🇺🇸 PO Acetaminophen in United States

8 US adverse-event reports

Marketing authorisation

FDA

  • Status: approved

Safety signals — FAERS

Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.

Most-reported reactions

  1. Blood Pressure Increased — 1 report (12.5%)
  2. Chest X-Ray Abnormal — 1 report (12.5%)
  3. Chills — 1 report (12.5%)
  4. Dyspnoea — 1 report (12.5%)
  5. Heart Rate Increased — 1 report (12.5%)
  6. Infusion Related Reaction — 1 report (12.5%)
  7. Leukocytosis — 1 report (12.5%)
  8. Pyrexia — 1 report (12.5%)

Source database →

PO Acetaminophen in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is PO Acetaminophen approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for PO Acetaminophen in United States?

Corewell Health West is the originator. The local marketing authorisation holder may differ — check the official source linked above.