01/22/2025 | Press release | Distributed by Public on 01/22/2025 15:55
Media contact:
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Investor contact:
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Q4
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Full Year
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|||||||
($ in Millions, expect EPS)
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2024
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2023
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% Change
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2024
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2023
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% Change
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Reported Sales
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$22,520
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$ 21,395
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5.3%
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$88,821
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$ 85,159
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4.3%
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Net Earnings
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$3,431
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$4,132
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(17.0)%
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$14,066
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$13,326
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5.6%
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EPS (diluted)
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$1.41
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$1.70
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(17.1)%
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$5.79
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$5.20
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11.3%
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Q4
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Full Year
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||||||
Non-GAAP* ($ in Millions, except EPS)
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2024
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2023
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% Change
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2024
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2023
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% Change
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Operational Sales1,2
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6.7%
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5.9%
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Adjusted Operational Sales1,3
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5.7%
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5.4%
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Adjusted Operational Sales1,3 ex. COVID-19 Vaccine
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5.9%
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6.5%
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Adjusted Net Earnings1,4
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$4,946
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$5,562
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(11.1)%
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$ 24,242
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$ 25,409
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(4.6)%
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Adjusted EPS (diluted)1,4
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$2.04
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$2.29
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(10.9)%
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$9.98
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$9.92
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0.6%
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Free Cash Flow6,7
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~$19,800
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$18,248
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Q4
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% Change
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($ in Millions)
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2024
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2023
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Reported
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Operational1,2
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Currency
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Adjusted
Operational1,3
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U.S.
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$13,204
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$12,009
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10.0%
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10.0
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-
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8.6
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International
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9,316
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9,386
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(0.7)
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2.5
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(3.2)
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2.0
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Worldwide
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$22,520
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$21,395
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5.3%
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6.7
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(1.4)
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5.7
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Full Year
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% Change
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($ in Millions)
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2024
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2023
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Reported
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Operational1,2
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Currency
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Adjusted
Operational1,3
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U.S.
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$50,302
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$46,444
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8.3%
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8.3
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-
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7.6
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International
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38,519
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38,715
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(0.5)
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2.9
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(3.4)
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2.7
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Worldwide
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$88,821
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$85,159
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4.3%
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5.9
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(1.6)
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5.4
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Q4
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% Change
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($ in Millions)
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2024
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2023
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Reported
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Operational1,2
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Currency
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Adjusted
Operational1,3
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Innovative Medicine
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$14,332
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$13,722
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4.4%
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6.1
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(1.7)
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6.3
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MedTech
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8,188
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7,673
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6.7
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7.6
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(0.9)
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4.6
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Worldwide
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$22,520
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$21,395
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5.3%
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6.7
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(1.4)
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5.7
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Full Year
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|
|
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% Change
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|
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($ in Millions)
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2024
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2023
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Reported
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Operational1,2
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Currency
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Adjusted
Operational1,3
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Innovative Medicine
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$56,964
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$54,759
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4.0%
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5.7
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(1.7)
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5.8
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MedTech
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31,857
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30,400
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4.8
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6.2
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(1.4)
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4.7
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Worldwide
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$88,821
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$85,159
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4.3%
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5.9
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(1.6)
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5.4
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($ in Billions, except EPS)
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January 2025
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Adjusted Operational Sales1,2,5
Change vs. Prior Year / Mid-point
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2.0% - 3.0% / 2.5%
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Operational Sales2,5 / Mid-point
Change vs. Prior Year / Mid-point
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$90.9B - $91.7B / $91.3B
2.5% - 3.5% / 3.0%
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Estimated Reported Sales3,5/ Mid-point
Change vs. Prior Year / Mid-point
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$89.2B - $90.0B / $89.6B
0.5% - 1.5% / 1.0%
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Adjusted Operational EPS (Diluted)2,4 / Mid-point
Change vs. Prior Year / Mid-point
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$10.75 - $10.95 / $10.85
7.7% - 9.7% / 8.7%
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Adjusted EPS (Diluted)3,4 / Mid-point
Change vs. Prior Year / Mid-point
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$10.50 - $10.70 / $10.60
5.2% - 7.2% / 6.2%
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Regulatory |
SPRAVATO (esketamine) approved in the U.S. as the first and only monotherapy for adults with treatment-resistant depression1
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European Commission approves LAZCLUZE (lazertinib) in combination with RYBREVANT (amivantamab) for the first-line treatment of patients with EGFR-mutated advanced non-small cell lung cancer1
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New Drug Application initiated with U.S. FDA for TAR-200, the first and only intravesical drug releasing system for patients with BCG-unresponsive high-risk non-muscle-invasive bladder cancer1
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Johnson & Johnson MedTech Announces CE Mark Approval for Dual Energy THERMOCOOL SMARTTOUCH SF Catheter1
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Nipocalimab granted U.S. FDA Priority Review for the treatment of generalized myasthenia gravis1
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Johnson & Johnson's Posdinemab and Tau Active Immunotherapy Receive U.S. FDA Fast Track Designations for the Treatment of Alzheimer's Disease1
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European Commission approves RYBREVANT (amivantamab) in combination with LAZCLUZE (lazertinib) for the first-line treatment of patients with EGFR-mutated advanced non-small cell lung cancer | ||
Johnson & Johnson submits application to the European Medicines Agency seeking approval of a new indication for IMBRUVICA (ibrutinib) in adult patients with previously untreated mantle cell lymphoma (MCL) who are eligible for autologous stem cell transplant | ||
U.S. FDA Expands Indication for Impella Heart Pumps to Treat Pediatric Patients | ||
Johnson & Johnson seeks U.S. FDA approval for first pediatric indications for TREMFYA (guselkumab) | ||
Johnson & Johnson seeks U.S. FDA approval for subcutaneous induction regimen of TREMFYA (guselkumab) in ulcerative colitis, a first for an IL-23 inhibitor | ||
Johnson & Johnson MedTech Receives IDE Approval for OTTAVA Robotic Surgical System | ||
Nipocalimab is the first and only investigational therapy granted U.S. FDA Breakthrough Therapy Designation for the treatment of adults living with moderate-to-severe Sjögren's disease | ||
Johnson & Johnson submits applications in the U.S. and EU seeking approval of DARZALEX FASPRO / DARZALEX as subcutaneous monotherapy for high-risk smoldering multiple myeloma | ||
DARZALEX (daratumumab)-SC based quadruplet regimen approved by the European Commission for patients with newly diagnosed multiple myeloma who are transplant-eligible |
Data Releases |
RYBREVANT (amivantamab-vmjw) plus LAZCLUZE (lazertinib) show statistically significant and clinically meaningful improvement in overall survival versus osimertinib1
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Johnson & Johnson to showcase strength of its broad hematology portfolio and pipeline at the 2024 American Society of Hematology Annual Meeting | ||
Icotrokinra delivered an industry-leading combination of significant skin clearance with demonstrated tolerability in a once daily pill in Phase 3 topline results | ||
Johnson & Johnson advances leadership in rheumatic disease innovation with 43 abstracts at ACR 2024 | ||
Shockwave Medical Unveils First Clinical Outcomes of New IVL Platform in Late-Breaking Presentation at VIVA 2024 | ||
TREMFYA (guselkumab) is the first and only IL-23 inhibitor to demonstrate robust results with a fully subcutaneous regimen in both induction and maintenance in Crohn's disease | ||
New SPECTREM study findings reveal TREMFYA (guselkumab) effectively clears overlooked and undertreated plaque psoriasis | ||
Johnson & Johnson highlights innovative neuropsychiatry portfolio and pipeline at Psych Congress | ||
Nipocalimab demonstrates sustained disease control in adolescents living with generalized myasthenia gravis in Phase 2/3 study | ||
Product Launch | MENTOR MemoryGel Enhance Breast Implant Receives FDA Approval for Largest Size Breast Implants for Reconstruction | |
Johnson & Johnson MedTech Receives FDA Approval for the VARIPULSE Pulsed Field Ablation Platform for the Treatment of Atrial Fibrillation2
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Other |
Johnson & Johnson Strengthens Neuroscience Leadership with Acquisition of Intra-Cellular Therapies, Inc.1
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