Factors" and "Cautionary Statement Regarding Forward-Looking Statements" in Sanofi's annual report on Form 20-F for the year ended December 31, 2013. Other than as required by applicable law, Sanofi does not undertake any obligation to update or revise any forward-looking information or statements.
3 
Agenda 
Key Highlights 
● 
Christopher A. Viehbacher, Chief Executive Officer 
Financial Performance 
● 
Jérôme Contamine, Executive Vice President, Chief Financial Officer 
Conclusion 
● 
Christopher A. Viehbacher, Chief Executive Officer 
Q&A
KEY HIGHLIGHTS 
4 
Christopher A. Viehbacher 
Chief Executive Officer
● 
Net sales up +5.1% at CER(1) 
● 
Business EPS up +10.3% at CER(1) 
● 
Free Cash Flow up +15.8% in 9M 2014 
● 
78.1% of Group sales and up +10.0% at CER despite more challenging U.S. diabetes market dynamics 
● 
Vaccines sales returned to growth 
● 
Animal Health sales grew double digit 
● 
Global licensing agreement for Afrezza® 
● 
U.S. approval of Cerdelga™ for Gaucher disease 
● 
Major positive Phase III readouts on alirocumab and Dengue vaccine 
● 
Start of Phase III with dupilumab in Atopic Dermatitis 
Sanofi Delivered Another Solid Quarter in Q3 2014 
5 
3 
2 
1 
Solid financial performance 
Strong performance of Growth Platforms 
Bringing new medicines to market 
(1) 
On a reported basis, Q3 2014 sales were up +4.1% and Business EPS was up +8.1%
Q3 2014 
FX Impact 
-€0.03 
Incremental EPS at CER 
+€0.14 
Q3 2013 
Net Sales 
Business EPS 
Successful Growth Strategy Continues to Deliver Solid Top and Bottom Line Growth in Q3 2014 
6 
(1) 
On a reported basis, Q3 2014 sales were up +4.1% and Business EPS was up +8.1% 
(2)With retroactive application of IFRIC21 
+10.3% at CER(1) 
Q3 2014 
FX Impact 
-€81m 
Incremental Sales at CER 
+€430m 
Q3 2013 
+5.1% at CER(1) 
€8,432m 
€8,781m 
€1.36 
€1.47 
(2) 
(2)
Quarterly Sales Growth from Growth Platforms(1) 
+10.0% 
Q3 2013 
+5.5% 
Q2 2013 
+6.2% 
Q1 2013 
+8.6% 
Q4 2012 
+11.5% 
Q3 2012 
+6.4% 
Q2 2012 
+7.6% 
Q1 2012 
+5.7% 
10.0% 
Q2 2014 
Q3 2014 
Q1 2014 
10.7% 
+7.9% 
Q4 2013 
(1) 
Growth at CER. Q1 2012 growth restated for Genzyme Q1 2011 (€396m) 
(2) 
Growth at CER including Generics in Brazil was +2.5% in Q2 2013 and +14.5% in Q2 2014 7 
Consistent Strong Sales Performance of Growth Platforms Demonstrates the Sustainability of our Business Model 
+5% at CER 
+10% at CER 
% of Group sales 
63.2% 
78.1% 
(2) 
(2)
Vaccines 
+11.2% 
Consumer Healthcare(3) 
€1,451m 
-4.2% 
€819m 
Genzyme(4) 
Growth Platforms Grew +10.0%(1) in Q3 2014 Now Representing As Much As 78.1% of Sales 8 
(1) 
Excluding Generics in Brazil, Growth Platforms grew +9.1% in 9M 2014 at CER 
(2) 
Excluding Generics in Brazil, Emerging Markets grew +6.1% in 9M 2014 at CER 
(3) 
Some products recorded in prescription pharmaceuticals in 2013 were transferred as Consumer Healthcare products and totaled €64m in Q3 2013 and €205m in 9M 2014. When including this category change, sales of Consumer Healthcare grew +4.0% in Q3 2014 and +7.6% in 9M 2014 at CER 
(4) 
Genzyme perimeter includes Rare Diseases and Multiple Sclerosis franchises 
(5) 
Includes products launched since 2009 which do not belong to the Growth Platforms listed above: Multaq®, Jevtana®, Auvi-Q™, Mozobil® and Zaltrap® 
+8.3% 
+12.9% 
+24.6% 
+12.7% 
Other Innovative Products(5) 
€227m 
+7.6% 
Diabetes Solutions 
€1,799m 
Animal Health 
€649m 
Emerging Markets(2) 
€2,776m 
€515m 
Q3 2014 Sales & Growth at CER 
-4.2% 
9M 2014 Sales & Growth at CER 
+4.1% 
+12.5% 
+17.3% 
+25.1% 
+5.3% 
+17.9% 
+9.9% 
€2,797m 
€2,520m 
€606m 
€5,249m 
€1,858m 
€8,221m 
€1,569m 
+18.0%
Strong U.S. Formulary Access Secured in Q3 2014 in an Increasingly Competitive Pricing Environment 
9 
Quarterly Sales (€m) 
Q1 
2013 
Q2 
2013 
Q3 
2013 
Q4 
2013 
Q1 
2014 
Q2 
2014 
Q3 
2014 
€1,567m 
● 
Lantus® sales up +8.1% at CER 
● 
Up +9.5% in Western Europe and +19.7% in Emerging Markets at CER 
● 
U.S. growth of +5.8% at CER reflecting increasing competitive pressure at the payor level and impact of the Affordable Care Act 
● 
Favorable Lantus® formulary positions secured in recent U.S. payor negotiations 
● 
Significant increase of rebates due to aggressive discounting by competition 
● 
>90% unrestricted coverage in commercial and non-commercial channels 
● 
Sanofi total diabetes sales expected to be broadly stable in 2015 
Regulatory decisions for Toujeo® expected in H1 2015 in the U.S. & EU
Strong Performance of Sanofi Pasteur in Q3 2014 in Line with Expectations 
● 
Strong Flu vaccines sales up +15.0% at CER driven by successful differentiation strategy in the U.S. 
● 
Other vaccines sales up +8.4% at CER given recovery in Pentacel® sales due to improved supply 
● 
Several R&D milestones achieved: 
● 
Successful completion of Phase III program for first ever Dengue vaccine 
● 
Submission of PR5i in the U.S.(1) 
● 
Phase III start with Shantha’s investigational Rotavirus vaccine 
Sales 
Q3 2014 
€1,451m 
FX 
€5m 
Other Vaccines 
€62m 
Flu 
€84m 
Q3 2013 
€1,300m 
+11.2% 
at CER(1) 
(1) 
PR5i is an investigational pediatric hexavalent vaccine, DTaP5-IPV-Hib-HepB, developed by Merck and Sanofi Pasteur 10
Q1 
2013 
Q2 
2013 
Q3 
2013 
Q4 
2013 
Q1 
2014 
Q2 
2014 
Q3 
2014 
Genzyme’s Aubagio® Continues to See Expanded Use 
Quarterly Sales (€m) 
€112m 
● 
Continued solid sales ramp up of once-daily Aubagio® 
● 
Results from 2 Phase III studies added to U.S. label of Aubagio® 
● 
Only oral treatment to significantly slow progression of disability in 2 Phase III in RMS (TEMSO and TOWER) and to have positive data on early MS (TOPIC) in its label 
● 
Label expansion in EU expected in Q4 2014 following positive CHMP opinion in Sep 2014 (TOWER and TOPIC) 
RMS: Relapsing Multiple Sclerosis 
U.S. regulatory decision for Lemtrada™ expected in Q4 2014 
11
Merial Delivers Strong Growth in Q3 2014 
12 
● 
Strong sales up +12.7% at CER 
● 
Double digit growth in Companion as well as Production Animals 
● 
Successful launch of NexGard™ 
● 
New soft, beef-flavored chew treating fleas and ticks for dogs with sales of €85m in 9M 2014 
● 
Solid performance of Heartgard® and pet vaccines in Q3 2014 
Q1 
2013 
Q2 
2013 
Q3 
2013 
Q4 
2013 
Q1 
2014 
Q2 
2014 
Q3 
2014 
-3.1% 
-5.7% 
-6.3% 
Merial Sales Growth at CER 
-6.4% 
-1.6% 
+12.7% 
+6.2%
Significant Progress in Q3 2014 in Advancing New Medicines and Vaccines Closer to Launch 
13 
● 
9 positive Phase III top-line readouts announced in Q3 2014 
● 
Priority review voucher in the U.S. 
● 
U.S. and EU regulatory submissions expected by end of 2014 
● 
FDA approval granted in August 2014 and U.S. launch underway 
● 
CHMP opinion expected in Q4 2014 
● 
Positive 2nd Phase III results in LatAm released in September 2014 
● 
Regulatory submissions in priority countries expected as of Q1 2015 
● 
Start of Phase III in AD in late Q3 2014 
● 
Positive PoC top-line results in Nasal Polyposis announced in Q3 2014 
● 
Phase IIb headline results in Moderate to Severe Asthma expected in Q4 2014 
- AD / NP / Asthma 
Alirocumab and dupilumab are developed in collaboration with Regeneron 
PoC: Proof-of-Concept AD: Atopic Dermatitis NP/ Nasal Polyposis 
- Gaucher Disease 
- Hypercholesterolemia 
R&D 
Dengue Vaccine
● 
Afrezza® has the potential to address resistance to insulin initiation and insulin intensification, a major problem in the suboptimal treatment of diabetes 
●PK profile of Afrezza®, a rapid-acting inhaled insulin, can simulate the natural prandial insulin response 
●Inhaler is an innovative, unique and patient friendly device that helps patients overcome many of the barriers to insulin treatment 
●Launch of Afrezza® in the U.S. is expected in Q1 2015 
14 
Global Licensing Agreement with Mannkind for Afrezza® in Q3 2014 Expands Diabetes Portfolio
Innovation Momentum Set to Continue in Q4 2014 
15 
2014 
Expected Regulatory Decisions 
Q3 
Q4 
● 
Cerdelga™ (eliglustat) in Gaucher disease (U.S.) 
● 
Lemtrada™ (alemtuzumab) in Multiple Sclerosis (U.S.) 
 
● 
Cerdelga™ (eliglustat) in Gaucher disease (EU) 
 
● 
Fluzone® QIV Intradermal (U.S.) 
 
Expected Regulatory Submissions 
Q3 
Q4 
● 
PR5i 6-in-1 pediatric vaccine (U.S.) 
● 
Alirocumab in Hypercholesterolemia (U.S. & EU) 
 
Expected Headline Phase III Data Releases 
Q3 
Q4 
● 
Alirocumab in Hypercholesterolemia (9 ODYSSEY trials) 
● 
Dengue vaccine 2nd Phase III trial in Latin America 
Expected Phase III Starts 
Q3 
Q4 
● 
Dupilumab in Atopic Dermatitis 
● 
Rotavirus vaccine 
● 
Insulin lispro in Diabetes 

FINANCIAL PERFORMANCE 
Jérôme Contamine 
Executive Vice President, Chief Financial Officer 
16
Net Sales(1) 
Business EPS 
17 
Limited FX Impact in Q3 2014 Given Strengthening of U.S. Dollar 
(1) 
Main currency impact on sales in Q3 2014: Argentine Peso (-€26.0m); Japanese Yen (-€24.8m); Russian Ruble (-€21.1m) 
(2) 
Difference between variation on reported basis and variation at constant exchange rates. Assuming September 2014 average exchange rates remain stable till end of 2014, the negative foreign currency impact on FY 2014 would be 2 and 3% on sales and between 3 and 4% on business EPS. 
Quarterly Currency Impact 
-2.5% 
-€212m 
-4.4% 
-€0.08 
-3.5% 
-€305m 
-€0.08 
-5.5% 
-7.3% 
-€662m 
-€0.17 
-10.2% 
2013 
Q4 
Q3 
Q2 
Q1 
-7.3% 
-€627m 
2014 
Q1 
-€0.16 
-13.7% 
-6.2% 
-€497m 
-9.1% 
-€0.11 
Assuming September 2014 exchange rates remain stable in Q4 2014, the foreign currency impact on Q4 2014 business EPS is expected to turn positive2) 
Q2 
-5.5% 
-€443m 
2014 
Q1 
Q2 
-8.9% 
-€0.10 
-1.0% 
-€81m 
Q3 
-€0.03 
-2.2% 
Q3 
2013 
Q4 
Q3 
Q2 
Q1
(1) 
With the retroactive application of IFRIC21 
(2) 
Includes a payment of €40m before tax resulting from the termination of the license of a U.S. product 18 
BOI Increased Faster than Sales Again in Q3 2014 
€m 
Q3 2014 
Q3 2013 
% Change (reported €) 
% Change (CER) 
Net sales 
8,781 
8,432 
+4.1% 
+5.1% 
Other revenues 
87 
86 
+1.2% 
- 
Cost of sales 
(2,864) 
(2,870) 
-0.2% 
+0.7% 
Gross profit 
6,004 
5,648 
+6.3% 
+7.3% 
R&D 
(1 146) 
(1,182) 
-3.0% 
-2.6% 
SG&A 
(2,193) 
(2,012) 
+9.0% 
+10.0% 
Other current operating income & expenses 
39 
28 
- 
- 
Share of Profit/Loss of associates 
43 
38 
- 
- 
Minority interests 
(31) 
(36) 
- 
- 
Business operating income 
2,716 
2,484 
+9.3% 
+11.0% 
Business operating margin 
30.9% 
29.5% 
CER: Constant Exchange Rates 
(1) 
(2)
Improvement in Gross Margin in Q3 2014 vs. Q3 2013 
●Stable Cost of Sales (CoS) of €2,864m in Q3 2014 (+0.7% at CER) 
●Gross margin up 1.4 percentage point in Q3 2014 vs. Q3 2013 
●Recovery from Sanofi Pasteur manufacturing issues in Toronto 
●Improved industrial performance of Genzyme and Aubagio® sales 
●Positive mix effects in the U.S. and China 
19 
Gross Margin (%) 
Q1 
Q2 
Q3 
Q4 
Q1 
Q2 
Q3 
2013 
2014 
67.0% 
68.4% 
(1) 
With retroactive application of IFRIC21 
(1)
R&D Expenses Slightly Decreased in Q3 2014 
20 
●Q3 2014 R&D expenses of €1,146m, down -2.6% at CER reflecting: 
●Lower expenses in Oncology 
●Completion of EDITION program with Toujeo® in Diabetes 
●More than offsetting higher spend on dupilumab clinical development 
Q1 
Q2 
Q3 
Q4 
Q1 
Q2 
Q3 
R&D Expenses (€m) 
€1,146m 
€1,182m 
(1) 
2013 
2014 
(1) 
With retroactive application of IFRIC21
Higher SG&A to Sales Ratio in Q3 2014 vs. Q3 2013 
21 
●Q3 2014 SG&A expenses of €2,193m, up +10.0% at CER 
●SG&A increase driven by: 
●Rebound from a low base for commercial activities in China 
●Higher A&P spend in the U.S. on NexGard™ and Frontline® 
●Genzyme launch investments in MS and Rare Diseases 
●Higher global pre-marketing costs 
SG&A Expenses (€m) 
Q1 
Q2 
Q3 
Q4 
Q1 
Q2 
Q3 
€2,193m 
€2,012m 
(1) 
2013 
2014 
(1) 
With retroactive application of IFRIC21
CER: Constant Exchange Rates 
22 
€m 
Q3 2014 
Q3 2013 
% Change (reported €) 
% Change (CER) 
Business operating income 
2,716 
2,484 
+9.3% 
+11.0% 
Net financial expenses 
(139) 
(123) 
+13.0% 
+15.4% 
Income tax expense 
(642) 
(566) 
+13.4% 
+15.0% 
Effective tax rate 
-25.0% 
-24.0% 
- 
- 
Business net income 
1,935 
1,795 
+7.8% 
+9.4% 
Net margin 
22.0% 
21.3% 
Business EPS 
€1.47 
€1.36 
+8.1% 
+10.3% 
Average number of shares outstanding (m) 
1,313.0 
1,323.5 
- 
- 
Strong Business EPS Growth of +10.3% in Q3 2014 
(1) 
With the retroactive application of IFRIC21 
(1)
Net Debt (in €m) 
Net Debt Sep 30, 2014 
Other 
-€1,061m 
Dividend 
-€3,676m 
Acquisitions, Licensing, Net of Disposals 
-€2,220m 
Net Debt Dec 31, 2013 
Proceeds from Issuance of Shares 
-€1,102m 
€635m 
CapEx 
-€802m 
Net Cash from Operating Activities 
Share Repurchase 
Free Cash Flow (FCF) Increased by 15.8% in 9M 2014 
23 
(1) 
(2) 
€6,043m 
€9,228m 
€5,041m 
(4) 
(1) 
FCF €4,239m 
FCF: Free Cash Flow 
(1) 
Including derivatives related to the financial debt +€290m at December 31st 2013 and +€323m at September 30th 2014 
(2) 
Excluding Restructuring costs 
(3) 
Including €1,492m in Regeneron and €535m in Alnylam 
(4) 
Other including Restructuring costs 
(3)
CONCLUSION 
24 
Christopher A. Viehbacher 
Chief Executive Officer
Solid Performance in 9M 2014 Reflects Consistent Execution of our Growth Strategy 
Solid sales and business EPS growth in Q3 2014 
Growth platforms up +10.0% at CER and accounting for 78.1% of sales despite tougher U.S. diabetes market dynamics 
Business EPS guidance for 2014 reconfirmed given solid performance year to date and strong base for comparison in Q4(1) 
Significant advances in bringing new medicines to market 
25 
IR Thematic Seminar on New Medicines and Vaccines on Nov 20th 
(1)Q4 2013 financial results included receipt of a payment of €92m before tax following the amendment of the Actonel® agreement with Warner Chilcott and an income of €93m before tax resulting from the Rituxan® arbitration between Hoechst and Genentech
APPENDICES R&D Pipeline 
26
27 
Late Stage Pipeline – Pharma & Vaccines 
LixiLan lixisenatide + insulin glargine Fixed-Ratio / Type 2 diabetes 
alirocumab Anti-PCSK-9 mAb Hypercholesterolemia 
Dengue Mild-to-severe dengue fever vaccine 
Toujeo® (U300) 
Insulin glargine Type 1+2 diabetes, U.S., EU 
Lyxumia® (lixisenatide) GLP-1 agonist Type 2 diabetes, U.S. 
Kynamro® (mipomersen) 
Apolipoprotein B-100 antisense 
Severe HeFH, U.S. 
Clostridium difficile Toxoid vaccine 
Lemtrada™ (alemtuzumab) 
Anti-CD52 mAb 
Multiple sclerosis, U.S. 
sarilumab Anti-IL-6R mAb Rheumatoid arthritis 
Jevtana® (cabazitaxel) Metastatic prostate cancer (1L) 
Rotavirus Live attenuated tetravalent Rotavirus oral vaccine 
Cerdelga™ (eliglustat tartrate) 
Glucosylceramide synthetase inhibitor 
Gaucher disease, EU 
dupilumab Anti-IL4Rα mAb Atopic dermatitis 
SYNVISC-ONE® 
Medical device 
Pain in hip OA 
VaxiGrip® QIV IM Quadrivalent inactivated influenza vaccine 
PR5i 
DTP-HepB-Polio-Hib Pediatric hexavalent vaccine, U.S. 
patisiran mRNA inhibitor Familial amyloid polyneuropathy 
Fluzone® QIV ID Quadrivalent inactivated influenza vaccine intradermal 
Quadracel® Diphtheria, tetanus, pertussis & polio vaccine; 4-6 y of age 
N 
N 
N 
N 
N 
New Molecular Entity 
Immune Mediated Diseases 
Rare Diseases 
Oncology 
Diabetes Solutions 
Vaccines 
Infectious Diseases 
Cardiovascular / Renal Diseases 
Age Related Degenerative Diseases 
Ophthalmology 
Biosurgery 
N 
Phase III 
Registration 
N 
N
Early Stage Pipeline – Pharma & Vaccines 
dupilumab Anti-IL4Rα mAb Asthma; Nasal polyposis 
SAR391786 Anti-GDF8 mAb 
Sarcopenia 
Rabies VRVg Purified vero rabies vaccine 
valetizumab Anti-VLA 2 mAb Multiple sclerosis 
SAR650984 Anti-CD38 naked mAb Multiple myeloma 
Meningitis ACYW conj. 2nd generation meningococcal conjugate infant vaccine 
SAR156597 IL4/IL13 Bi-specific mAb Idiopathic pulmonary fibrosis 
SAR3419 Maytansin-loaded anti-CD19 mAb B-cell refractory/relapsed malignancies 
Tuberculosis Recombinant subunit vaccine 
SAR438714 (ALN-TTRsc) 
RNAi 
Familial amyloid cardiomyopathy 
Combination SAR245409 (XL765) / MSC1936369B 
Oral dual inhibitor of PI3K & mTOR / pimasertib Ovarian cancer 
sarilumab Anti-IL-6R mAb Uveitis 
Combination ferroquine / OZ439 Antimalarial Malaria 
fresolimumab 
TGFβ antagonist 
Focal segmental glomerulosclerosis 
Phase II 
N 
N 
N 
N 
N 
28 
N 
N 
N 
New Molecular Entity 
Immune Mediated Diseases 
Rare Diseases 
Oncology 
Diabetes Solutions 
Vaccines 
Infectious Diseases 
Cardiovascular / Renal Diseases 
Age Related Degenerative Diseases 
Ophthalmology 
Biosurgery 
N 
N
Early Stage Pipeline – Pharma & Vaccines 
SAR405838 (MI-773) HDM2 / p53 antagonist 
Solid tumors 
SAR408701 Anti-CEACAM5 ADC Solid tumors 
GZ402663 (sFLT-01) Gene therapy Age-related macular degeneration (AMD) 
Streptococcus pneumonia Meningitis & pneumonia vaccine 
SAR566658 Maytansin-loaded anti-CA6 mAb Solid tumors 
SAR113244 Anti-CXCR5 mAb 
Systemic lupus erythematosus 
StarGen® Gene therapy Stargardt disease 
Herpes Simplex Virus Type 2 HSV-2 vaccine 
SAR125844 C-MET kinase inhibitor Solid tumors 
SAR252067 Anti-LIGHT mAb Crohn’s disease 
UshStat® Gene therapy Usher syndrome 1B 
SAR260301 PI3K β selective inhibitor PTEN – Deficient tumors 
SAR228810 Anti-protofibrillar AB mAb Alzheimer’s disease 
GZ402665 (rhASM) Niemann-Pick type B 
SAR307746 Anti-ANG2 mAb Solid tumors 
SAR425899 
GLP-1 / GCGR agonist 
Diabetes 
GZ402671 
Oral GCS Inhibitor 
Fabry Disease 
SAR245408 (XL147) Oral PI3K inhibitor Solid tumors 
SAR342434 Insulin Lispro Diabetes 
GZ402666 
neo GAA Pompe Disease 
Combination SAR405838 / MSC1936369B Solid tumors 
SAR438584 (REGN2222) anti-RSV-F protein mAb 
Respiratory syncytial virus 
Phase I 
N 
N 
N 
N 
N 
N 
N 
N 
N 
N 
N 
N 
29 
N 
N 
N 
New Molecular Entity 
Immune Mediated Diseases 
Rare Diseases 
Oncology 
Diabetes Solutions 
Vaccines 
Infectious Diseases 
Cardiovascular / Renal Diseases 
Age Related Degenerative Diseases 
Ophthalmology 
Biosurgery 
N 
N 
N 
N
30 
Phase I 
Phase II 
Phase III 
Registration 
TOTAL 
Oncology 
7 
3 
0 
0 
10 
Diabetes Solutions 
1 
0 
1 
1 
3 
Cardiovascular / Renal Diseases 
0 
1 
1 
0 
2 
Immune Mediated Diseases 
2 
2 
2 
0 
6 
Infectious Diseases 
1 
1 
0 
0 
2 
Ophthalmology 
3 
0 
0 
0 
3 
Rare Diseases 
3 
1 
1 
1 
6 
Age Related Degenerative Diseases 
1 
1 
0 
0 
2 
Vaccines 
2 
3 
4 
3 
12 
TOTAL 
20 
12 
9 
5 
R&D Pipeline Summary Table(1) 
32 
14 
NMEs & Vaccines 
46 
34 
(1) 
Excluding life cycle management programs
31 
Expected R&D Milestones in Q4 2014 / H1 2015 
Product 
Event 
Timing 
Dupilumab (anti-IL4Rα mAb) 
Start of Phase III trial in Atopic Dermatitis 
Q3 2014 
Rotavirus vaccine 
Start of Phase III trial 
Q4 2014 
New Insulin Lispro (SAR342434) 
Expected start of Phase III trial in Diabetes 
Q4 2014 
Lemtrada™ (alemtuzumab) 
Expected U.S. regulatory decision in Multiple Sclerosis 
Q4 2014 
Cerdelga™ (eliglustat tartrate) 
Expected EU regulatory decision in Gaucher disease 
Q4 2014 
Alirocumab (anti-PCSK9 mAb) 
Expected U.S. and EU regulatory submissions in Hypercholesterolemia 
Q4 2014 
Fluzone® QIV ID 
Expected U.S. regulatory decision 
Q4 2014 
Fluzone® High Dose 
Expected U.S. label upgrade 
Q4 2014 
Dupilumab (anti-IL4Rα mAb) 
Expected Phase IIb top-line results in Asthma 
Q4 2014 
Dengue vaccine 
Expected regulatory submission in priority countries 
Q1 2015 
PR5i (DTP-HepB-Polio-Hib) 
Expected EU regulatory submission 
Q1 2015 
Quadracel® 
Expected U.S. regulatory decision 
Q1 2015 
Toujeo® (U300) 
Expected U.S. regulatory decisions in Diabetes 
Q1 2015 
Toujeo® (U300) 
Expected EU regulatory decisions in Diabetes 
Q2 2015 
Lyxumia® (lixisenatide) 
Expected ELIXA CV outcome trial top-line results 
Q2 2015
APPENDICES FINANCE 
32
33 
Business Net Income Statement 
Third quarter 2014 
Group Total 
Pharmaceuticals 
Vaccines 
Animal Health 
Others 
€ million 
Q3 2014 
Q3 2013(1) 
Change 
Q3 2014 
Q3 2013(1) 
Change 
Q3 2014 
Q3 2013(1) 
Change 
Q3 2014 
Q3 2013(1) 
Change 
Q3 2014 
Q3 2013(1) 
Net sales 
8,781 
8,432 
4.1% 
6,815 
6,674 
2.1% 
1,451 
1,300 
11.6% 
515 
458 
12.4% 
- 
- 
Other revenues 
87 
86 
1.2% 
69 
69 
- 
9 
9 
- 
9 
8 
12.5% 
- 
- 
Cost of sales 
(2,864) 
(2,870) 
(0.2%) 
(2,036) 
(2,133) 
(4.5%) 
(629) 
(580) 
8.4% 
(199) 
(157) 
26.8% 
- 
- 
As % of net sales 
(32.6%) 
(34.0%) 
(29.9%) 
(32.0%) 
(43.3%) 
(44.6%) 
(38.6%) 
(34.2%) 
Gross profit 
6,004 
5,648 
6.3% 
4,848 
4,610 
5.2% 
831 
729 
14.0% 
325 
309 
5.2% 
- 
- 
As % of net sales 
68.4% 
67.0% 
71.1% 
69.1% 
57.3% 
56.1% 
63.1% 
67.5% 
Research and development expenses 
(1,146) 
(1,182) 
(3.0%) 
(987) 
(1,011) 
(2.4%) 
(121) 
(133) 
(9.0%) 
(38) 
(38) 
- 
- 
- 
As % of net sales 
(13.1%) 
(14.0%) 
(14.5%) 
(15.1%) 
(8.3%) 
(10.2%) 
(7.4%) 
(8.3%) 
Selling and general expenses 
(2,193) 
(2,012) 
9.0% 
(1,859) 
(1,706) 
9.0% 
(170) 
(154) 
10.4% 
(164) 
(152) 
7.9% 
- 
- 
As % of net sales 
(25.0%) 
(23.9%) 
(27.3%) 
(25.6%) 
(11.7%) 
(11.8%) 
(31.8%) 
(33.2%) 
Other current operating income/expenses 
39 
28 
57 
33 
2 
(1) 
1 
(1) 
(21) 
(3) 
Share of profit/loss of associates* and joint ventures 
43 
38 
22 
3 
21 
36 
- 
(1) 
- 
- 
Net income attributable to non-controlling interests 
(31) 
(36) 
(31) 
(37) 
- 
1 
- 
- 
- 
- 
Business operating income 
2,716 
2,484 
9.3% 
2,050 
1,892 
8.4% 
563 
478 
17.8% 
124 
117 
6.0% 
(21) 
(3) 
As % of net sales 
30.9% 
29.5% 
30.1% 
28.3% 
38.8% 
36.8% 
24.1% 
25.5% 
Financial income and expenses 
(139) 
(123) 
Income tax expense 
(642) 
(566) 
Tax rate** 
25.0% 
24.0% 
Business net income 
1,935 
1,795 
7.8% 
As % of net sales 
22.0% 
21.3% 
Business earnings per share*** (in euros) 
1.47 
1.36 
8.1% 
* Net of tax. ** Determined on the basis of Business income before tax, associates and non-controlling interests. *** Based on an average number of shares outstanding of 1,313.0 million in the third quarter of 2014 and 1,323.5 million in the third quarter of 2013. (1) Including impact of transition to IFRIC 21.
34 
Business Net Income Statement 
Nine months 2014 
Group Total 
Pharmaceuticals 
Vaccines 
Animal Health 
Others 
€ million 
9M 2014 
9M 2013(1) 
Change 
9M 2014 
9M 2013(1) 
Change 
9M 2014 
9M 2013(1) 
Change 
9M 2014 
9M 2013(1) 
Change 
9M 2014 
9M 2013(1) 
Net sales 
24,698 
24,494 
0.8% 
20,332 
20,196 
0.7% 
2,797 
2,757 
1.5% 
1,569 
1,541 
1.8% 
- 
- 
Other revenues 
241 
267 
(9.7%) 
195 
224 
(12.9%) 
23 
21 
9.5% 
23 
22 
4.5% 
- 
- 
Cost of sales 
(7,988) 
(8,085) 
(1.2%) 
(6,082) 
(6,307) 
(3.6%) 
(1,329) 
(1,275) 
4.2% 
(577) 
(503) 
14.7% 
- 
- 
As % of net sales 
(32.4%) 
(33.0%) 
(29.9%) 
(31.2%) 
(47.5%) 
(46.3%) 
(36.8%) 
(32.6%) 
Gross profit 
16,951 
16,676 
1.6% 
14,445 
14,113 
2.4% 
1,491 
1,503 
(0.8%) 
1,015 
1,060 
(4.2%) 
- 
- 
As % of net sales 
68.6% 
68.1% 
71.0% 
69.9% 
53.3% 
54.5% 
64.7% 
68.8% 
Research and development expenses 
(3,473) 
(3,524) 
(1.4%) 
(3,012) 
(3,019) 
(0.2%) 
(351) 
(382) 
(8.1%) 
(110) 
(123) 
(10.6%) 
- 
- 
As % of net sales 
(14.1%) 
(14.4%) 
(14.8%) 
(14.9%) 
(12.5%) 
(13.9%) 
(7.0%) 
(8.0%) 
Selling and general expenses 
(6,526) 
(6,458) 
1.1% 
(5,580) 
(5,507) 
1.3% 
(441) 
(455) 
(3.1%) 
(505) 
(496) 
1.8% 
- 
- 
As % of net sales 
(26.4%) 
(26.4%) 
(27.4%) 
(27.3%) 
(15.8%) 
(16.5%) 
(32.2%) 
(32.2%) 
Other current operating income/expenses 
68 
198 
76 
163 
3 
6 
18 
(2) 
(29) 
31 
Share of profit/loss of associates* and joint ventures 
82 
59 
55 
30 
27 
32 
- 
(3) 
- 
- 
Net income attributable to non-controlling interests 
(96) 
(122) 
(96) 
(123) 
- 
1 
- 
- 
- 
- 
Business operating income 
7,006 
6,829 
2.6% 
5,888 
5,657 
4.1% 
729 
705 
3.4% 
418 
436 
(4.1%) 
(29) 
31 
As % of net sales 
28.4% 
27.9% 
29.0% 
28.0% 
26.1% 
25.6% 
26.6% 
28.3% 
Financial income and expenses 
(309) 
(400) 
Income tax expense 
(1,678) 
(1,557) 
Tax rate** 
25.0% 
24.0% 
Business net income 
5,019 
4,872 
3.0% 
As % of net sales 
20.3% 
19.9% 
Business earnings per share*** (in euros) 
3.81 
3.68 
3.5% 
* Net of tax. ** Determined on the basis of Business income before tax, associates and non-controlling interests. *** Based on an average number of shares outstanding of 1,315.8 million in the first nine months of 2014 and 1,323.8 million in the first nine months of 2013. (1) Including impact of transition to IFRIC 21
Reconciliation of Business Net Income to Consolidated Net Income Attributable to Equity Holders of Sanofi 
35 
€ million 
Q3 2014 
Q3 2013(1) 
Change 
Business net income 
1,935 
1,795 
7.8% 
Amortization of intangible assets(2) 
(561) 
(689) 
Impairment of intangible assets 
(35) 
(28) 
Fair value remeasurement of contingent consideration liabilities 
(45) 
(68) 
Expenses arising from the impact of acquisitions on inventories 
- 
(1) 
Restructuring costs 
(163) 
(71) 
Additional year expense related to US Branded Prescription Drug Fee(3) 
(116) 
- 
Tax effect of items listed above: 
261 
289 
Amortization of intangible assets 
188 
233 
Impairment of intangible assets 
13 
9 
Fair value remeasurement of contingent consideration liabilities 
5 
23 
Expenses arising from the impact of acquisitions on inventories 
- 
- 
Restructuring costs 
55 
24 
Other tax items 
- 
- 
Share of items listed above attributable to non-controlling interests 
- 
1 
Restructuring costs of associates and joint ventures, and expenses arising from the impact of acquisitions on associates and joint ventures 
(86) 
(9) 
Net income attributable to equity holders of Sanofi 
1,190 
1,219 
(2.4%) 
Consolidated earnings per share(4) (in euros) 
0.91 
0.92 
(1) 
Including impact of transition to IFRIC 21 
(2) 
Of which related to amortization expense generated by the remeasurement of intangible assets as part of business combinations: €540 million in the third quarter of 2014 and €658 million in the third quarter of 2013. 
(3) 
Annual fee related to 2013 sales in the U.S. following the final IRS regulation issued in July 2014 that has changed the timing of liability recognition and leads to a one-time “double” expense in the year of 2014. 
(4) 
Based on an average number of shares outstanding of 1,313.0 million in the third quarter of 2014 and 1,323.5 in the third quarter of 2013.
Reconciliation of Business Net Income to Consolidated Net Income Attributable to Equity Holders of Sanofi 
36 
(1) 
Including impact of transition to IFRIC 21. 
(2) 
Of which related to amortization expense generated by the remeasurement of intangible assets as part of business combinations: €1,798 million in the first nine months of 2014 and €2,147 million in the first nine months of 2013. 
(3) 
Day one profit on Alnylam shares presented in financial result. 
(4) 
Annual fee related to 2013 sales following the final IRS regulation issued in July 2014 that has changed the timing of liability recognition and leads to a one-time “double” expense in the year of 2014. 
(5) 
Tax on dividends paid to shareholders of Sanofi. 
(6) 
Based on an average number of shares outstanding of 1,315.8 million in the first nine months of 2014 and 1,323.8 million in the first nine months of 2013. 
€ million 
9M 2014 
9M 2013(1) 
Change 
Business net income 
5,019 
4,872 
3.0% 
Amortization of intangible assets(2) 
(1,862) 
(2,232) 
Impairment of intangible assets 
(109) 
(468) 
Fair value remeasurement of contingent consideration liabilities 
(177) 
(185) 
Expenses arising from the impact of acquisitions on inventories 
- 
(7) 
Restructuring costs 
(298) 
(230) 
Other gains and losses, and litigation(3) 
35 
- 
Additional year expense related to US Branded Prescription Drug Fee(4) 
(116) 
- 
Tax effect of items listed above: 
783 
1,038 
Amortization of intangible assets 
639 
723 
Impairment of intangible assets 
39 
189 
Fair value remeasurement of contingent consideration liabilities 
19 
43 
Expenses arising from the impact of acquisitions on inventories 
- 
2 
Other gains and losses, and litigation 
(13) 
- 
Restructuring costs 
99 
81 
Other tax items(5) 
(110) 
(109) 
Share of items listed above attributable to non-controlling interests 
4 
3 
Restructuring costs of associates and joint ventures. and expenses arising from the impact of acquisitions on associates and joint ventures 
(118) 
(26) 
Net income attributable to equity holders of Sanofi 
3,051 
2,656 
14.9% 
Consolidated earnings per share(6) (in euros) 
2.32 
2.01
37 
Consolidated Income Statements 
€ million 
Q3 2014 
Q3 2013(1) 
9M 2014 
9M 2013(1) 
Net sales 
8,781 
8,432 
24,698 
24,494 
Other revenues 
87 
86 
241 
267 
Cost of sales 
(2,864) 
(2,871) 
(7,988) 
(8,092) 
Gross profit 
6,004 
5,647 
16,951 
16,669 
Research and development expenses 
(1,146) 
(1,182) 
(3,473) 
(3,524) 
Selling and general expenses 
(2,309) 
(2,012) 
(6,642) 
(6,458) 
Other operating income 
47 
56 
163 
403 
Other operating expenses 
(8) 
(28) 
(95) 
(205) 
Amortization of intangible assets 
(561) 
(689) 
(1,862) 
(2,232) 
Impairment of intangible assets 
(35) 
(28) 
(109) 
(468) 
Fair value remeasurement of contingent consideration liabilities 
(45) 
(68) 
(177) 
(185) 
Restructuring costs 
(163) 
(71) 
(298) 
(230) 
Operating income 
1,784 
1,625 
4,458 
3,770 
Financial expenses 
(154) 
(147) 
(446) 
(458) 
Financial income 
15 
24 
172 
58 
Income before tax and associates and joint ventures 
1,645 
1,502 
4,184 
3,370 
Income tax expense(2) 
(381) 
(277) 
(1,005) 
(628) 
Share of profit/loss of associates and joint ventures 
(43) 
29 
(36) 
33 
Net income 
1,221 
1,254 
3,143 
2,775 
Net income attributable to non-controlling interests 
31 
35 
92 
119 
Net income attributable to equity holders of Sanofi 
1,190 
1,219 
3,051 
2,656 
Average number of shares outstanding (million) 
1,313.0 
1,323.5 
1,315.8 
1,323.8 
Earnings per share (in euros) 
0.91 
0.92 
2.32 
2.01 
(1) 
Including impact of transition to IFRIC 21. 
(2) 
In 2014, including a tax on dividends paid to shareholders of Sanofi: (110) M€ compared to (109) M€ in 2013.
Business EPS Currency Sensitivity 
€ 23.1% 
US $ 37.3% 
Japanese Yen 5.5% 
£ 2.2% 
Australian $ 1.6% 
Canadian $ 1.5% 
Brazilian Real 3.5% 
Chinese Yuan 4.3% 
Russian Ruble 2.2% 
Others 16.8% 
Mexican Peso 2.0% 
Currency Exposure on Q3 2014 Sales 
Currency Average Rates 
2014 Currency Sensitivity 
38 
● 
1% variation in €/$ corresponds to an impact of 0.5% on 2014 Business EPS 
●1% variation in €/Yen corresponds to an impact of 0.1% on 2014 Business EPS 
Q3 2013 
Q3 2014 
% change 
€/$ 
1.32 
1.33 
+0.8% 
€/Yen 
131.05 
137.74 
+5.1% 
€/Real 
3.03 
3.01 
-0.7% 
€/Ruble 
43.45 
48.08 
+10.7%

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Q3 2014 RESULTS by sanofi

  • 1. Q3 2014 RESULTS October 28, 2014
  • 2. 2 Forward Looking Statements This presentation contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. These statements include projections and estimates and their underlying assumptions, statements regarding plans, objectives, intentions and expectations with respect to future financial results, events, operations, services, product development and potential, and statements regarding future performance. Forward-looking statements are generally identified by the words "expects", "anticipates", "believes", "intends", "estimates", "plans" and similar expressions. Although Sanofi's management believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Sanofi, that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include among other things, the uncertainties inherent in research and development, future clinical data and analysis, including post marketing, decisions by regulatory authorities, such as the FDA or the EMA, regarding whether and when to approve any drug, device or biological application that may be filed for any such product candidates as well as their decisions regarding labeling and other matters that could affect the availability or commercial potential of such product candidates, the absence of guarantee that the product candidates if approved will be commercially successful, the future approval and commercial success of therapeutic alternatives, the Group's ability to benefit from external growth opportunities, trends in exchange rates and prevailing interest rates, the impact of cost containment policies and subsequent changes thereto, the average number of shares outstanding as well as those discussed or identified in the public filings with the SEC and the AMF made by Sanofi, including those listed under "Risk Factors" and "Cautionary Statement Regarding Forward-Looking Statements" in Sanofi's annual report on Form 20-F for the year ended December 31, 2013. Other than as required by applicable law, Sanofi does not undertake any obligation to update or revise any forward-looking information or statements.
  • 3. 3 Agenda Key Highlights ● Christopher A. Viehbacher, Chief Executive Officer Financial Performance ● Jérôme Contamine, Executive Vice President, Chief Financial Officer Conclusion ● Christopher A. Viehbacher, Chief Executive Officer Q&A
  • 4. KEY HIGHLIGHTS 4 Christopher A. Viehbacher Chief Executive Officer
  • 5. ● Net sales up +5.1% at CER(1) ● Business EPS up +10.3% at CER(1) ● Free Cash Flow up +15.8% in 9M 2014 ● 78.1% of Group sales and up +10.0% at CER despite more challenging U.S. diabetes market dynamics ● Vaccines sales returned to growth ● Animal Health sales grew double digit ● Global licensing agreement for Afrezza® ● U.S. approval of Cerdelga™ for Gaucher disease ● Major positive Phase III readouts on alirocumab and Dengue vaccine ● Start of Phase III with dupilumab in Atopic Dermatitis Sanofi Delivered Another Solid Quarter in Q3 2014 5 3 2 1 Solid financial performance Strong performance of Growth Platforms Bringing new medicines to market (1) On a reported basis, Q3 2014 sales were up +4.1% and Business EPS was up +8.1%
  • 6. Q3 2014 FX Impact -€0.03 Incremental EPS at CER +€0.14 Q3 2013 Net Sales Business EPS Successful Growth Strategy Continues to Deliver Solid Top and Bottom Line Growth in Q3 2014 6 (1) On a reported basis, Q3 2014 sales were up +4.1% and Business EPS was up +8.1% (2)With retroactive application of IFRIC21 +10.3% at CER(1) Q3 2014 FX Impact -€81m Incremental Sales at CER +€430m Q3 2013 +5.1% at CER(1) €8,432m €8,781m €1.36 €1.47 (2) (2)
  • 7. Quarterly Sales Growth from Growth Platforms(1) +10.0% Q3 2013 +5.5% Q2 2013 +6.2% Q1 2013 +8.6% Q4 2012 +11.5% Q3 2012 +6.4% Q2 2012 +7.6% Q1 2012 +5.7% 10.0% Q2 2014 Q3 2014 Q1 2014 10.7% +7.9% Q4 2013 (1) Growth at CER. Q1 2012 growth restated for Genzyme Q1 2011 (€396m) (2) Growth at CER including Generics in Brazil was +2.5% in Q2 2013 and +14.5% in Q2 2014 7 Consistent Strong Sales Performance of Growth Platforms Demonstrates the Sustainability of our Business Model +5% at CER +10% at CER % of Group sales 63.2% 78.1% (2) (2)
  • 8. Vaccines +11.2% Consumer Healthcare(3) €1,451m -4.2% €819m Genzyme(4) Growth Platforms Grew +10.0%(1) in Q3 2014 Now Representing As Much As 78.1% of Sales 8 (1) Excluding Generics in Brazil, Growth Platforms grew +9.1% in 9M 2014 at CER (2) Excluding Generics in Brazil, Emerging Markets grew +6.1% in 9M 2014 at CER (3) Some products recorded in prescription pharmaceuticals in 2013 were transferred as Consumer Healthcare products and totaled €64m in Q3 2013 and €205m in 9M 2014. When including this category change, sales of Consumer Healthcare grew +4.0% in Q3 2014 and +7.6% in 9M 2014 at CER (4) Genzyme perimeter includes Rare Diseases and Multiple Sclerosis franchises (5) Includes products launched since 2009 which do not belong to the Growth Platforms listed above: Multaq®, Jevtana®, Auvi-Q™, Mozobil® and Zaltrap® +8.3% +12.9% +24.6% +12.7% Other Innovative Products(5) €227m +7.6% Diabetes Solutions €1,799m Animal Health €649m Emerging Markets(2) €2,776m €515m Q3 2014 Sales & Growth at CER -4.2% 9M 2014 Sales & Growth at CER +4.1% +12.5% +17.3% +25.1% +5.3% +17.9% +9.9% €2,797m €2,520m €606m €5,249m €1,858m €8,221m €1,569m +18.0%
  • 9. Strong U.S. Formulary Access Secured in Q3 2014 in an Increasingly Competitive Pricing Environment 9 Quarterly Sales (€m) Q1 2013 Q2 2013 Q3 2013 Q4 2013 Q1 2014 Q2 2014 Q3 2014 €1,567m ● Lantus® sales up +8.1% at CER ● Up +9.5% in Western Europe and +19.7% in Emerging Markets at CER ● U.S. growth of +5.8% at CER reflecting increasing competitive pressure at the payor level and impact of the Affordable Care Act ● Favorable Lantus® formulary positions secured in recent U.S. payor negotiations ● Significant increase of rebates due to aggressive discounting by competition ● >90% unrestricted coverage in commercial and non-commercial channels ● Sanofi total diabetes sales expected to be broadly stable in 2015 Regulatory decisions for Toujeo® expected in H1 2015 in the U.S. & EU
  • 10. Strong Performance of Sanofi Pasteur in Q3 2014 in Line with Expectations ● Strong Flu vaccines sales up +15.0% at CER driven by successful differentiation strategy in the U.S. ● Other vaccines sales up +8.4% at CER given recovery in Pentacel® sales due to improved supply ● Several R&D milestones achieved: ● Successful completion of Phase III program for first ever Dengue vaccine ● Submission of PR5i in the U.S.(1) ● Phase III start with Shantha’s investigational Rotavirus vaccine Sales Q3 2014 €1,451m FX €5m Other Vaccines €62m Flu €84m Q3 2013 €1,300m +11.2% at CER(1) (1) PR5i is an investigational pediatric hexavalent vaccine, DTaP5-IPV-Hib-HepB, developed by Merck and Sanofi Pasteur 10
  • 11. Q1 2013 Q2 2013 Q3 2013 Q4 2013 Q1 2014 Q2 2014 Q3 2014 Genzyme’s Aubagio® Continues to See Expanded Use Quarterly Sales (€m) €112m ● Continued solid sales ramp up of once-daily Aubagio® ● Results from 2 Phase III studies added to U.S. label of Aubagio® ● Only oral treatment to significantly slow progression of disability in 2 Phase III in RMS (TEMSO and TOWER) and to have positive data on early MS (TOPIC) in its label ● Label expansion in EU expected in Q4 2014 following positive CHMP opinion in Sep 2014 (TOWER and TOPIC) RMS: Relapsing Multiple Sclerosis U.S. regulatory decision for Lemtrada™ expected in Q4 2014 11
  • 12. Merial Delivers Strong Growth in Q3 2014 12 ● Strong sales up +12.7% at CER ● Double digit growth in Companion as well as Production Animals ● Successful launch of NexGard™ ● New soft, beef-flavored chew treating fleas and ticks for dogs with sales of €85m in 9M 2014 ● Solid performance of Heartgard® and pet vaccines in Q3 2014 Q1 2013 Q2 2013 Q3 2013 Q4 2013 Q1 2014 Q2 2014 Q3 2014 -3.1% -5.7% -6.3% Merial Sales Growth at CER -6.4% -1.6% +12.7% +6.2%
  • 13. Significant Progress in Q3 2014 in Advancing New Medicines and Vaccines Closer to Launch 13 ● 9 positive Phase III top-line readouts announced in Q3 2014 ● Priority review voucher in the U.S. ● U.S. and EU regulatory submissions expected by end of 2014 ● FDA approval granted in August 2014 and U.S. launch underway ● CHMP opinion expected in Q4 2014 ● Positive 2nd Phase III results in LatAm released in September 2014 ● Regulatory submissions in priority countries expected as of Q1 2015 ● Start of Phase III in AD in late Q3 2014 ● Positive PoC top-line results in Nasal Polyposis announced in Q3 2014 ● Phase IIb headline results in Moderate to Severe Asthma expected in Q4 2014 - AD / NP / Asthma Alirocumab and dupilumab are developed in collaboration with Regeneron PoC: Proof-of-Concept AD: Atopic Dermatitis NP/ Nasal Polyposis - Gaucher Disease - Hypercholesterolemia R&D Dengue Vaccine
  • 14. ● Afrezza® has the potential to address resistance to insulin initiation and insulin intensification, a major problem in the suboptimal treatment of diabetes ●PK profile of Afrezza®, a rapid-acting inhaled insulin, can simulate the natural prandial insulin response ●Inhaler is an innovative, unique and patient friendly device that helps patients overcome many of the barriers to insulin treatment ●Launch of Afrezza® in the U.S. is expected in Q1 2015 14 Global Licensing Agreement with Mannkind for Afrezza® in Q3 2014 Expands Diabetes Portfolio
  • 15. Innovation Momentum Set to Continue in Q4 2014 15 2014 Expected Regulatory Decisions Q3 Q4 ● Cerdelga™ (eliglustat) in Gaucher disease (U.S.) ● Lemtrada™ (alemtuzumab) in Multiple Sclerosis (U.S.)  ● Cerdelga™ (eliglustat) in Gaucher disease (EU)  ● Fluzone® QIV Intradermal (U.S.)  Expected Regulatory Submissions Q3 Q4 ● PR5i 6-in-1 pediatric vaccine (U.S.) ● Alirocumab in Hypercholesterolemia (U.S. & EU)  Expected Headline Phase III Data Releases Q3 Q4 ● Alirocumab in Hypercholesterolemia (9 ODYSSEY trials) ● Dengue vaccine 2nd Phase III trial in Latin America Expected Phase III Starts Q3 Q4 ● Dupilumab in Atopic Dermatitis ● Rotavirus vaccine ● Insulin lispro in Diabetes 
  • 16. FINANCIAL PERFORMANCE Jérôme Contamine Executive Vice President, Chief Financial Officer 16
  • 17. Net Sales(1) Business EPS 17 Limited FX Impact in Q3 2014 Given Strengthening of U.S. Dollar (1) Main currency impact on sales in Q3 2014: Argentine Peso (-€26.0m); Japanese Yen (-€24.8m); Russian Ruble (-€21.1m) (2) Difference between variation on reported basis and variation at constant exchange rates. Assuming September 2014 average exchange rates remain stable till end of 2014, the negative foreign currency impact on FY 2014 would be 2 and 3% on sales and between 3 and 4% on business EPS. Quarterly Currency Impact -2.5% -€212m -4.4% -€0.08 -3.5% -€305m -€0.08 -5.5% -7.3% -€662m -€0.17 -10.2% 2013 Q4 Q3 Q2 Q1 -7.3% -€627m 2014 Q1 -€0.16 -13.7% -6.2% -€497m -9.1% -€0.11 Assuming September 2014 exchange rates remain stable in Q4 2014, the foreign currency impact on Q4 2014 business EPS is expected to turn positive2) Q2 -5.5% -€443m 2014 Q1 Q2 -8.9% -€0.10 -1.0% -€81m Q3 -€0.03 -2.2% Q3 2013 Q4 Q3 Q2 Q1
  • 18. (1) With the retroactive application of IFRIC21 (2) Includes a payment of €40m before tax resulting from the termination of the license of a U.S. product 18 BOI Increased Faster than Sales Again in Q3 2014 €m Q3 2014 Q3 2013 % Change (reported €) % Change (CER) Net sales 8,781 8,432 +4.1% +5.1% Other revenues 87 86 +1.2% - Cost of sales (2,864) (2,870) -0.2% +0.7% Gross profit 6,004 5,648 +6.3% +7.3% R&D (1 146) (1,182) -3.0% -2.6% SG&A (2,193) (2,012) +9.0% +10.0% Other current operating income & expenses 39 28 - - Share of Profit/Loss of associates 43 38 - - Minority interests (31) (36) - - Business operating income 2,716 2,484 +9.3% +11.0% Business operating margin 30.9% 29.5% CER: Constant Exchange Rates (1) (2)
  • 19. Improvement in Gross Margin in Q3 2014 vs. Q3 2013 ●Stable Cost of Sales (CoS) of €2,864m in Q3 2014 (+0.7% at CER) ●Gross margin up 1.4 percentage point in Q3 2014 vs. Q3 2013 ●Recovery from Sanofi Pasteur manufacturing issues in Toronto ●Improved industrial performance of Genzyme and Aubagio® sales ●Positive mix effects in the U.S. and China 19 Gross Margin (%) Q1 Q2 Q3 Q4 Q1 Q2 Q3 2013 2014 67.0% 68.4% (1) With retroactive application of IFRIC21 (1)
  • 20. R&D Expenses Slightly Decreased in Q3 2014 20 ●Q3 2014 R&D expenses of €1,146m, down -2.6% at CER reflecting: ●Lower expenses in Oncology ●Completion of EDITION program with Toujeo® in Diabetes ●More than offsetting higher spend on dupilumab clinical development Q1 Q2 Q3 Q4 Q1 Q2 Q3 R&D Expenses (€m) €1,146m €1,182m (1) 2013 2014 (1) With retroactive application of IFRIC21
  • 21. Higher SG&A to Sales Ratio in Q3 2014 vs. Q3 2013 21 ●Q3 2014 SG&A expenses of €2,193m, up +10.0% at CER ●SG&A increase driven by: ●Rebound from a low base for commercial activities in China ●Higher A&P spend in the U.S. on NexGard™ and Frontline® ●Genzyme launch investments in MS and Rare Diseases ●Higher global pre-marketing costs SG&A Expenses (€m) Q1 Q2 Q3 Q4 Q1 Q2 Q3 €2,193m €2,012m (1) 2013 2014 (1) With retroactive application of IFRIC21
  • 22. CER: Constant Exchange Rates 22 €m Q3 2014 Q3 2013 % Change (reported €) % Change (CER) Business operating income 2,716 2,484 +9.3% +11.0% Net financial expenses (139) (123) +13.0% +15.4% Income tax expense (642) (566) +13.4% +15.0% Effective tax rate -25.0% -24.0% - - Business net income 1,935 1,795 +7.8% +9.4% Net margin 22.0% 21.3% Business EPS €1.47 €1.36 +8.1% +10.3% Average number of shares outstanding (m) 1,313.0 1,323.5 - - Strong Business EPS Growth of +10.3% in Q3 2014 (1) With the retroactive application of IFRIC21 (1)
  • 23. Net Debt (in €m) Net Debt Sep 30, 2014 Other -€1,061m Dividend -€3,676m Acquisitions, Licensing, Net of Disposals -€2,220m Net Debt Dec 31, 2013 Proceeds from Issuance of Shares -€1,102m €635m CapEx -€802m Net Cash from Operating Activities Share Repurchase Free Cash Flow (FCF) Increased by 15.8% in 9M 2014 23 (1) (2) €6,043m €9,228m €5,041m (4) (1) FCF €4,239m FCF: Free Cash Flow (1) Including derivatives related to the financial debt +€290m at December 31st 2013 and +€323m at September 30th 2014 (2) Excluding Restructuring costs (3) Including €1,492m in Regeneron and €535m in Alnylam (4) Other including Restructuring costs (3)
  • 24. CONCLUSION 24 Christopher A. Viehbacher Chief Executive Officer
  • 25. Solid Performance in 9M 2014 Reflects Consistent Execution of our Growth Strategy Solid sales and business EPS growth in Q3 2014 Growth platforms up +10.0% at CER and accounting for 78.1% of sales despite tougher U.S. diabetes market dynamics Business EPS guidance for 2014 reconfirmed given solid performance year to date and strong base for comparison in Q4(1) Significant advances in bringing new medicines to market 25 IR Thematic Seminar on New Medicines and Vaccines on Nov 20th (1)Q4 2013 financial results included receipt of a payment of €92m before tax following the amendment of the Actonel® agreement with Warner Chilcott and an income of €93m before tax resulting from the Rituxan® arbitration between Hoechst and Genentech
  • 27. 27 Late Stage Pipeline – Pharma & Vaccines LixiLan lixisenatide + insulin glargine Fixed-Ratio / Type 2 diabetes alirocumab Anti-PCSK-9 mAb Hypercholesterolemia Dengue Mild-to-severe dengue fever vaccine Toujeo® (U300) Insulin glargine Type 1+2 diabetes, U.S., EU Lyxumia® (lixisenatide) GLP-1 agonist Type 2 diabetes, U.S. Kynamro® (mipomersen) Apolipoprotein B-100 antisense Severe HeFH, U.S. Clostridium difficile Toxoid vaccine Lemtrada™ (alemtuzumab) Anti-CD52 mAb Multiple sclerosis, U.S. sarilumab Anti-IL-6R mAb Rheumatoid arthritis Jevtana® (cabazitaxel) Metastatic prostate cancer (1L) Rotavirus Live attenuated tetravalent Rotavirus oral vaccine Cerdelga™ (eliglustat tartrate) Glucosylceramide synthetase inhibitor Gaucher disease, EU dupilumab Anti-IL4Rα mAb Atopic dermatitis SYNVISC-ONE® Medical device Pain in hip OA VaxiGrip® QIV IM Quadrivalent inactivated influenza vaccine PR5i DTP-HepB-Polio-Hib Pediatric hexavalent vaccine, U.S. patisiran mRNA inhibitor Familial amyloid polyneuropathy Fluzone® QIV ID Quadrivalent inactivated influenza vaccine intradermal Quadracel® Diphtheria, tetanus, pertussis & polio vaccine; 4-6 y of age N N N N N New Molecular Entity Immune Mediated Diseases Rare Diseases Oncology Diabetes Solutions Vaccines Infectious Diseases Cardiovascular / Renal Diseases Age Related Degenerative Diseases Ophthalmology Biosurgery N Phase III Registration N N
  • 28. Early Stage Pipeline – Pharma & Vaccines dupilumab Anti-IL4Rα mAb Asthma; Nasal polyposis SAR391786 Anti-GDF8 mAb Sarcopenia Rabies VRVg Purified vero rabies vaccine valetizumab Anti-VLA 2 mAb Multiple sclerosis SAR650984 Anti-CD38 naked mAb Multiple myeloma Meningitis ACYW conj. 2nd generation meningococcal conjugate infant vaccine SAR156597 IL4/IL13 Bi-specific mAb Idiopathic pulmonary fibrosis SAR3419 Maytansin-loaded anti-CD19 mAb B-cell refractory/relapsed malignancies Tuberculosis Recombinant subunit vaccine SAR438714 (ALN-TTRsc) RNAi Familial amyloid cardiomyopathy Combination SAR245409 (XL765) / MSC1936369B Oral dual inhibitor of PI3K & mTOR / pimasertib Ovarian cancer sarilumab Anti-IL-6R mAb Uveitis Combination ferroquine / OZ439 Antimalarial Malaria fresolimumab TGFβ antagonist Focal segmental glomerulosclerosis Phase II N N N N N 28 N N N New Molecular Entity Immune Mediated Diseases Rare Diseases Oncology Diabetes Solutions Vaccines Infectious Diseases Cardiovascular / Renal Diseases Age Related Degenerative Diseases Ophthalmology Biosurgery N N
  • 29. Early Stage Pipeline – Pharma & Vaccines SAR405838 (MI-773) HDM2 / p53 antagonist Solid tumors SAR408701 Anti-CEACAM5 ADC Solid tumors GZ402663 (sFLT-01) Gene therapy Age-related macular degeneration (AMD) Streptococcus pneumonia Meningitis & pneumonia vaccine SAR566658 Maytansin-loaded anti-CA6 mAb Solid tumors SAR113244 Anti-CXCR5 mAb Systemic lupus erythematosus StarGen® Gene therapy Stargardt disease Herpes Simplex Virus Type 2 HSV-2 vaccine SAR125844 C-MET kinase inhibitor Solid tumors SAR252067 Anti-LIGHT mAb Crohn’s disease UshStat® Gene therapy Usher syndrome 1B SAR260301 PI3K β selective inhibitor PTEN – Deficient tumors SAR228810 Anti-protofibrillar AB mAb Alzheimer’s disease GZ402665 (rhASM) Niemann-Pick type B SAR307746 Anti-ANG2 mAb Solid tumors SAR425899 GLP-1 / GCGR agonist Diabetes GZ402671 Oral GCS Inhibitor Fabry Disease SAR245408 (XL147) Oral PI3K inhibitor Solid tumors SAR342434 Insulin Lispro Diabetes GZ402666 neo GAA Pompe Disease Combination SAR405838 / MSC1936369B Solid tumors SAR438584 (REGN2222) anti-RSV-F protein mAb Respiratory syncytial virus Phase I N N N N N N N N N N N N 29 N N N New Molecular Entity Immune Mediated Diseases Rare Diseases Oncology Diabetes Solutions Vaccines Infectious Diseases Cardiovascular / Renal Diseases Age Related Degenerative Diseases Ophthalmology Biosurgery N N N N
  • 30. 30 Phase I Phase II Phase III Registration TOTAL Oncology 7 3 0 0 10 Diabetes Solutions 1 0 1 1 3 Cardiovascular / Renal Diseases 0 1 1 0 2 Immune Mediated Diseases 2 2 2 0 6 Infectious Diseases 1 1 0 0 2 Ophthalmology 3 0 0 0 3 Rare Diseases 3 1 1 1 6 Age Related Degenerative Diseases 1 1 0 0 2 Vaccines 2 3 4 3 12 TOTAL 20 12 9 5 R&D Pipeline Summary Table(1) 32 14 NMEs & Vaccines 46 34 (1) Excluding life cycle management programs
  • 31. 31 Expected R&D Milestones in Q4 2014 / H1 2015 Product Event Timing Dupilumab (anti-IL4Rα mAb) Start of Phase III trial in Atopic Dermatitis Q3 2014 Rotavirus vaccine Start of Phase III trial Q4 2014 New Insulin Lispro (SAR342434) Expected start of Phase III trial in Diabetes Q4 2014 Lemtrada™ (alemtuzumab) Expected U.S. regulatory decision in Multiple Sclerosis Q4 2014 Cerdelga™ (eliglustat tartrate) Expected EU regulatory decision in Gaucher disease Q4 2014 Alirocumab (anti-PCSK9 mAb) Expected U.S. and EU regulatory submissions in Hypercholesterolemia Q4 2014 Fluzone® QIV ID Expected U.S. regulatory decision Q4 2014 Fluzone® High Dose Expected U.S. label upgrade Q4 2014 Dupilumab (anti-IL4Rα mAb) Expected Phase IIb top-line results in Asthma Q4 2014 Dengue vaccine Expected regulatory submission in priority countries Q1 2015 PR5i (DTP-HepB-Polio-Hib) Expected EU regulatory submission Q1 2015 Quadracel® Expected U.S. regulatory decision Q1 2015 Toujeo® (U300) Expected U.S. regulatory decisions in Diabetes Q1 2015 Toujeo® (U300) Expected EU regulatory decisions in Diabetes Q2 2015 Lyxumia® (lixisenatide) Expected ELIXA CV outcome trial top-line results Q2 2015
  • 33. 33 Business Net Income Statement Third quarter 2014 Group Total Pharmaceuticals Vaccines Animal Health Others € million Q3 2014 Q3 2013(1) Change Q3 2014 Q3 2013(1) Change Q3 2014 Q3 2013(1) Change Q3 2014 Q3 2013(1) Change Q3 2014 Q3 2013(1) Net sales 8,781 8,432 4.1% 6,815 6,674 2.1% 1,451 1,300 11.6% 515 458 12.4% - - Other revenues 87 86 1.2% 69 69 - 9 9 - 9 8 12.5% - - Cost of sales (2,864) (2,870) (0.2%) (2,036) (2,133) (4.5%) (629) (580) 8.4% (199) (157) 26.8% - - As % of net sales (32.6%) (34.0%) (29.9%) (32.0%) (43.3%) (44.6%) (38.6%) (34.2%) Gross profit 6,004 5,648 6.3% 4,848 4,610 5.2% 831 729 14.0% 325 309 5.2% - - As % of net sales 68.4% 67.0% 71.1% 69.1% 57.3% 56.1% 63.1% 67.5% Research and development expenses (1,146) (1,182) (3.0%) (987) (1,011) (2.4%) (121) (133) (9.0%) (38) (38) - - - As % of net sales (13.1%) (14.0%) (14.5%) (15.1%) (8.3%) (10.2%) (7.4%) (8.3%) Selling and general expenses (2,193) (2,012) 9.0% (1,859) (1,706) 9.0% (170) (154) 10.4% (164) (152) 7.9% - - As % of net sales (25.0%) (23.9%) (27.3%) (25.6%) (11.7%) (11.8%) (31.8%) (33.2%) Other current operating income/expenses 39 28 57 33 2 (1) 1 (1) (21) (3) Share of profit/loss of associates* and joint ventures 43 38 22 3 21 36 - (1) - - Net income attributable to non-controlling interests (31) (36) (31) (37) - 1 - - - - Business operating income 2,716 2,484 9.3% 2,050 1,892 8.4% 563 478 17.8% 124 117 6.0% (21) (3) As % of net sales 30.9% 29.5% 30.1% 28.3% 38.8% 36.8% 24.1% 25.5% Financial income and expenses (139) (123) Income tax expense (642) (566) Tax rate** 25.0% 24.0% Business net income 1,935 1,795 7.8% As % of net sales 22.0% 21.3% Business earnings per share*** (in euros) 1.47 1.36 8.1% * Net of tax. ** Determined on the basis of Business income before tax, associates and non-controlling interests. *** Based on an average number of shares outstanding of 1,313.0 million in the third quarter of 2014 and 1,323.5 million in the third quarter of 2013. (1) Including impact of transition to IFRIC 21.
  • 34. 34 Business Net Income Statement Nine months 2014 Group Total Pharmaceuticals Vaccines Animal Health Others € million 9M 2014 9M 2013(1) Change 9M 2014 9M 2013(1) Change 9M 2014 9M 2013(1) Change 9M 2014 9M 2013(1) Change 9M 2014 9M 2013(1) Net sales 24,698 24,494 0.8% 20,332 20,196 0.7% 2,797 2,757 1.5% 1,569 1,541 1.8% - - Other revenues 241 267 (9.7%) 195 224 (12.9%) 23 21 9.5% 23 22 4.5% - - Cost of sales (7,988) (8,085) (1.2%) (6,082) (6,307) (3.6%) (1,329) (1,275) 4.2% (577) (503) 14.7% - - As % of net sales (32.4%) (33.0%) (29.9%) (31.2%) (47.5%) (46.3%) (36.8%) (32.6%) Gross profit 16,951 16,676 1.6% 14,445 14,113 2.4% 1,491 1,503 (0.8%) 1,015 1,060 (4.2%) - - As % of net sales 68.6% 68.1% 71.0% 69.9% 53.3% 54.5% 64.7% 68.8% Research and development expenses (3,473) (3,524) (1.4%) (3,012) (3,019) (0.2%) (351) (382) (8.1%) (110) (123) (10.6%) - - As % of net sales (14.1%) (14.4%) (14.8%) (14.9%) (12.5%) (13.9%) (7.0%) (8.0%) Selling and general expenses (6,526) (6,458) 1.1% (5,580) (5,507) 1.3% (441) (455) (3.1%) (505) (496) 1.8% - - As % of net sales (26.4%) (26.4%) (27.4%) (27.3%) (15.8%) (16.5%) (32.2%) (32.2%) Other current operating income/expenses 68 198 76 163 3 6 18 (2) (29) 31 Share of profit/loss of associates* and joint ventures 82 59 55 30 27 32 - (3) - - Net income attributable to non-controlling interests (96) (122) (96) (123) - 1 - - - - Business operating income 7,006 6,829 2.6% 5,888 5,657 4.1% 729 705 3.4% 418 436 (4.1%) (29) 31 As % of net sales 28.4% 27.9% 29.0% 28.0% 26.1% 25.6% 26.6% 28.3% Financial income and expenses (309) (400) Income tax expense (1,678) (1,557) Tax rate** 25.0% 24.0% Business net income 5,019 4,872 3.0% As % of net sales 20.3% 19.9% Business earnings per share*** (in euros) 3.81 3.68 3.5% * Net of tax. ** Determined on the basis of Business income before tax, associates and non-controlling interests. *** Based on an average number of shares outstanding of 1,315.8 million in the first nine months of 2014 and 1,323.8 million in the first nine months of 2013. (1) Including impact of transition to IFRIC 21
  • 35. Reconciliation of Business Net Income to Consolidated Net Income Attributable to Equity Holders of Sanofi 35 € million Q3 2014 Q3 2013(1) Change Business net income 1,935 1,795 7.8% Amortization of intangible assets(2) (561) (689) Impairment of intangible assets (35) (28) Fair value remeasurement of contingent consideration liabilities (45) (68) Expenses arising from the impact of acquisitions on inventories - (1) Restructuring costs (163) (71) Additional year expense related to US Branded Prescription Drug Fee(3) (116) - Tax effect of items listed above: 261 289 Amortization of intangible assets 188 233 Impairment of intangible assets 13 9 Fair value remeasurement of contingent consideration liabilities 5 23 Expenses arising from the impact of acquisitions on inventories - - Restructuring costs 55 24 Other tax items - - Share of items listed above attributable to non-controlling interests - 1 Restructuring costs of associates and joint ventures, and expenses arising from the impact of acquisitions on associates and joint ventures (86) (9) Net income attributable to equity holders of Sanofi 1,190 1,219 (2.4%) Consolidated earnings per share(4) (in euros) 0.91 0.92 (1) Including impact of transition to IFRIC 21 (2) Of which related to amortization expense generated by the remeasurement of intangible assets as part of business combinations: €540 million in the third quarter of 2014 and €658 million in the third quarter of 2013. (3) Annual fee related to 2013 sales in the U.S. following the final IRS regulation issued in July 2014 that has changed the timing of liability recognition and leads to a one-time “double” expense in the year of 2014. (4) Based on an average number of shares outstanding of 1,313.0 million in the third quarter of 2014 and 1,323.5 in the third quarter of 2013.
  • 36. Reconciliation of Business Net Income to Consolidated Net Income Attributable to Equity Holders of Sanofi 36 (1) Including impact of transition to IFRIC 21. (2) Of which related to amortization expense generated by the remeasurement of intangible assets as part of business combinations: €1,798 million in the first nine months of 2014 and €2,147 million in the first nine months of 2013. (3) Day one profit on Alnylam shares presented in financial result. (4) Annual fee related to 2013 sales following the final IRS regulation issued in July 2014 that has changed the timing of liability recognition and leads to a one-time “double” expense in the year of 2014. (5) Tax on dividends paid to shareholders of Sanofi. (6) Based on an average number of shares outstanding of 1,315.8 million in the first nine months of 2014 and 1,323.8 million in the first nine months of 2013. € million 9M 2014 9M 2013(1) Change Business net income 5,019 4,872 3.0% Amortization of intangible assets(2) (1,862) (2,232) Impairment of intangible assets (109) (468) Fair value remeasurement of contingent consideration liabilities (177) (185) Expenses arising from the impact of acquisitions on inventories - (7) Restructuring costs (298) (230) Other gains and losses, and litigation(3) 35 - Additional year expense related to US Branded Prescription Drug Fee(4) (116) - Tax effect of items listed above: 783 1,038 Amortization of intangible assets 639 723 Impairment of intangible assets 39 189 Fair value remeasurement of contingent consideration liabilities 19 43 Expenses arising from the impact of acquisitions on inventories - 2 Other gains and losses, and litigation (13) - Restructuring costs 99 81 Other tax items(5) (110) (109) Share of items listed above attributable to non-controlling interests 4 3 Restructuring costs of associates and joint ventures. and expenses arising from the impact of acquisitions on associates and joint ventures (118) (26) Net income attributable to equity holders of Sanofi 3,051 2,656 14.9% Consolidated earnings per share(6) (in euros) 2.32 2.01
  • 37. 37 Consolidated Income Statements € million Q3 2014 Q3 2013(1) 9M 2014 9M 2013(1) Net sales 8,781 8,432 24,698 24,494 Other revenues 87 86 241 267 Cost of sales (2,864) (2,871) (7,988) (8,092) Gross profit 6,004 5,647 16,951 16,669 Research and development expenses (1,146) (1,182) (3,473) (3,524) Selling and general expenses (2,309) (2,012) (6,642) (6,458) Other operating income 47 56 163 403 Other operating expenses (8) (28) (95) (205) Amortization of intangible assets (561) (689) (1,862) (2,232) Impairment of intangible assets (35) (28) (109) (468) Fair value remeasurement of contingent consideration liabilities (45) (68) (177) (185) Restructuring costs (163) (71) (298) (230) Operating income 1,784 1,625 4,458 3,770 Financial expenses (154) (147) (446) (458) Financial income 15 24 172 58 Income before tax and associates and joint ventures 1,645 1,502 4,184 3,370 Income tax expense(2) (381) (277) (1,005) (628) Share of profit/loss of associates and joint ventures (43) 29 (36) 33 Net income 1,221 1,254 3,143 2,775 Net income attributable to non-controlling interests 31 35 92 119 Net income attributable to equity holders of Sanofi 1,190 1,219 3,051 2,656 Average number of shares outstanding (million) 1,313.0 1,323.5 1,315.8 1,323.8 Earnings per share (in euros) 0.91 0.92 2.32 2.01 (1) Including impact of transition to IFRIC 21. (2) In 2014, including a tax on dividends paid to shareholders of Sanofi: (110) M€ compared to (109) M€ in 2013.
  • 38. Business EPS Currency Sensitivity € 23.1% US $ 37.3% Japanese Yen 5.5% £ 2.2% Australian $ 1.6% Canadian $ 1.5% Brazilian Real 3.5% Chinese Yuan 4.3% Russian Ruble 2.2% Others 16.8% Mexican Peso 2.0% Currency Exposure on Q3 2014 Sales Currency Average Rates 2014 Currency Sensitivity 38 ● 1% variation in €/$ corresponds to an impact of 0.5% on 2014 Business EPS ●1% variation in €/Yen corresponds to an impact of 0.1% on 2014 Business EPS Q3 2013 Q3 2014 % change €/$ 1.32 1.33 +0.8% €/Yen 131.05 137.74 +5.1% €/Real 3.03 3.01 -0.7% €/Ruble 43.45 48.08 +10.7%