Pfizer 8-K

EarningsGuidance reaffirmedLegal / investigation

Launched and acquired products drive growth despite steep Comirnaty and Paxlovid declines.

Filed 2026-05-05 07:01 ET

Summary

Q1 2026 results with FY2026 guidance reaffirmed. Revenue rose 5% reported and 2% operationally; growth from launched and acquired products was partly offset by lower COVID-19 product revenue. Pfizer also expects to start ≈20 key pivotal studies in 2026.

Key Figures

Metric Q1 2026 Q1 2025 Y/Y
Revenue $14.5B $13.7B 5%
Net income attributable to Pfizer Inc. common shareholders $2.69B $2.97B -9%
Adjusted income, non-GAAP $4.29B $5.24B -18%
Diluted EPS attributable to Pfizer Inc. common shareholders $0.47 $0.52 -10%
Adjusted diluted EPS, non-GAAP $0.75 $0.92 -18%
  • Operational revenue growth was 2%; excluding Comirnaty and Paxlovid, it was 7%. Launched and acquired products grew 22% operationally, while Comirnaty and Paxlovid fell 59% and 63% operationally, respectively.
  • Shareholder dividends were $2.4B, or $0.43 per share. No share repurchases have occurred in 2026; guidance assumes none, and $3.3B remains authorized.
  • Settlements with Dexcel Pharma, Hikma Pharmaceuticals and Cipla extend Vyndamax’s effective U.S. patent expiry to 6/1/2031, subject to other litigation. Pfizer now expects Vyndamax revenue to remain relatively stable from 2028 through mid-2031, rather than declining significantly beginning in 2029.

Guidance

All components of FY2026 guidance were reaffirmed. The outlook includes an anticipated ≈$1.5B unfavorable revenue impact from recent and expected generic and biosimilar competition.

Metric Period Guidance Prior Direction
Revenue (GAAP) FY2026 $59.5B-$62.5B — Reaffirmed
Selling, informational and administrative expenses (non-GAAP) FY2026 $12.5B-$13.5B — Reaffirmed
R&D expenses (non-GAAP) FY2026 $10.5B-$11.5B — Reaffirmed
Effective tax rate on adjusted income (non-GAAP) FY2026 ≈15.0% — Reaffirmed
Diluted EPS (non-GAAP) FY2026 $2.80-$3.00 — Reaffirmed

Investor Takeaways

  • Watch whether operational growth in launched and acquired products can offset continued COVID-19 product declines and the expected generic and biosimilar headwind.
  • Progress toward the planned start of ≈20 pivotal studies in 2026, alongside upcoming clinical and regulatory decisions, will indicate the pace of pipeline advancement.

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