Gilead Sciences Announces Second Quarter 2015 Financial Results

- Over 180,000 U.S. and EU Patients Treated Year-to-Date with Sovaldi or Harvoni -

- Product Sales of $8.1 billion -

- Non-GAAP EPS of $3.15 per share -

- Revised 2015 Full Year Guidance -

FOSTER CITY, Calif.--(BUSINESS WIRE)--Jul. 28, 2015-- Gilead Sciences, Inc. (Nasdaq: GILD) announced today its results of operations for the second quarter ended June 30, 2015. The financial results that follow represent a year over year comparison of second quarter 2015 to the second quarter 2014. Total revenues were $8.2 billion in 2015 compared to $6.5 billion in 2014. Net income was $4.5 billion or $2.92 per diluted share in 2015 compared to $3.7 billion or $2.20 per diluted share in 2014. Non-GAAP net income, which excludes amounts related to acquisition, restructuring, stock-based compensation and other, was $4.8 billion or $3.15 per diluted share in 2015 compared to $3.9 billion or $2.36 per diluted share in 2014.

  Three Months Ended   Six Months Ended
June 30, June 30,
(In millions, except per share amounts) 2015   2014 2015   2014
Product sales $ 8,126 $ 6,413 $ 15,531 $ 11,284
Royalty, contract and other revenues 118   122   307   250
Total revenues $ 8,244   $ 6,535   $ 15,838   $ 11,534
 
Net income attributable to Gilead $ 4,492 $ 3,656 $ 8,825 $ 5,883
Non-GAAP net income attributable to Gilead $ 4,845 $ 3,929 $ 9,449 $ 6,417
 
Diluted EPS $ 2.92 $ 2.20 $ 5.68 $ 3.52
Non-GAAP diluted EPS $ 3.15 $ 2.36 $ 6.08 $ 3.84
 

Product Sales

Total product sales for the second quarter of 2015 were $8.1 billion compared to $6.4 billion for the second quarter of 2014. Product sales in the U.S. were $5.6 billion compared to $4.8 billion for the second quarter of 2014. In Europe, product sales were $2.0 billion compared to $1.3 billion for the same period in 2014.

Antiviral Product Sales

Antiviral product sales increased to $7.6 billion for the second quarter of 2015, up from $6.0 billion for the second quarter of 2014 primarily due to sales of Harvoni® (ledipasvir 90 mg/sofosbuvir 400 mg), which was approved in the U.S. and Europe in the fourth quarter of 2014, partially offset by a decrease in sales of Sovaldi® (sofosbuvir 400 mg) due primarily to the uptake in Harvoni.

Other Product Sales

Other product sales, which include Letairis® (ambrisentan), Ranexa® (ranolazine) and AmBisome® (amphotericin B liposome for injection), were $495 million for the second quarter of 2015 compared to $401 million for the second quarter of 2014.

Operating Expenses

  Three Months Ended   Six Months Ended
June 30, June 30,
(In millions) 2015   2014 2015   2014
Non-GAAP research and development expenses $ 702 $ 542 $ 1,353 $ 1,100
Non-GAAP selling, general and administrative expenses $ 761 $ 570 $ 1,361 $ 1,070

Note: Non-GAAP R&D and SG&A expenses exclude amounts related to acquisition, restructuring, stock-based compensation and other.

During the second quarter of 2015, compared to the same period in 2014:

  • Non-GAAP research and development (R&D) expenses increased primarily due to the continued progression and expansion of Gilead's clinical studies, particularly Phase 3 studies in the liver disease and oncology areas.
  • Non-GAAP selling, general and administrative (SG&A) expenses increased primarily due to an increase in Gilead's portion of the branded prescription drug fee along with growth and the geographic expansion in its business.

Cash, Cash Equivalents and Marketable Securities

As of June 30, 2015, Gilead had $14.7 billion of cash, cash equivalents and marketable securities compared to $14.5 billion as of March 31, 2015. During the second quarter of 2015, Gilead generated $5.7 billion in operating cash flow, utilized $900 million to repurchase 9 million shares under the $15.0 billion share repurchase plan approved in January 2015 and $3.9 billion to retire 46 million warrants related to the 2016 convertible debt. At June 30, 2015, approximately 9 million warrants remain outstanding. Gilead also paid its first cash dividend of $633 million, or $0.43 per share, during the second quarter of 2015.

Revised 2015 Full Year Guidance

Gilead updated its full year 2015 guidance, which it initially provided on February 3, 2015, updated on April 30, 2015, and further revised on July 28, 2015.

(In millions, except percentages and per share amounts)   Initially Provided

February 3, 2015

    Updated

April 30, 2015

    Updated

July 28, 2015

Net Product Sales $26,000 - $27,000     $28,000 - $29,000     $29,000 - $30,000
Non-GAAP*
Product Gross Margin 87% - 90% 87% - 90% 88% - 90%
R&D expenses $3,000 - $3,300 $3,000 - $3,300 $2,800 - $3,000
SG&A expenses $3,000 - $3,300 $3,000 - $3,300 $3,000 - $3,200
Effective Tax Rate 18.0% - 20.0% 18.0% - 20.0% 17.0% - 18.0%
 
Diluted EPS Impact of Acquisition-Related, Restructuring, Stock-Based Compensation Expenses and Other $0.82 - $0.87 $0.82 - $0.87 $0.82 - $0.87
 
* Non-GAAP product gross margin, R&D and SG&A expenses and effective tax rate exclude amounts related to acquisition, restructuring, stock-based compensation and other.

Corporate Highlights

  • Announced the signing of a definitive agreement to acquire EpiTherapeutics, a privately-held Danish company. EpiTherapeutics generated a library of first-in-class, selective small molecule inhibitors of epigenetic regulation of gene transcription, in particular histone demethylases.
  • Announced that the company’s Board of Directors declared a quarterly cash dividend of $633 million or $0.43 per share of common stock and paid on June 29, 2015 to all stockholders of record as of the close of business on the record date of June 16, 2015. This was the first quarterly dividend declared under the Board's dividend program announced on February 3, 2015.

Product & Pipeline Updates Announced by Gilead During the Second Quarter of 2015 Include:

Antiviral Program

  • Announced that Gilead submitted a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for two doses of an investigational fixed-dose combination of emtricitabine and tenofovir alafenamide (F/TAF) (200/10 mg and 200/25 mg) for the treatment of HIV-1 infection in adults and pediatric patients age 12 years and older, in combination with other HIV antiretroviral agents. Under the Prescription Drug User Fee Act, the FDA has set a target action date of April 7, 2016.
    • This was Gilead's second F/TAF-based NDA submitted to the FDA for review. In November 2014, Gilead filed an NDA for an investigational once-daily single tablet regimen containing elvitegravir 150 mg, cobicistat 150 mg, emtricitabine 200 mg and TAF 10 mg (E/C/F/TAF). The FDA has set a target action date of November 5, 2015.
  • Announced that Gilead’s Marketing Authorization Application (MAA) for two doses of F/TAF (200/10 mg and 200/25 mg) was fully validated and under evaluation by the European Medicines Agency. The data included in the application support the use of F/TAF for the treatment of HIV-1 infection in adults in combination with other HIV antiretroviral agents.
    • Gilead's MAA for E/C/F/TAF was validated on December 23, 2014.
  • Presented data at the 50th Annual Meeting of the European Association for the Study of the Liver including:
    • Positive results from two studies evaluating the safety and efficacy of investigational uses of sofosbuvir-based regimens in HCV-infected patients with genotypes 2, 3, 4 and 5. Results from the BOSON study of sofosbuvir in combination with ribavirin or with pegylated interferon and ribavirin demonstrated high cure rates across all patients with genotypes 2 and 3. Separately, results from a Phase 2 study demonstrated the safety and efficacy of ledipasvir/sofosbuvir in patients with genotypes 4 or 5 infection.
    • Positive results from several Phase 2 clinical studies evaluating investigational uses of ledipasvir/sofosbuvir and other sofosbuvir-based regimens for the treatment of HCV infection in patients with advanced liver disease, including patients with decompensated cirrhosis, patients with fibrosing cholestatic hepatitis C (a rare and severe form of the disease following liver transplantation) and patients with portal hypertension.
    • Positive pre-clinical data and results from Phase 1 and Phase 2 studies supporting the development of an investigational all-oral, pan-genotypic regimen of sofosbuvir, the investigational NS5A inhibitor velpatasvir (formerly GS-5816) and GS-9857, an investigational NS3/4A protease inhibitor. In pre-clinical studies, GS-9857 demonstrated similarly potent antiviral activity against HCV replicons of all tested genotypes (1-6), as well as an improved resistance profile compared to other HCV protease inhibitors. In a healthy volunteer study, GS-9857 demonstrated a favorable pharmacokinetic profile. Data from a three-day monotherapy study also demonstrated that GS-9857 was well-tolerated for HCV patients with genotypes 1, 2, 3 and 4 at the 100 mg dose.

Oncology Program

  • Announced positive results from the Phase 3 clinical Study 119 of an investigational use of Zydelig® (idelalisib) in combination with ofatumumab in previously-treated patients with chronic lymphocytic leukemia. In Study 119, there was a 73-percent reduction in the risk of disease progression or death in patients receiving Zydelig in combination with ofatumumab compared to ofatumumab alone. These results were presented at the 51st Annual Meeting of the American Society of Clinical Oncology.

Conference Call

At 4:30 p.m. Eastern Time today, Gilead's management will host a conference call and a simultaneous webcast to discuss results from its second quarter 2015 as well as provide a general business update. The live webcast of the call can be accessed at the company's Investors page at www.gilead.com/investors. Please connect to the company's website at least 15 minutes prior to the start of the call to ensure adequate time for any software download that may be required to listen to the webcast. Alternatively, please call 1-877-359-9508 (U.S.) or 1-224-357-2393 (international) and dial the conference ID 73361664 to access the call.

A replay of the webcast will be archived on the company's website for one year, and a phone replay will be available approximately two hours following the call through July 30, 2015. To access the phone replay, please call 1-855-859-2056 (U.S.) or 1-404-537-3406 (international) and dial the conference ID 73361664.

About Gilead

Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases. Gilead has operations in more than 30 countries worldwide, with headquarters in Foster City, California.

Non-GAAP Financial Information

Gilead has presented certain financial information in accordance with U.S. generally accepted accounting principles (GAAP) and also on a non-GAAP basis. Management believes this non-GAAP information is useful for investors, when considered in conjunction with Gilead's GAAP financial statements, because management uses such information internally for its operating, budgeting and financial planning purposes. Non-GAAP information is not prepared under a comprehensive set of accounting rules and should only be used to supplement an understanding of Gilead's operating results as reported under GAAP. A reconciliation between GAAP and non-GAAP financial information is provided in the tables on pages 7 and 8.

Forward-looking Statements

Statements included in this press release that are not historical in nature are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Gilead cautions readers that forward-looking statements are subject to certain risks and uncertainties that could cause actual results to differ materially. These risks and uncertainties include: Gilead's ability to achieve its anticipated full year 2015 financial results; Gilead's ability to sustain growth in revenues for its antiviral and other programs; availability of funding for state AIDS Drug Assistance Programs (ADAPs); continued fluctuations in ADAP purchases driven by federal and state grant cycles which may not mirror patient demand and may cause fluctuations in Gilead's earnings; the possibility of unfavorable results from clinical trials involving sofosbuvir-containing products, including the pan-genotypic regimen of sofosbuvir, velpatasvir and GS-9857; Gilead's ability to initiate clinical trials in its currently anticipated timeframes; the levels of inventory held by wholesalers and retailers which may cause fluctuations in Gilead's earnings; Gilead's ability to submit new drug applications for new product candidates in the timelines currently anticipated; Gilead's ability to receive regulatory approvals in a timely manner or at all, for new and current products, including F/TAF and E/C/F/TAF; Gilead's ability to successfully commercialize its products; the risk that physicians and patients may not see advantages of these products over other therapies and may therefore be reluctant to prescribe the products; the risk that estimates of patients with HCV or anticipated patient demand may not be accurate; the risk that private and public payers may be reluctant to provide, or continue to provide, coverage or reimbursement for new products, including Sovaldi and Harvoni; Gilead's ability to successfully develop its oncology, inflammation, cardiovascular and respiratory programs, including the compounds purchased from EpiTherapeutics; safety and efficacy data from clinical studies may not warrant further development of Gilead's product candidates, including the pan-genotypic regimen of sofosbuvir, velpatasvir and GS-9857; the potential for additional austerity measures in European countries that may increase the amount of discount required on Gilead's products; Gilead's ability to complete its share repurchase program due to changes in its stock price, corporate or other market conditions; Gilead’s ability to pay dividends under its dividend program and the risk that its Board of Directors may reduce the amount of the dividend; fluctuations in the foreign exchange rate of the U.S. dollar that may cause an unfavorable foreign currency exchange impact on Gilead's future revenues and pre-tax earnings; and other risks identified from time to time in Gilead's reports filed with the U.S. Securities and Exchange Commission (SEC). In addition, Gilead makes estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses and related disclosures. Gilead bases its estimates on historical experience and on various other market specific and other relevant assumptions that it believes to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ significantly from these estimates. You are urged to consider statements that include the words may, will, would, could, should, might, believes, estimates, projects, potential, expects, plans, anticipates, intends, continues, forecast, designed, goal, or the negative of those words or other comparable words to be uncertain and forward-looking. Gilead directs readers to its press releases, Quarterly Report on Form 10-Q for the quarter ended March 31, 2015 and other subsequent disclosure documents filed with the SEC. Gilead claims the protection of the Safe Harbor contained in the Private Securities Litigation Reform Act of 1995 for forward-looking statements.

All forward-looking statements are based on information currently available to Gilead, and Gilead assumes no obligation to update any such forward-looking statements.

Gilead owns or has rights to various trademarks, copyrights and trade names used in our business, including the following: GILEAD®, GILEAD SCIENCES®, HARVONI®, SOVALDI®, TRUVADA®, STRIBILD®, COMPLERA®, EVIPLERA®, VIREAD®, LETAIRIS®, RANEXA®, AMBISOME®, ZYDELIG®, EMTRIVA®, TYBOST®, HEPSERA®, VITEKTA®, CAYSTON®, VOLIBRIS®, and RAPISCAN®.

ATRIPLA® is a registered trademark belonging to Bristol-Myers Squibb & Gilead Sciences, LLC. LEXISCAN® is a registered trademark belonging to Astellas U.S. LLC. MACUGEN® is a registered trademark belonging to Eyetech, Inc. SUSTIVA® is a registered trademark of Bristol-Myers Squibb Pharma Company. TAMIFLU® is a registered trademark belonging to Hoffmann-La Roche Inc.

For more information on Gilead Sciences, Inc., please visit www.gilead.com or call the Gilead Public Affairs Department at 1-800-GILEAD-5 (1-800-445-3235).

 

GILEAD SCIENCES, INC.

CONDENSED CONSOLIDATED STATEMENTS OF INCOME

(unaudited)

(in millions, except per share amounts)

   
Three Months Ended Six Months Ended
June 30, June 30,
2015   2014 2015   2014
Revenues:
Product sales $ 8,126 $ 6,413 $ 15,531 $ 11,284
Royalty, contract and other revenues 118   122   307   250  
Total revenues 8,244   6,535   15,838   11,534  
Costs and expenses:
Cost of goods sold 998 925 1,880 1,738
Research and development expenses 818 584 1,514 1,179
Selling, general and administrative expenses 812   614   1,457   1,162  
Total costs and expenses 2,628   2,123   4,851   4,079  
Income from operations 5,616 4,412 10,987 7,455
Interest expense (140 ) (102 ) (293 ) (178 )
Other income (expense), net 35   (4 ) 56   (22 )
Income before provision for income taxes 5,511 4,306 10,750 7,255
Provision for income taxes 1,014   656   1,921   1,382  
Net income 4,497 3,650 8,829 5,873
Net income (loss) attributable to noncontrolling interest 5   (6 ) 4   (10 )
Net income attributable to Gilead $ 4,492   $ 3,656   $ 8,825   $ 5,883  
Net income per share attributable to Gilead common stockholders - basic $ 3.05 $ 2.39 $ 5.96 $ 3.83
Net income per share attributable to Gilead common stockholders - diluted $ 2.92 $ 2.20 $ 5.68 $ 3.52
Shares used in per share calculation - basic 1,472 1,533 1,480 1,535
Shares used in per share calculation - diluted 1,540 1,664 1,555 1,672
Cash dividends declared per share $ 0.43 $ $ 0.43 $
 

GILEAD SCIENCES, INC.

RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION

(unaudited)

(in millions, except percentages and per share amounts)

   
Three Months Ended Six Months Ended
June 30, June 30,
2015   2014 2015   2014
Cost of goods sold reconciliation:
GAAP cost of goods sold $ 998 $ 925 $ 1,880 $ 1,738
Stock-based compensation expenses (3 ) (2 ) (6 ) (5 )
Acquisition related-amortization of purchased intangibles (207 ) (200 ) (413 ) (399 )
Variable interest entity consolidated costs(1)     1    
Non-GAAP cost of goods sold $ 788   $ 723   $ 1,462   $ 1,334  
 
Product gross margin reconciliation:
GAAP product gross margin 87.7 % 85.6 % 87.9 % 84.6 %
Acquisition related-amortization of purchased intangibles 2.5 % 3.1 % 2.7 % 3.5 %
Non-GAAP product gross margin(2) 90.3 % 88.7 % 90.6 % 88.2 %
 
Research and development expenses reconciliation:
GAAP research and development expenses $ 818 $ 584 $ 1,514 $ 1,179
Stock-based compensation expenses (42 ) (37 ) (84 ) (71 )
Acquisition related expenses (67 ) (67 )
Acquisition related-contingent consideration remeasurement (7 ) (5 ) (10 ) (8 )
Non-GAAP research and development expenses $ 702   $ 542   $ 1,353   $ 1,100  
 
Selling, general and administrative expenses reconciliation:
GAAP selling, general and administrative expenses $ 812 $ 614 $ 1,457 $ 1,162
Stock-based compensation expenses (51 ) (44 ) (98 ) (90 )
Restructuring expenses 2
Acquisition related-amortization of purchased intangibles       (2 )
Non-GAAP selling, general and administrative expenses $ 761   $ 570   $ 1,361   $ 1,070  
 
Operating margin reconciliation:
GAAP operating margin 68.1 % 67.5 % 69.4 % 64.6 %
Stock-based compensation expenses 1.2 % 1.3 % 1.2 % 1.4 %
Acquisition related expenses 0.8 % % 0.4 % %
Acquisition related-amortization of purchased intangibles 2.5 % 3.1 % 2.6 % 3.5 %
Acquisition related-contingent consideration remeasurement 0.1 % 0.1 % 0.1 % 0.1 %
Non-GAAP operating margin(2) 72.7 % 71.9 % 73.6 % 69.6 %
 
Other income (expense) reconciliation:
GAAP other income (expense), net $ 35 $ (4 ) $ 56 $ (22 )
Acquisition related-transaction costs       (2 )
Non-GAAP other income (expense), net $ 35   $ (4 ) $ 56   $ (24 )
 
Notes:
Immaterial amounts are not presented in the tables above
(1) Consolidation of a contract manufacturer

(2) Amounts may not sum due to rounding

 

GILEAD SCIENCES, INC.

RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION - (Continued)

(unaudited)

(in millions, except percentages and per share amounts)

   
Three Months Ended Six Months Ended
June 30, June 30,
2015   2014 2015   2014
Effective tax rate reconciliation:
GAAP effective tax rate 18.4 % 15.2 % 17.9 % 19.1 %
Acquisition related expenses/transaction costs (0.2 )% % (0.1 )% %
Acquisition related-amortization of purchased intangibles (0.5 )% (0.6 )% (0.5 )% (0.9 )%
Non-GAAP effective tax rate(1) 17.7 % 14.6 % 17.3 % 18.2 %
 
Net income attributable to Gilead reconciliation:
GAAP net income attributable to Gilead $ 4,492 $ 3,656 $ 8,825 $ 5,883
Stock-based compensation expenses 71 72 140 136
Restructuring expenses (2 )
Acquisition related expenses/transaction costs 67 67 (1 )
Acquisition related-amortization of purchased intangibles 202 196 403 391
Acquisition related-contingent consideration remeasurement 7 5 10 8
Variable interest entity consolidated costs(2) 6     6    
Non-GAAP net income attributable to Gilead $ 4,845   $ 3,929   $ 9,449   $ 6,417  
 
Diluted earnings per share reconciliation:
GAAP diluted earnings per share $ 2.92 $ 2.20 $ 5.68 $ 3.52
Stock-based compensation expenses 0.05 0.04 0.09 0.08
Acquisition related expenses/transaction costs 0.04 0.04
Acquisition related-amortization of purchased intangibles 0.13 0.12 0.26 0.23
Acquisition related-contingent consideration remeasurement     0.01    
Non-GAAP diluted earnings per share(1) $ 3.15   $ 2.36   $ 6.08   $ 3.84  
 
Shares used in per share calculation (diluted) reconciliation:
GAAP shares used in per share calculation (diluted) 1,540 1,664 1,555 1,672
Share impact of current stock-based compensation rules   (1 )   (1 )
Non-GAAP shares used in per share calculation (diluted) 1,540   1,663   1,555   1,671  
 
Non-GAAP adjustment summary:
Cost of goods sold adjustments $ 210 $ 202 $ 418 $ 404
Research and development expenses adjustments 116 42 161 79
Selling, general and administrative expenses adjustments 51 44 96 92
Other income (expense) adjustments       (2 )
Total non-GAAP adjustments before tax 377 288 675 573
Income tax effect (30 ) (14 ) (58 ) (38 )
Variable interest entity consolidated costs(2) 6     7    
Total non-GAAP adjustments after tax attributable to Gilead $ 353   $ 274   $ 624   $ 535  
 
Notes:
Immaterial amounts are not presented in the tables above
(1) Amounts may not sum due to rounding
(2) Consolidation of a contract manufacturer
 

GILEAD SCIENCES, INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

(unaudited)

(in millions)

   

    June 30,    

December 31,
2015 2014(1)
 
Cash, cash equivalents and marketable securities $ 14,667 $ 11,726
Accounts receivable, net 5,331 4,635
Inventories 2,039 1,386
Property, plant and equipment, net 1,899 1,674
Intangible assets, net 10,660 11,073
Goodwill 1,172 1,172
Other assets 3,399   2,998
Total assets $ 39,167   $ 34,664
 
Current liabilities $ 8,925 $ 5,761
Long-term liabilities 13,601 13,069
Equity component of currently redeemable convertible notes 7 15
Stockholders’ equity(2) 16,634   15,819
Total liabilities and stockholders’ equity $ 39,167   $ 34,664
 
Notes:

(1) Derived from the audited consolidated financial statements as of December 31, 2014.

(2) As of June 30, 2015, there were 1,473 million shares of common stock issued and outstanding.

 

GILEAD SCIENCES, INC.

PRODUCT SALES SUMMARY

(unaudited)

(in millions)

   
Three Months Ended Six Months Ended
June 30, June 30,
2015   2014 2015   2014
Antiviral products:
Harvoni – U.S. $ 2,826 $ $ 5,842 $
Harvoni – Europe 623 1,100
Harvoni – Other International 159     245  
3,608     7,187  
 
Sovaldi – U.S. 615 3,031 1,036 5,129
Sovaldi – Europe 522 401 1,005 564
Sovaldi – Other International 154   49   222   62
1,291   3,481   2,263   5,755
 
Truvada – U.S. 500 399 909 767
Truvada – Europe 277 338 578 661
Truvada – Other International 72   69   133   138
849   806   1,620   1,566
 
Atripla – U.S. 549 578 1,043 1,068
Atripla – Europe 178 234 372 471
Atripla – Other International 55   58   101   111
782   870   1,516   1,650
 
Stribild – U.S. 364 230 646 417
Stribild – Europe 65 31 126 55
Stribild – Other International 18   9   31   13
447   270   803   485
 
Complera / Eviplera – U.S. 207 153 370 284
Complera / Eviplera – Europe 145 132 290 241
Complera / Eviplera – Other International 15   14   27   25
367   299   687   550
 
Viread – U.S. 134 117 234 198
Viread – Europe 77 88 157 172
Viread – Other International 60   56   114   102
271   261   505   472
 
Other Antiviral – U.S. 8 13 22 20
Other Antiviral – Europe 7 10 14 19
Other Antiviral – Other International 1   2   2   4
16   25   38   43
 
Total antiviral products – U.S. 5,203 4,521 10,102 7,883
Total antiviral products – Europe 1,894 1,234 3,642 2,183
Total antiviral products – Other International 534   257   875   455
7,631   6,012   14,619   10,521
Other products:
Letairis 176 145 327 268
Ranexa 141 123 258 234
AmBisome 103 94 188 186
Zydelig 30 56
Other 45   39   83   75
495   401   912   763
 
Total product sales $ 8,126   $ 6,413   $ 15,531   $ 11,284

Source: Gilead Sciences, Inc.

Gilead Sciences, Inc.
Robin Washington, 650-522-5688 (Investors)
Patrick O'Brien, 650-522-1936 (Investors)
Amy Flood, 650-522-5643 (Media)