04/14/2026 | Press release | Distributed by Public on 04/14/2026 05:35
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Q1
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||||||||||||||||||||
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($ in Millions, except EPS)
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2026
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2025
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% Change
|
|||||||||||||||||
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Reported Sales
|
|
$24,062
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$21,893
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9.9%
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||||||||||||||||
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Net Earnings
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$5,235
|
$10,999
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-52.4%
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|||||||||||||||||
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EPS (diluted)
|
$2.14
|
$4.54
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-52.9%
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Q1
|
|||||||||||||||||||
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Non-GAAP* ($ in Millions, except EPS)
|
2026
|
2025
|
% Change
|
|||||||||||||||||
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Operational Sales1,2
|
|
|
6.4%
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|||||||||||||||||
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Adjusted Operational Sales1,3
|
|
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5.3%
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|||||||||||||||||
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Adjusted Net Earnings1,4
|
$6,614
|
$6,706
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-1.4%
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Adjusted EPS (diluted)1,4
|
$2.70
|
$2.77
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-2.5%
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|||||||||||||||||
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Free Cash Flow5,6
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~$1,500
|
$3,379
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|
Q1
|
|
|
|
% Change
|
|
|||||||||||||||
|
($ in Millions)
|
2026
|
2025
|
Reported
|
Operational1,2
|
Currency
|
Adjusted
Operational1,3
|
||||||||||||||
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U.S.
|
$13,330
|
$12,305
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8.3%
|
8.3
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-
|
6.2
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||||||||||||||
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International
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10,732
|
9,588
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11.9
|
3.9
|
8.0
|
4.0
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||||||||||||||
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Worldwide
|
$24,062
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$21,893
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9.9%
|
6.4
|
3.5
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5.3
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|
Q1
|
|
|
|
% Change
|
|
|||||||||||||||
|
($ in Millions)
|
2026
|
2025
|
Reported
|
Operational1,2
|
Currency
|
Adjusted
Operational1,3
|
||||||||||||||
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Innovative Medicine
|
$15,426
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$13,873
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11.2%
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7.4
|
3.8
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5.6
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MedTech
|
8,636
|
8,020
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7.7
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4.6
|
3.1
|
4.7
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||||||||||||||
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Worldwide
|
$24,062
|
$21,893
|
9.9%
|
6.4
|
3.5
|
5.3
|
||||||||||||||
|
($ in Billions, except EPS)
|
April 2026
|
January 2026
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||||||
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Adjusted Operational Sales1,2
Change vs. Prior Year / Mid-point
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5.6% - 6.6% / 6.1%
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5.4% - 6.4% / 5.9%
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||||||
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Operational Sales2 / Mid-point
Change vs. Prior Year / Mid-point
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$99.7B - $100.7B / $100.2B
5.9% - 6.9% / 6.4%
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$99.5B - $100.5B / $100.0B
5.7% - 6.7% / 6.2%
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Estimated Reported Sales3/ Mid-point
Change vs. Prior Year / Mid-point
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$100.3B - $101.3B / $100.8B
6.5% - 7.5% / 7.0%
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$100.0B - $101.0B / $100.5B
6.2% - 7.2% / 6.7%
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Adjusted Operational EPS (Diluted)2,4 / Mid-point
Change vs. Prior Year / Mid-point
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$11.30 - $11.50 / $11.40
4.7% - 6.7% / 5.7%
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$11.28 - $11.48 / $11.38
4.5% - 6.5% / 5.5%
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Adjusted EPS (Diluted)3,4 / Mid-point
Change vs. Prior Year / Mid-point
|
$11.45 - $11.65 / $11.55
6.1% - 8.1% / 7.1%
|
$11.43 - $11.63 / $11.53
5.9% - 7.9% / 6.9%
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Regulatory
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Johnson & Johnson Announces FDA Approval of TECNIS PureSee Intraocular Lens, a Breakthrough Solution for U.S. Cataract Patients
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Johnson & Johnson Announces U.S. FDA Approval of TECVAYLI plus DARZALEX FASPRO for Relapsed/Refractory Multiple Myeloma, Offering a Potential New Standard of Care as Early as Second Line
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Johnson & Johnson therapy nipocalimab granted U.S. FDA Fast Track designation in systemic lupus erythematosus (SLE)
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Johnson & Johnson seeks FDA approval of IMAAVY (nipocalimab-aahu) as the first-ever FDA-approved treatment for warm autoimmune hemolytic anemia (wAIHA)
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RYBREVANT FASPRO (amivantamab and hyaluronidase-lpuj) receives U.S. FDA Breakthrough Therapy Designation for patients with advanced head and neck cancer
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FDA approves RYBREVANT FASPRO (amivantamab and hyaluronidase-lpuj) as the only EGFR-targeted therapy that can be administered once a month
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DARZALEX FASPRO-based quadruplet regimen approved in the U.S. for newly diagnosed patients with multiple myeloma who are transplant ineligible
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Data Releases
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Johnson & Johnson Highlights Favorable 12-Month Interim Results for the VARIPULSE Platform at EHRA 20261
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Johnson & Johnson Showcases New Clinical Data for TECNIS PureSee IOL at ASCRS 2026 Demonstrating Excellent Contrast Sensitivity and Extended Range of Vision1
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STEMI DTU Randomized Control Trial Demonstrates for the First Time that a Combination of Delayed Reperfusion and Left Ventricular Unloading Does Not Increase Myocardial Infarct Size
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ICOTYDE (icotrokinra) one-year results confirm lasting skin clearance and favorable safety profile in once-daily pill for plaque psoriasis
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Johnson & Johnson highlights promising first-in-human Erda-iDRS (formerly TAR-210) results in intermediate-risk non-muscle-invasive bladder cancer
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Early study results from Johnson & Johnson show promising antitumor activity with combination of pasritamig and docetaxel in advanced prostate cancer
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TREMFYA (guselkumab) long-term data show sustained clinical and endoscopic remission in ulcerative colitis through 3 years
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RYBREVANT FASPRO (amivantamab and hyaluronidase-lpuj) plus immunotherapy shows strong clinical benefit with 56 percent overall response rate in first-line recurrent or metastatic head and neck cancer
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Johnson & Johnson Presents Early Outcomes from the OMNY-AF Pilot Study at 2026 AF Symposium
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Real-world head-to-head analysis shows 51% reduction in risk of death for patients with metastatic castration-sensitive prostate cancer treated with ERLEADA (apalutamide) versus darolutamide without docetaxel through 24 months
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Product Launch
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Johnson & Johnson Advances Pulsed Field Ablation Portfolio with the Launch of VARIPULSE Pro in Europe1
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FDA approval of ICOTYDE (icotrokinra) ushers in new era for first-line systemic treatment of plaque psoriasis with a targeted oral peptide
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Other
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Johnson & Johnson Expands U.S. Footprint with more than $1 Billion Investment in Next Generation Cell Therapy Manufacturing Facility in Pennsylvania
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