🇺🇸 CHLOPHEDIANOL HYDROCHLORIDE in United States

24 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. Febrile Neutropenia — 8 reports (33.33%)
  2. Enterobacter Bacteraemia — 4 reports (16.67%)
  3. Clostridium Difficile Colitis — 2 reports (8.33%)
  4. Pneumonia — 2 reports (8.33%)
  5. Serotonin Syndrome — 2 reports (8.33%)
  6. Stevens-Johnson Syndrome — 2 reports (8.33%)
  7. Anaemia — 1 report (4.17%)
  8. Colitis Ischaemic — 1 report (4.17%)
  9. Intensive Care — 1 report (4.17%)
  10. Myocarditis — 1 report (4.17%)

Source database →

CHLOPHEDIANOL HYDROCHLORIDE 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 CHLOPHEDIANOL HYDROCHLORIDE approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for CHLOPHEDIANOL HYDROCHLORIDE in United States?

Marketing authorisation holder not available in our data.