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Teva Pharmaceutical Industries Ltd.

Quarterly Report Jan 29, 2025

7082_rns_2025-01-29_b2607415-025b-48bb-91b9-62cf29dc23b4.pdf

Quarterly Report

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UNITED STATES SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 8-K

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Date of Report (Date of earliest event reported) January 29, 2025

TEVA PHARMACEUTICAL INDUSTRIES LIMITED

(Exact name of registrant as specified in its charter)

Israel 001-16174 00-0000000 (State or Other Jurisdiction (Commission (IRS Employer of Incorporation) File Number) Identification No.)

124 Dvora Hanevi'a Street Tel Aviv 6944020, Israel (Address of Principal Executive Offices, including Zip Code)

+972-3-914-8213

(Registrant's Telephone Number, including Area Code)

Not Applicable

(Former Name or Former Address, if Changed Since Last Report)

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

☐ Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

☐ Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

☐ Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

☐ Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:
Title of each class Trading
Symbol(s)
Name of each exchange on which registered
American Depositary Shares, each
representing one Ordinary Share
TEVA New York Stock Exchange

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging Growth Company ☐

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

ITEM 2.02 Results of Operations and Financial Condition

On January 29, 2025, Teva Pharmaceutical Industries Ltd. issued a press release announcing its financial results for the period ended December 31, 2024. A copy of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K and the information contained therein is incorporated herein by reference.

The information included in this Item 2.02 is being furnished to the Securities and Exchange Commission and shall not be deemed "filed" for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the "Exchange Act"), nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.

ITEM 9.01 Financial Statements and Exhibits

(d) Exhibits

Exhibit No. Description of Document 99.1 Teva Reports 2024 Full Year and Fourth Quarter Financial Results

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

TEVA PHARMACEUTICAL INDUSTRIES LIMITED

Date: January 29, 2024 By:/s/ Eli Kalif

Name:Eli Kalif Title: Executive Vice President, Chief Financial Officer

04 2024 FY 2024
Revenues \$4.2 billion \$16.5 billion
GAAP loss per share 50.19 51.45
Non-GAAP diluted EPS \$0.71 52.49
Cash flow generated from
operating activities
\$575 million \$1,247 million
Free cash flow \$790 million \$2,068 million

Teva Media Inquiries [email protected]

  • o Revenues of \$16.8 \$17.4 billion
  • Non-GAAP operating income of \$4.1-\$4.6 billion
  • o Adjusted EBITDA of \$4.5 \$5.0 billion
  • o Non-GAAP diluted EPS of \$2.35 \$2.65
  • o Free cash flow of \$1.6 \$1.9 billion

* 2025 outlook assumes a full year contribution from Teva api and our business venture in Japan and excludes the expected income from potential milestone payments from Sanofi in connection with the Phase 3 initiation of duvakitug.

Tel Aviv, Israel, January 29, 2025 - Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today reported results for the year and the quarter ended December 31, 2024.

Mr. Richard Francis, Teva's President and CEO, said: "2024 marked a transformative year for Teva, resulting in a second consecutive year of growth, driven by our generic products and key innovative products. Focusing on rigorous execution of our Pivot to Growth strategy throughout the year, we continued to achieve important milestones in each of its four pillars, including surpassing the outlook for our key innovative products, growing our generics business across all segments, and accelerating our early-stage innovative pipeline, including the positive Phase 2b results for our duvakitug (anti-Tl1A) asset. These results pave the way for pivotal trials in Crohn's disease and ulcerative colitis, as well as, potentially, other Immunological and fibrotic indications beyond, in collaboration with our partner, Sanofi.

Mr. Francis continued, "In 2025, we anticipate further progress in our key innovative growth drivers, while also executing on our complex generics and biosimilars business, supported by new product launches. We are also excited to advance to Phase 3 trials for our duvakitug (anti-TL1A) asset."

Pivot to Growth Strategy

In 2024, we continued to execute on the four key pillars of our "Pivot to Growth" strategy, which we announced in May 2023.

  • · On the first pillar, delivering on our growth engines, we continued to show strong performance of our key innovative products, mainly AUSTEDO, AJOVY, and UZEDY, as well as on our late-stage pipeline of biosimilars, with the launches of SIMLANDI® (adalimumab-ryvk) injection and the expected launch of SELARSDI (ustekinumab-aekn) injection, and the progress we made on our proposed biosimilars to Prolia®(denosumab), Simponi® and Simponi Aria® (golimumab), which were submitted for requlatory review in the U.S. and the EU;
  • · On the second pillar, stepping up innovation through delivering on our late-stage innovative pipeline, we have been accelerating the development of certain key pipeline assets, including the recent positive Phase 2b results for duvakituq (anti-TL1A), and expect a number of milestones and data points for olanzapine LAI, and DARI (dual-action asthma rescue inhaler, ICS/SABA) in the near future;
  • · On the third pillar, sustaining our generics powerhouse with a global commercial footprint, focused portfolio, pipeline and manufacturing footprint, we continued to optimize our generics business and build a strong pipeline of biosimilars, with several successful launches of high-value complex generics in 2024; and
  • Lastly, on our fourth pillar, focusing our business by optimizing our portfolio and global manufacturing footprint. This will enable strateqic capital deployment, to accelerate our growth

Our average debt maturity was approximately 5.5 years as of December 31, 2024, compared to 6.0 years as of December 31, 2023.

Fourth Quarter 2024 Consolidated Results

Revenues in fourth quarter of 2024 were \$4,229 million, a decrease of 5% in both U.S. dollars and in local currency terms, compared to the fourth quarter of 2023. This decrease was mainly due to an upfront payment of \$500 million received in 2023 related to the collaboration on our duvakitug (anti-TL1A) asset, partially offset by higher revenues from our innovative products AUSTEDO, UZEDY and AJOVY, from generic products in all our segments and from the sale of certain product rights.

Exchange rate movements during the fourth quarter of 2024, net of hedging effects, negatively impacted overall revenues by \$8 million, compared to the fourth quarter of 2023.

Gross profit in the fourth quarter of 2024 was \$2,120 million, a decrease of 12% compared to \$2,416 million in the fourth quarter of 2023. Gross profit margin was 50.1% in the fourth quarter of 2024, compared to 54.2% in the fourth quarter of 2023. Non-GAAP gross profit was \$2,319 million in the fourth quarter of 2024, a decrease of 11%, compared to \$2,592 million in the fourth quarter of 2023. Non-GAAP gross profit margin was 54.8% in the fourth quarter of 2024, compared to 58.2% in the fourth quarter of 2023. The decrease in both gross profit margin and non-GAAP gross profit margin was mainly due to the upfront payment received in 2023 related to the collaboration on our duvakitug (anti-TL1A) asset, as well as lower revenues from COPAXONE, partially offset by higher revenues from AUSTEDO, as well as the sale of certain product rights.

Research and Development (R&D) expenses, net in the fourth quarter of 2024 were \$248 million, an increase of 9% compared to \$227 million in the fourth quarter of 2023, as we continue to execute on our Pivot to Growth stratequ. Our higher R&D expenses, net in the fourth quarter of 2024 compared to the fourth quarter of 2023, were mainly due to an increase in our late-stage innovative pipeline in neuroscience (mainly neuropsychiatry), in immunology, and in immuno-oncology.

Selling and Marketing (S&M) expenses in the fourth quarter of 2024 were \$650 million, an increase of 7% compared to the fourth quarter of 2023. This increase was mainly to support revenue growth in our innovative portfolio, primarily AUSTEDO, generic products and AJOVY.

General and Administrative (G&A) expenses in the fourth quarter of 2024 were \$302 million, an increase of 4% compared to the fourth quarter of 2023.

Other loss (income) in the fourth quarter of 2024 was a loss of \$8 million, compared to an income of \$6 million in the fourth quarter of 2023.

Operating loss in the fourth quarter of 2024 was \$29 million, compared to an operating income of \$755 million in the fourth quarter of 2023. Operating loss as a percentage of revenues was 0.7% in the fourth quarter of 2024, compared to an operating income as a percentage of revenues of 17% in the fourth quarter of 2023. Non-GAAP operating income in the fourth quarter of 2024 was \$1,168 million representing a non-GAAP operating margin of 27.6%, compared to non-GAAP operating income of \$1,546 million representing a non-GAAP operating margin of 34.7% in the fourth quarter of 2023. The decrease in non-GAAP operating margin in the fourth quarter of 2024 was mainly due to an increase in operating expenses as a percentage of revenues, as well as due to lower non-GAAP gross profit margin, as discussed above.

Exchange rate movements during the fourth quarter of 2024, net of hedging effects, positively impacted our operating income and non-GAAP operating income by \$21 million and \$20 million, respectively, compared to the fourth quarter of 2023.

- •••••••••••

-

-

-

-

  • · Items attributable to non-controlling interests of \$63 million; and
  • · Corresponding tax effects and unusual tax items of \$114 million.

We believe that excluding such items facilitates investors' understanding of our business including underlying performance trends, thereby improving the comparability of our business performance results between reporting periods.

For a reconciliation of the U.S. GAAP results to the adjusted non-GAAP figures and for additional information, see the tables below and the information included under "Non-GAAP Financial Measures." Investors should consider non-GAAP financial measures in addition to, and not as replacement for, or superior to, measures of financial performance prepared in accordance with GAAP.

Cash flow generated from operating activities during the fourth quarter of 2024 was \$575 million, compared to \$1,184 million of cash flow generated from operating activities in the fourth quarter of 2023. The lower cash flow generated from operating activities in the fourth quarter of 2024 resulted mainly from changes in working capital items, including a negative impact of accounts payables, the classification of payments to Allergan in connection with lenalidomide (generic equivalent of Revlimid®) as cash flow used in operating activities, an upfront payment received in 2023 related to the collaboration on our duvakitug (anti-TL1A) asset, partially offset by lower legal payments during the fourth quarter of 2024, mainly in connection with our opioids litigation.

During the fourth quarter of 2024, we generated free cash flow of \$790 million, which we define as comprising \$575 million in cash flow generated from operating activities, \$340 million in beneficial interest collected in exchange for securitized accounts receivables (under our EU securitization program) and \$4 million in divestitures of businesses and other assets, partially offset by \$129 million in cash used for capital investment. During the fourth quarter of 2023, we generated free cash flow of \$1,486 million, which we define as comprising \$1,184 million in cash flow generated from operating activities, \$421 million in beneficial interest collected in exchange for securitized accounts receivables (under our EU securitization program), partially offset by \$120 million in cash used for capital investment. This decrease resulted mainly from lower cash flow generated from operating activities.

Segment Results for the Fourth Quarter of 2024

United States Segment

As part of a recent shift in executive management responsibilities and in line with our Pivot to Growth strategy, commencing January 1, 2024, Canada is reported as part of our International Markets segment. Prior period amounts were recast to reflect this change.

The following table presents revenues, expenses and profit for our United States segment for the three months ended December 31, 2024 and 2023:

Three months ended December 31
2024 2023
(U.S. \$ in millions / % of Segment Revenues)
Revenues S 1,975 100% \$ \$ 2.266 100%
Cost of sales 877 44.4% 822 36.3%
Gross profit 1.097 55.6% 1.444 63.7%
R&D expenses 158 8.0% 144 6.3%
S&M expenses 260 13.2% 238 10.5%
G&A expenses 109 5.5% 90 4.0%
Other loss (income) (1)
Segment profit* \$ 28.8% 43.0%

* Seqment profit does not include amortization and certain other items.

& Represents an amount less than 0.5%.

Revenues from our United States segment in the fourth quarter of 2024 were \$1,975 million, a decrease of \$291 million, or 13%, compared to the fourth quarter of 2023. This decrease was mainly due to an upfront payment received in 2023 related to the collaboration on our duvakitug (anti-TL1A) asset, partially offset by higher revenues from our innovative products AUSTEDO, and UZEDY, as well as the revenues from the sale of certain product rights.

Revenues by Major Products and Activities

The following table presents revenues for our United States segment by major products and activities for the three months ended December 31, 2024 and 2023:

Three months ended
December 31,
Percentage
Change
2024 2023 2024-2023
(U.S. \$ in millions)
Generic products (including biosimilars) ಲ್ಲಿ 674 ഗ് 667 1%
AJOVY 63 57 11%
AUSTEDO 518 408 27%
BENDEKA and TREANDA…………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………… 41 52 (21%)
COPAXONE 63 72 (13%)
UZEDY 43 N/A
Anda 402 394 2%
Other* 171 607 (72%)
Total \$ 1,975 2,266 (13%)

*Other revenues in the fourth quarter of 2024 include the sale of certain product rights. Other revenues in the fourth quarter of 2023 were mainly comprised of a \$500 million upfront payment received in connection with the collaboration on our duvakitug (anti-TL1A) asset.

Generic products (including biosimilars) revenues in our United States segment in the fourth quarter of 2024 were \$674 million, an increase of 1% compared to the fourth quarter of 2023, the majority of which is driven by the launch of liraglutide injection 1.8mg (an authorized generic of Victoza®) and higher revenues from Truxima® (the biosimilar to Rituxan®), partially offset by lower revenues from lenalidomide capsules (the generic version of Revlimid®) and albuterol sulfate inhalation aerosol (our ProAir® authorized generic).

Amonq the most significant qeneric products we sold in the United States in the fourth quarter of 2024 were Truxima® (the biosimilar to Rituxan®), epinephrine injectable solution (the generic equivalent of EpiPen® and EpiPen Jr®), and liraqlutide 1.8 mq injection (an authorized generic of Victoza®).

In the fourth quarter of 2024, according to IQVIA data, our total prescriptions were approximately 68 million, representing 6.9% of total U.S. generic prescriptions.

On February 24, 2024, Alvotech and Teva announced that the FDA approved SIMLANDI (adalimumabryvk) injection, as an interchangeable biosimilar to Humira®, for the treatment of adult rheumatoid arthritis, juvenile idiopathic arthritis, adult psoriatic arthritis, adult ankylosing spondylitis, Crohn's

disease, adult ulcerative colitis, adult plaque psoriasis, adult hidradentis suppurativa and adult uveitis, On May 21, 2024, Alvotech and Teva announced the availability of SIMLANDI in the U.S.

On April 16, 2024, Alvotech and Teva announced that the FDA has approved SELARSDI (ustekinumabaekn) injection for subcutaneous use, as a biosimilar to Stelara®, for the treatment of moderate to severe plaque psoriasis and for active psoriatic arthritis in adults and pediatric patients six years and older. SELARASDI is expected to launch in the U.S. in the first quarter of 2025.

On June 24, 2024, Teva announced the launch of liraglutide injection 1.8mg (an authorized generic of Victoza®) in the United States. Liraglutide injection is indicated to improve glycemic control in adults and pediatric patients aged 10 years and older with type 2 diabetes mellitus and reduce the risk of cardiovascular events in adults with type 2 diabetes mellitus and established cardiovascular disease.

In July 2024, Teva launched paclitaxel protein-bound particles for injectable suspension (albuminbound) (a therapeutically equivalent product to Abraxane®) in the United States for the treatment of breast cancer after failure of combination chemotherapy for metastatic disease, the treatment of locally advanced or metastatic non-small cell lung cancer, and the treatment of patients with metastatic adenocarcinoma of the pancreas.

On October 1, 2024, Teva launched octreotide acetate for injectable suspension, the first generic version of Sandostatin® LAR Depot. Octreotide acetate for injectable suspension is indicated for the treatment of acromeqaly and severe diarrhea associated with carcinoid syndrome, and is available to patients in the U.S.

AJOVY revenues in our United States segment in the fourth quarter of 2024 were \$63 million, an increase of 11% compared to the fourth quarter of 2023, mainly due to growth in volume, partially offset by unfavorable net pricing. In the fourth quarter of 2024, AJOVY's exit market share in the United States in terms of total number of prescriptions was 29.6% compared to 25.7% in the fourth quarter of 2023.

AUSTEDO revenues in our United States segment in the fourth quarter of 2024 increased by 27%, to \$518 million, compared to \$408 million in the fourth quarter of 2023, mainly due to growth in volume, as well as expanded access for patients.

AUSTEDO XR (deutetrabenazine) extended-release tablets were approved by the FDA on February 17, 2023 in three doses of 6, 12 and 24 mg, and became commercially available in the U.S. in May 2023. In May 2024, the FDA approved AUSTEDO XR as a one pill, once-daily treatment option in doses of 30, 36, 42, and 48 mq. In July 2024, the FDA approved the 18 mq dosage for AUSTEDO XR, makinq it a one pill, once-daily option for all available doses. AUSTEDO XR is a once-daily formulation indicated in adults for tardive dyskinesia and chorea associated with Huntington's disease, which is additional to the currently marketed twice-daily AUSTEDO. AUSTEDO XR is protected by 11 Orange Book patents expiring between 2031 and 2041.

UZEDY (risperidone) extended-release injectable suspension revenues in our United States segment in the fourth quarter of 2024 were \$43 million. UZEDY was approved by the FDA on April 28, 2023 for the treatment of schizophrenia in adults, and was launched in the U.S. in May 2023. UZEDY is a subcutaneous, long-acting formulation of risperidone that controls the steady release of risperidone. UZEDY is protected by four Orange Book patents expiring between 2027 and 2040. UZEDY is protected by requlatory exclusivity until April 28, 2026. We are moving forward with plans to launch UZEDY in other countries worldwide. UZEDY faces competition from multiple other products.

BENDEKA and TREANDA (bendamustine) combined revenues in our United States seqment in the fourth quarter of 2024 were \$41 million, a decrease of 21% compared to the fourth quarter of 2023, mainly due to competition from alternative therapies, as well as the entry of qeneric bendamustine

products into the market. The orphan drug exclusivity that had attached to bendamustine products expired in December 2022.

COPAXONE revenues in our United States segment in the fourth quarter of 2024 were \$63 million, a decrease of 13% compared to the fourth quarter of 2023, mainly due to market share erosion and competition, partially offset by a reduction in sales allowance.

Anda revenues from third-party products in our United States segment in the fourth quarter of 2024 increased by 2% to \$402 million, compared to \$394 million in the fourth quarter of 2023, mainly due to higher volume. Anda, our distribution business in the United States, distributes generic, biosimilars and innovative medicines and OTC pharmaceutical products from Teva and various third-party manufacturers to independent retail pharmacy retail chains, hospitals and physician offices in the United States. Anda is able to compete in the distribution market by maintaining a broad portfolio of products, competitive pricing and delivery throughout the United States.

United States Gross Profit

Gross profit from our United States segment in the fourth quarter of 2024 was \$1,097 million, a decrease of 24%, compared to \$1,444 million in the fourth quarter of 2023.

Gross profit marqin for our United States seqment in the fourth quarter of 2024 decreased to 55.6%, compared to 63.7% in the fourth quarter of 2023. This decrease was mainly due to an upfront payment received in the fourth quarter of 2023 related to the collaboration on our duvakitug (anti-TL1A) asset, partially offset by a favorable mix of products, primarily driven by an increase in revenues from AUSTEDO and the sale of certain product rights.

United States Profit

Profit from our United States seqment consists of revenues less cost of sales, R&D expenses, S&M expenses, G&A expenses and any other income related to this segment. Segment profit does not include amortization and certain other items.

Profit from our United States segment in the fourth quarter of 2024 was \$569 million, a decrease of 42% compared to \$974 million in the fourth quarter of 2023. The higher profit in the fourth quarter of 2023 was mainly due to an upfront payment received in relation to the collaboration on our duvakitug (anti-TL1A) asset.

Europe Segment

Our Europe segment includes the European Union, the United Kingdom and certain other European countries.

The following table presents revenues, expenses and profit for our Europe segment for the three months ended December 31, 2024 and 2023:

Three months ended December 31,
2024 2023
(U.S. \$ in millions / % of Segment Revenues)
Revenues S 1.353 100% S 1,344 100%
Cost of sales 561 41.4% 561 41.7%
Gross profit 792 58.6% 783 58.3%
R&D expenses 56 4.2% 52 3.9%
S&M expenses 221 16.3% 203 15.1%
G&A expenses 75 5.6% 67 5.0%
Other loss (income) 2
Segment profit* \$ 438 32.4% \$ 461 34.3%

* Segment profit does not include amortization and certain other items.

§ Represents an amount less than \$0.5 million or 0.5%, as applicable.

Revenues from our Europe segment in the fourth quarter of 2024 were \$1,353 million, an increase of 1%, or \$9 million, compared to the fourth quarter of 2023. In local currency terms, revenues decreased by 2% compared to the fourth quarter of 2023. Our lower revenues in local currency terms in the fourth quarter of 2024 were mainly due to higher sales of certain product rights in the fourth quarter of 2023, partially offset by higher revenues from generic and OTC products as well as AJOVY.

In the fourth quarter of 2024, revenues were positively impacted by exchange rate fluctuations of \$33 million, net of hedging effects, compared to the fourth quarter of 2023. Revenues in the fourth quarter of 2024, included \$20 million from a positive hedging impact, which is included in "Other" in the table below. Revenues in the fourth quarter of 2023 included \$20 million from a negative hedging impact, which is included in "Other" in the table below.

Revenues by Major Products and Activities

The following table presents revenues for our Europe segment by major products and activities for the three months ended December 31, 2024 and 2023:

Three months ended
December 31,
Percentage
Change
2024 2023 2024-2023
(U.S. \$ in millions)
Generic products (including OTC and
biosimilars) . \$ 2 938 4%
AJOVY 58 45 28%
COPAXONE 50 ટેર (11%)
Respiratory products 61 70 (13%)
Other* 205 234 (12%)
Total 1,353 \$ 1,344 1%

*Other revenues in the fourth quarter of 2024 and 2023 include the sale of certain product rights.

Generic products revenues (including OTC and biosimilar products) in our Europe segment in the fourth quarter of 2024, were \$979 million, an increase of 4% compared to the fourth quarter of 2023. In local currency terms, revenues increased by 5%, mainly due to price increases as a result of market conditions such as inflationary pressures in certain markets, as well as higher revenues from recently launched products.

AJOVY revenues in our Europe segment in the fourth quarter of 2024 were \$58 million, an increase of 28% in both U.S. dollars and local currency terms, compared to the fourth quarter of 2023. This increase was due to growth in volume.

COPAXONE revenues in our Europe segment in the fourth quarter of 2024 were \$50 million, a decrease of 11% in both U.S. dollars and local currency terms, compared to the fourth quarter of 2023. This decrease was mainly due to price reductions and a decline in volume resulting from availability of alternative therapies and competing glatiramer acetate products.

Respiratory products revenues in our Europe segment in the fourth quarter of 2024 were \$61 million, a decrease of 13% in both U.S. dollars and local currency terms, compared to the fourth quarter of 2023. This decrease was mainly due to net price reductions and lower volumes.

Europe Gross Profit

Gross profit from our Europe segment in the fourth quarter of 2024 was \$792 million, an increase of 1% compared to \$783 million in the fourth quarter of 2023.

Gross profit margin for our Europe segment in the fourth quarter of 2024 increased to 58.6%, compared to 58.3% in the fourth quarter of 2023. This increase was mainly due to positive impact from hedging activities.

Europe Profit

Profit from our Europe seqment consists of revenues less cost of sales, R&D expenses, G&A expenses and any other income related to this segment profit does not include amortization and certain other items.

Profit from our Europe segment in the fourth quarter of 2024 was \$438 million, a decrease of 5%, compared to \$461 million in the fourth quarter of 2023. This decrease was mainly due to higher S&M expenses to support revenue growth.

International Markets Segment

Our International Markets segment includes all countries in which we operate other than the United States and the countries included in our Europe seqment. The International Markets segment covers a substantial portion of the global pharmaceutical industry, including more than 35 countries.

As part of a recent shift in executive management responsibilities, commencing January 1, 2024, Canada is reported under our International Markets segment and is no longer included as part of our United States segment. Prior period amounts were recast to reflect this change.

On December 5, 2024, we announced that we entered into an agreement with JKI Co. Ltd., established by the fund managed and operated by private equity firm J-Will Partners Co. Ltd., to sell our business venture in Japan (the "BV"), which includes generic products and legacy products, with an expected closing date of April 1, 2025, subject to standard closing conditions.

Since the establishment of the BV and as of December 31, 2024, Teva holds 51% of the outstanding common stock of the BV, therefore consolidating the BV in our financial statements.

The following table presents revenues, expenses and profit for our International Markets segment for the three months ended December 31, 2024 and 2023:

Three months ended December 31,
2024 2023
(U.S. \$ in millions / % of Segment Revenues)
Revenues S 661 100% \$ 601 100%
Cost of sales 315 47.7% 302 50.2%
Gross profit 346 52.3% 299 49.8%
R&D expenses 27 4.1% 24 3.9%
S&M expenses 137 20.7% 134 22.2%
G&A expenses 42 6.3% 37 6.2%
Other loss (income) (1) (4) (0.7%)
Seqment profit* \$ 141 21.4% 109 18.1%

* Segment profit does not include amortization and certain other items.

§ Represents an amount less than \$0.5 million or 0.5%, as applicable.

Revenues from our International Markets segment in the fourth quarter of 2024 were \$661 million, an increase of 10% compared to the fourth quarter of 2023. In local currency terms, revenues increased by 17% compared to the fourth quarter of 2023, mainly due to revenues from the sale of certain product rights, higher revenues from generic products in most markets, partially offset by regulatory price reductions and generic competition to off-patented products in Japan.

In the fourth quarter of 2024, revenues were negatively impacted by exchange rate fluctuations of \$40 million, net of hedging effects, compared to the fourth quarter of 2023. Revenues in the fourth quarter of 2024 included \$13 million from a positive hedging impact, compared to a negative hedging impact of \$3 million in the fourth quarter of 2023, which are included in "Other" in the table below.

Revenues by Major Products and Activities

The following table presents revenues for our International Markets segment by major products and activities for the three months ended December 31, 2024 and 2023:

Three months ended
December 31.
Percentage
Change
2024 2023 2024-2023
(U.S. \$ in millions)
Generic products (including OTC and
biosimilars) \$ 506 (2%)
AJOVY 22 19 16%
COPAXONE 12 (25%)
AUSTEDO 7 5 50%
Other* 126 60 112%
Total 5 661 601 10%

*Other revenues in the fourth quarter of 2024 include the sale of certain product rights.

Generic products revenues (including OTC and biosimilar products) in our International Markets segment were \$497 million in the fourth quarter of 2024, a decrease of 2% compared to the fourth quarter of 2023. In local currency terms, revenues increased by 8% compared to the fourth quarter of 2023, mainly due to higher revenues in most markets, largely driven by price increases as a result of higher costs due to inflationary pressure in certain markets and higher volumes, partially offset by regulatory price reductions and generic competition to off-patented products in Japan.

AJOVY was launched in certain markets in our International Markets seqment, including in Canada, Japan, Australia, Israel, South Korea, Brazil and others. AJOVY revenues in our International Markets seqment in the fourth quarter of 2024 were \$22 million, compared to \$19 million in the fourth quarter of 2023. In local currency terms, revenues increased by 22%, due to growth in existing markets in which AJOVY was launched.

COPAXONE revenues in our International Markets segment in the fourth quarter of 2024 were \$9 million compared to \$12 million in the fourth quarter of 2023. In local currency terms, revenues decreased by 16% mainly due to market share erosion and competition.

AUSTEDO was launched in China and Israel in 2021 and in Brazil in 2022, for the treatment of chorea associated with Huntington's disease and for the treatment of tardive dyskinesia. In February 2024, we announced a strategic partnership for the marketing and distribution of AUSTEDO in China. We continue with additional submissions in various other markets.

AUSTEDO revenues in our International Markets seqment in the fourth quarter of 2024 were \$7 million, In local currency terms, revenues increased by 54%, substantially due to the launch of a strategic partnership in China.

International Markets Gross Profit

Gross profit from our International Markets segment in the fourth quarter of 2024 was \$346 million, an increase of 16% compared to \$299 million in the fourth quarter of 2023.

Gross profit margin for our International Markets segment in the fourth quarter of 2024 increased to 52.3%, compared to 49.8% in the fourth quarter of 2023. This increase was mainly due to revenues from the sale of certain product rights, price increases largely as a result of inflationary pressures in certain markets, a positive hedging impact and a favorable mix of products, partially offset by regulatory price reductions and generic competition to off-patented products in Japan, as well as higher costs due to inflationary and other macroeconomic pressures.

International Markets Profit

Profit from our International Markets segment consists of revenues less cost of sales, R&D expenses, S&M expenses, G&A expenses and any other income related to this segment. Segment profit does not include amortization and certain other items.

Profit from our International Markets segment in the fourth quarter of 2024 was \$141 million, an increase of 30%, compared to \$109 million in the fourth quarter of 2023. This increase was mainly due to higher gross profit, as mentioned above.

Other Activities

We have other sources of revenues, primarily the sale of APIs to third parties, certain contract manufacturing services and an out-licensing platform offering a portfolio of products to other pharmaceutical companies through our affiliate Medis. Our other activities are not included in our United States, Europe or International Markets segments described above.

On January 31, 2024, we announced that we intend to divest our API business (including its R&D, manufacturing and commercial activities) through a sale. The intention to divest is in alignment with our Pivot to Growth strategy. However, there can be no assurance regarding the ultimate timing or structure of the potential divestiture or that a divestiture will be agreed or completed at all.

Revenues from other activities in the fourth quarter of 2024 were \$241 million, a decrease of 2% in both U.S. dollars and local currency terms, compared to the fourth quarter of 2023.

API sales to third parties in the fourth quarter of 2024 were \$145 million, flat compared to the fourth quarter of 2023, following a reallocation of an immaterial business within our other activities, in line with our intention to divest our API business.

2025 Non-GAAP Outlook
\$ billions, except diluted EPS or
as noted
2025 Outlook
Revenues* 16.8 -17.4
AUSTEDO (\$m)* 1,900-2,050
AJOVY (Şm)* ~600
UZEDY (\$m)* ~160
COPAXONE (\$m)* ~370
Operating Income 4.1 - 4.6
Adjusted EBITDA 4.5 - 5.0
Finance Expenses (\$m) ~900
Tax Rate 15% - 18%
Diluted EPS (S) 2.35-2.65
Free Cash Flow** 1.6 - 1.9
CAPEX* ~0.5
Foreian Exchange Volatile swings in FX can negatively

impact revenue and income

* Revenues and CAPEX presented on a GAAP basis.

** Free Cash Flow includes cash flow generated from operating activities net of capital expenditures and deferred purchase price cash component collected for securitized trade receivables

Annual Report on Form 10-K

Teva's Annual Report on Form 10-K for the year ended December 31, 2024, which will be filed with the SEC, will include a complete analysis of the financial results for 2023 and will be available on Teva's website: http://ir.tevapharm.com, as well as on the SEC's website: http://www.sec.qov.

Conference Call

Teva will host a conference call and live webcast along with a slide presentation on Wednesday, January 29, 2025 at 8:00 a.m. ET to discuss its fourth quarter and annual 2024 results and overall business environment. A question & answer session will follow.

In order to participate, please register in advance here to obtain a local or toll-free phone number and your personal pin.

A live webcast of the call will be available on Teva's website at: http://ir.tevapharm.com/.

Following the conclusion of the call, a replay of the webcast will be available within 24 hours on Teva's website.

About Teva

  • ;

Consolidated Statements of Income (U.S. dollars in millions, except share and per share data)

Three months ended
December 31,
Year ended
December 31,
(Unaudited)
2024 2023 2024 2023
Net revenues 4,229 4,457 16,544 15,846
Cost of sales 2,109 2,041 8,481 8,200
Gross profit 2,120 2,416 8,064 7,645
Research and development expenses 248 227 998 953
Selling and marketing expenses 650 610 2,541 2,336
General and administrative expenses 302 291 1,161 1162
Intangible assets impairments 81 61 251 350
Goodwill impairment 280 - 1,280 700
Other asset impairments, restructuring and other items 457 443 1,388 718
Legal settlements and loss contingencies 123 34 761 1,043
Other (income) loss 8 (6) (14) (49)
Operating income (loss) (29) 755 (303) 433
Financial expenses, net 218 249 981 1,057
Income (loss) before income taxes (247) 507 (1,284) (624)
Income taxes (benefit) 29 43 676 (7)
Share in (profits) losses of associated companies, net (1) (1) (1) (2)
Net income (loss) (275) 465 (1,959) (615)
Net income (loss) attributable to non-controlling interests (58) 4 (320) (56)
Net income (loss) attributable to Teva (217) 461 (1,639) (559)
Earnings (loss) per share attributable to Teva: Basic (\$) (0.19) 0.41 (1.45) (0.50)
Diluted (\$) (0.19) 0.41 (1.45) (0.50)
Weighted average number of shares (in millions): Basic 1,133 1,121 1,131 1,119
Diluted 1,133 1,137 1,131 1,119
Non-GAAP net income attributable to Teva for diluted earnings per share:* 816 1,135 2,860 2,898
Non-GAAP earnings per share attributable to Teva:* Diluted (\$) 0.71 1.00 2.49 2.56
Non-GAAP average number of shares (in millions): Diluted 1,157 1,137 1,150 1,131

Amounts may not add up due to rounding.

§ Represents an amount less than \$0.5 million.

* See reconciliation attached.

Condensed Consolidated Balance Sheets

(U.S. dollars in millions)

(Audited)

December 31, December 31,
ASSETS 2024 2023
Current assets:
Cash and cash equivalents 3,300 3,226
Accounts receivables, net of allowance for credit losses of \$78
million and \$95 million as of December 31, 2024 and December
31, 2023 3,059 3,408
Inventories 3,007 4,021
Prepaid expenses 1,006 1,255
Other current assets 409 504
Assets held for sale 1,771 70
Total current assets 12,552 12,485
Deferred income taxes 1,799 1,812
Other non-current assets 462 470
Property, plant and equipment, net 4,581 5,750
Operating lease right-of-use assets 367 397
Identifiable intangible assets, net 4,418 5,387
Goodwill 15,147 17,177
Total assets 39,326 43,479
LIABILITIES & EQUITY
Current liabilities:
Short-term debt 1,781 1,672
Sales reserves and allowances 3,678 3,535
Trade payables 2,203 2,602
Employee-related obligations 624 611
Accrued expenses 2,792 2,771
Other current liabilities 1,020 1,044
Liabilities held for sale 698 13
Total current liabilities 12,796 12,247
Long-term liabilities:
Deferred income taxes 483 606
Other taxes and long-term liabilities 4,028 4,019
Senior notes and loans 16,002 18,161
Operating lease liabilities 296 320
Total long-term liabilities 20,809 23,106
Redeemable non-controlling interests 340 -
Equity:
Teva shareholders' equity: 5,373 7,506
Non-controlling interests 7 620
Total equity 5,380 8,126
Total liabilities and equity 39,326 43,479

TEVA PHARMACEUTICAL INDUSTRIES LIMITED CONSOLIDATED STATEMENTS OF CASH FLOWS (U.S. dollars in millions)

Year ended
December 31,
Three months ended
December 31,
(Unaudited)
2024 2023 2024 2023
(Audited) (Audited) (Unaudited) (Unaudited)
Operating activities:
Net income (loss) (1,959) (615) \$
(275)
\$
465
Adjustments to reconcile net income (loss) to net cash provided by operations:
Impairment of goodwil 1,280 700 280 -
Impairment of long-lived assets and assets held for sale 1,275 378 517 68
Depreciation and amortization 1,059 1,153 269 266
Net change in operating assets and liabilities (435) (72) (246) 292
Deferred income taxes — net and uncertain tax positions (634) (317) 32 34
Stock-based compensation 123 121 34 28
Net loss (gain) from sale of business and long-lived assets (22) (41) - (10)
Other items * 560 61 (37) 41
Net cash provided by (used in) operating activities 1,247 1,368 575 1,184
Investing activities:
Beneficial interest collected in exchange for securitized trade receivables 1,291 1,477 340 421
Purchases of property, plant and equipment and intangible assets (498) (526) (129) (120)
Proceeds from sale of business and long lived assets 43 68 4 -
Purchases of investments and other assets (71) (46) (15) (2)
Proceeds from sale of investments 40 - - -
Acquisitions of businesses, net of cash acquired (15) - - -
Other investing activities 2 (5) 2 2
Net cash provided by (used in) investing activities 792 968 202 301
Financing activities:
Repayment of senior notes and loans and other long term liabilities (1,641) (4,152) (685) -
Proceeds from senior notes, net of issuance costs - 2,451 - -
Proceeds from short term debt - 700 - -
Repayment of short term debt - (700) - (500)
Purchase of shares from non-controlling interests (64) - - -
Dividends paid to non-controlling interests (78) - - -
Other financing activities (8) (212) 10 (76)
Net cash provided by (used in) financing activities (1,791) (1,913) (675) (576)
Translation adjustment on cash and cash equivalents (174) (30) (121) 68
Net change in cash, cash equivalents and restricted cash \$ 74 \$
393
\$
(19)
\$
977
Balance of cash, cash equivalents and restricted cash at beginning of year 3,227 2,834 3,319 2,250
Balance of cash, cash equivalents and restricted cash at end of year 3,300 3,227 3,300 3,227
Reconciliation of cash, cash equivalents and restricted cash reported in the consolidated balance sheets:
Cash and cash equivalents 3,300 3,226 3,300 3,226
Restricted cash included in other current assets - 1 - 1
Total cash, cash equivalents and restricted cash shown in the statements of cash flows 3,300 3,227 3,300 3,227

Reconciliation of net income (loss) attributable to Teva to Non-GAAP net income (loss) attributable to Teva

(\$ in millions except per share amounts) Three months ended
December 31,
2024
2023 2024 Year ended
December 31,
2023
Net income (Loss) attributable to Teva (\$) (217) 461 (\$) (1,639) (559)
Increase (decrease) for excluded items:
Amortization of purchased intangible assets 144 144 588 616
Legal settlements and loss contingencies(1) 123 34 761 1,043
Goodwill impairment(2) 280 - 1,280 700
Impairment of long-lived assets(3) 517 68 1,275 378
Restructuring costs 22 18 74 111
Equity compensation 34 28 123 121
Contingent consideration(4) (2) 408 303 548
Loss (Gain) on sale of business 6 - (15) (3)
Accelerated depreciation 5 6 13 80
Financial expenses 13 13 49 66
Items attributable to non-controlling interests(3) (63) (1) (339) (92)
Other non-GAAP items(5) 67 83 229 335
Corresponding tax effects and unusual tax items(6) (114) (128) 157 (446)
Non-GAAP net income attributable to Teva (\$) 816 1,135 (\$) 2,860 2,898
Non-GAAP tax rate(7) 14.8% 13.1% 15.3% 13.0%
GAAP diluted earnings (loss) per share attributable to Teva (\$) (0.19) 0.41 (\$) (1.45) (0.50)
EPS difference(8) 0.90 0.59 3.94 3.06
Non-GAAP diluted EPS attributable to Teva(8) (\$) 0.71 1.00 (\$) 2.49 2.56
Non-GAAP average number of shares (in millions)(8) 1,157 1,137 1,150 1,131

(1) Adjustments for legal settlements and loss contingencies in 2024 were mainly related to a legal expenses of \$357 million recorded in connection with a decision by the European Commission in its antitrust investigation into COPAXONE, and to an update to the estimated settlement provision of \$278 million for the opioid cases (mainly the effect of the passage of time on the net present value of the discounted payments and the settlement agreement with the city of Baltimore). Adjustments for legal settlements and loss contingencies in 2023 were mainly related to an update to the estimated provision of \$370 million related to the DOJ patient assistance program litigation, an update to the estimated settlement provision of \$269 million related to the remaining opioid cases, the provision of \$207 million relating to the U.S. DOJ criminal antitrust charges on the marketing and pricing of certain Teva USA generic products and the provision of \$100 million related to the settlement of the reverse-payment antitrust litigation over certain HIV medicines.

  • (2) During the fourth quarter of 2024 a goodwill impairment charge of \$280 million was recorded related to our API reporting unit. During the year ended December 31, 2024 goodwill impairment charges of \$1,280 million were recorded related to our API reporting unit. During the year ended December 31, 2023 goodwill impairment charges of \$700 million were recorded related to our International Markets reporting unit.
  • (3) Adjustments for impairment of long-lived assets and items attributable to non-controlling interests, in the fourth quarter of 2024 primarily consisted of \$129 million and \$63 million, respectively, related to the classification of the business venture in Japan as held for sale. In addition, in the fourth quarter of 2024 we recognized an impairment of \$275 million related to the classification of our API business (including its R&D, manufacturing and commercial activities) as held for sale. Adjustments for impairment of long-lived assets and items attributable to non-controlling interests, for the year ended December 31, 2024 primarily consisted of \$689 million and \$339 million, respectively, related to the classification of the business venture in Japan as held for sale. In addition, in 2024 we recognized an impairment of \$275 million related to the classification of our API business (including its R&D, manufacturing and commercial activities) as held for sale.
  • (4) During the fourth quarter of 2024 and 2023 adjustments for contingent consideration primarily related to a change in the estimated future royalty payments to Allergan in connection with lenalidomide capsules (the generic version of Revlimid®), of \$3 million and \$311 million, respectively. During the year ended December 31, 2024 and 2023 adjustments for contingent consideration primarily related to a change in the estimated future royalty payments to Allergan in connection with lenalidomide capsules (the generic version of Revlimid®), of \$270 million and \$422 million, respectively.
  • (5) Other non-GAAP items include other exceptional items that we believe are sufficiently large that their exclusion is important to facilitate an understanding of trends in our financial results, primarily related to the rationalization of our plants, certain inventory write-offs, material litigation fees and other unusual events.
  • (6) Adjustments for corresponding tax effects and unusual tax items for the year ended December 31, 2024, include a tax item in an amount of \$495 million related to the settlement agreement with the ITA to settle certain litigation with respect to taxes payable for the Company's taxable years 2008 through 2020.
  • (7) Non-GAAP tax rate is tax expenses (benefit) excluding the impact of non-GAAP tax adjustments presented above as a percentage of income (loss) before income taxes excluding the impact of non-GAAP adjustments presented above.
  • (8) EPS difference and diluted non-GAAP EPS are calculated by dividing our non-GAAP net income attributable to Teva by our non-GAAP diluted weighted average number of shares.

Reconciliation of gross profit to Non-GAAP gross profit

Three months ended Year ended
December 31, December 31,
(\$ in millions) 2024 2023 2024 2023
GAAP gross profit (\$) 2,120 2,416 (\$) 8,064 7,645
GAAP gross profit margin 50.1% 54.2% 48.7% 48.2%
Increase (decrease) for excluded items:(1)
Amortization of purchased intangible assets 135 129 543 549
Costs related to regulatory actions taken in facilities 3 2 8 4
Equity compensation 5 4 23 19
Accelerated Depreciation 5 6 13 80
Other non-GAAP items 51 35 164 173
Non-GAAP gross profit (\$) 2,319 2,592 (\$) 8,814 8,470
Non-GAAP gross profit margin(2) 54.8% 58.2% 53.3% 53.5%

(1) For further explanations, refer to the footnotes under the "Reconciliation of net income (loss) attributable to Teva to Non-GAAP net income (loss) attributable to Teva" table.

(2) Non-GAAP gross profit margin is non-GAAP gross profit as a percentage of revenue.

Reconciliation of operating income (loss) to Non-GAAP operating income (loss)

Three months ended Year ended,
December 31, December 31,
(\$ in millions) 2024 2023 2024 2023
Operating income (loss) (\$) (29) 755 (\$) (303) 433
Operating margin (0.7%) 17.0% (1.8%) 2.7%
Increase (decrease) for excluded items: (1)
Amortization of purchased intangible assets 144 144 588 616
Legal settlements and loss contingencies 123 34 761 1,043
Goodwill impairment 280 - 1,280 700
Impairment of long-lived assets 517 68 1,275 378
Restructuring costs 22 18 74 111
Equity compensation 34 28 123 121
Contingent consideration (2) 408 303 548
Loss (gain) on sale of business 6 - (15) (3)
Accelerated depreciation 5 6 13 80
Other non-GAAP items 67 84 229 336
Non-GAAP operating income (loss) (\$) 1,168 1,546 (\$) 4,329 4,361
Non-GAAP operating margin(2) (\$) 27.6% 34.7% (\$) 26.2% 27.5%

(1) For further explanations, refer to the footnotes under the "Reconciliation of net income (loss) attributable to Teva to Non-GAAP net income (loss) attributable to Teva" table.

(2) Non-GAAP operating margin is Non-GAAP operating income as a percentage of revenues.

Reconciliation of net income (loss) to adjusted EBITDA

Three months ended Year ended
December 31, December 31,
(\$ in millions) 2024 2023 2024 2023
Net income (loss) \$ (275) 465 \$ (1,959) (615)
Increase (decrease) for excluded items:(1)
Financial expenses 218 249 981 1,057
Income taxes 29 43 676 (7)
Share in profits (losses) of associated companies –net (1) (1) (1) (2)
Depreciation 119 120 465 537
Amortization 144 144 588 616
EBITDA 235 1,020 750 1,585
Legal settlements and loss contingencies 123 34 761 1,043
Goodwill impairment 280 - 1,280 700
Impairment of long lived assets 517 68 1,275 378
Restructuring costs 22 18 74 111
Equity compensation 34 28 123 121
Contingent consideration (2) 408 303 548
Loss (Gain) on sale of Business 6 - (15) (3)
Other non-GAAP items 67 84 229 335
Adjusted EBITDA \$ 1,282 1,660 \$ 4,781 4,818

(1) For further explanations, refer to the footnotes under the "Reconciliation of net income (loss) attributable

to Teva to Non-GAAP net income (loss) attributable to Teva" table.

Segment Information

United States Europe International Markets
Three months ended
December 31,
Three months ended
December 31,
Three months ended
December 31,
2024 2023 2024 2023 2024 2023
(U.S. \$ in millions) (U.S. \$ in millions) (U.S. \$ in millions)
Revenues \$ 1,975 \$ 2,266 \$ 1,353 \$ 1,344 \$ 661 \$ 601
Cost of sales 877 822 561 561 315 302
Gross profit 1,097 1,444 792 783 346 299
R&D expenses 158 144 56 52 27 24
S&M expenses 260 238 221 203 137 134
G&A expenses 109 90 75 67 42 37
Other income 1 (1) 2 § (1) (4)
Segment profit \$ 569 \$ 974 \$ 438 \$ 461 \$ 141 \$ 109

§ Represents an amount less than \$0.5 million.

Segment Information

United States Europe
Year ended December 31,
International Markets
Year ended December 31,
Year ended December 31,
2024 2023 2024 2023 2024 2023
(U.S. \$ in millions) (U.S. \$ in millions) (U.S. \$ in millions)
Revenues \$ 8,034 \$ 7,731 \$ 5,103 \$ 4,837 \$ 2,463 \$ 2,351
Cost of sales 3,646 3,421 2,197 2,111 1,229 1,191
Gross profit 4,388 4,310 2,905 2,726 1,235 1,160
R&D expenses 633 604 229 220 112 104
S&M expenses 1,049 938 826 767 534 487
G&A expenses 410 378 272 263 150 142
Other income § (5) 3 (2) (2) (39)
Segment profit \$ 2,296 \$ 2,394 \$ 1,575 \$ 1,478 \$ 440 \$ 465

Reconciliation of our segment profit to consolidated income (loss) before income taxes

Three months ended
December 31,
2024 2023
(U.S.\$ in millions)
United States profit \$ 569 \$ 974
Europe profit 438 461
International Markets profit 141 109
Total reportable segment profit 1,148 1,544
Profit (loss) of other activities 19 2
1,168 1,546
Amounts not allocated to segments:
Amortization 144 144
Other asset impairments, restructuring and other items 458 443
Goodwill impairment 280 -
Intangible asset impairments 81 61
Legal settlements and loss contingencies 123 34
Other unallocated amounts 110 108
Consolidated operating income (loss) (29) 755
Financial expenses - net 218 249
Consolidated income (loss) before income taxes \$ (247) \$ 507

Reconciliation of our segment profit to consolidated income (loss) before income taxes

Year ended
December 31,
2024 2023
(U.S.\$ in millions)
United States profit \$ 2,296 \$ 2,394
Europe profit 1,575 1,478
International Markets profit 440 465
Total reportable segment profit 4,311 4,338
Profit (loss) of other activities 18 24
Total segment profit 4,329 4,361
Amounts not allocated to segments:
Amortization 588 616
Other asset impairments, restructuring and other items 1,388 718
Goodwill impairment 1,280 700
Intangible asset impairments 251 350
Legal settlements and loss contingencies 761 1,043
Other unallocated amounts 364 502
Consolidated operating income (loss) (303) 433
Financial expenses - net 981 1,057
Consolidated income (loss) before income taxes \$ (1,284) \$ (624)

Segment revenues by major products and activities

December 31, Percentage
Change
2024 2023 2023-2024
(U.S.\$ in millions)
United States segment
Generic products \$ 674 \$ 667 1%
AJOVY 63 57 11%
AUSTEDO 518 408 27%
BENDEKA/TREANDA 41 52 (21%)
COPAXONE 63 72 (13%)
UZEDY 43 9 N/A
Anda 402 394 2%
Other* 171 607 (72%)
Total 1,975 2,266 (13%)

*Other revenues in the fourth quarter of 2024 include the sale of certain product rights. Other revenues in 2023 were mainly comprised of a \$500 million upfront payment received in the fourth quarter of 2023, in connection with the collaboration on our duvakitug (anti-TL1A) asset.

Three months ended
Percentage
Change
2024 December 31, 2023 2023-2024
(U.S.\$ in millions)
Europe segment
Generic products \$
979
\$ 938 4%
AJOVY 58 45 28%
COPAXONE 50 56 (11%)
Respiratory products 61 70 (13%)
Other* 205 234 (12%)
Total 1,353 1,344 1%

*Other revenues in the fourth quarter of 2024 and 2023 include the sale of certain product rights.

Three months ended
December 31, Percentage
Change
2024 2023 2023-2024
(U.S.\$ in millions)
International Markets segment
Generic products \$
497
\$ 506 (2%)
AJOVY 22 19 16%
COPAXONE 9 12 (25%)
AUSTEDO 7 5 50%
Other* 126 60 112%
Total 661 601 10%

*Other revenues in the fourth quarter of 2024 include the sale of certain product rights.

Segment revenues by major products and activities

Year ended Percentage
Change
December 31,
2024 2023 2024-2023
(U.S.\$ in millions)
United States segment
Generic products \$ 3,599 \$ 3,138 15%
AJOVY 207 211 (2%)
AUSTEDO 1,642 1,225 34%
BENDEKA / TREANDA 168 237 (29%)
COPAXONE 242 297 (18%)
UZEDY 117 23 N/A
Anda 1,536 1,577 (3%)
Other* 523 1,025 (49%)
Total 8,034 7,731 4%

*Other revenues in 2024 include the sale of certain product rights. Other revenues in 2023 were mainly comprised of a \$500 million upfront payment received in the fourth quarter of 2023, in connection with the collaboration on our duvakitug (anti-TL1A) asset.

Year ended Percentage
Change
December 31,
2024 2023 2024-2023
(U.S.\$ in millions)
Europe segment
Generic products \$ 3,926 \$ 3,664 7%
AJOVY 216 160 34%
COPAXONE 213 231 (8%)
Respiratory products 244 265 (8%)
Other* 504 516 (2%)
Total 5,103 4,837 5%

*Other revenues in 2024 and 2023 include the sale of certain product rights.

Year ended
December 31,
Percentage
Change
2024 2023 2024-2023
(U.S.\$ in millions)
International Markets segment
Generic products \$ 1,937 \$ 1,932 0%
AJOVY 84 63 33%
COPAXONE 48 63 (24%)
Austedo 46 15 199%
Other* 349 278 25%
Total 2,463 2,351 5%

*Other revenues in 2024 include the sale of certain product rights.

Free cash flow reconciliation

Three months ended December 31,
2024 2023
(U.S. \$ in millions)
Net cash provided by (used in) operating activities 575 1,184
Beneficial interest collected in exchange for securitized account receivables 340 421
Purchases of property, plant and equipment and intangible assets (129) (120)
Proceeds from divestitures of businesses and other assets 4 -
Free cash flow \$ 790 \$
1,486

Free cash flow reconciliation

Year ended December 31
2024 2023
(U.S. \$ in millions)
Net cash provided by (used in) operating activities 1,247 1,368
Beneficial interest collected in exchange for securitized account receivables 1,291 1,477
Purchases of property, plant and equipment and intangible assets (498) (526)
Acquisition of businesses, net of cash acquired (15) -
Proceeds from divestitures of businesses and other assets 43 68
Free cash flow \$ 2,068 \$
2,387

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