🇺🇸 Kwells in United States

171 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. Platelet Count Decreased — 24 reports (14.04%)
  2. Pyrexia — 20 reports (11.7%)
  3. Renal Failure — 18 reports (10.53%)
  4. White Blood Cell Count Increased — 17 reports (9.94%)
  5. Overdose — 16 reports (9.36%)
  6. Red Blood Cell Count Decreased — 16 reports (9.36%)
  7. Blood Creatine Phosphokinase Increased — 15 reports (8.77%)
  8. Constipation — 15 reports (8.77%)
  9. Hyperhidrosis — 15 reports (8.77%)
  10. Hypertension — 15 reports (8.77%)

Source database →

Other Other approved in United States

Frequently asked questions

Is Kwells approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Kwells in United States?

Medical Corps, Israel Defense Force is the originator. The local marketing authorisation holder may differ — check the official source linked above.