🇺🇸 Isobide in United States

87 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. Malignant Neoplasm Progression — 14 reports (16.09%)
  2. Hepatic Function Abnormal — 11 reports (12.64%)
  3. Diarrhoea — 10 reports (11.49%)
  4. Disease Progression — 9 reports (10.34%)
  5. Interstitial Lung Disease — 8 reports (9.2%)
  6. Pneumonia — 8 reports (9.2%)
  7. Lymphocyte Count Decreased — 7 reports (8.05%)
  8. Nausea — 7 reports (8.05%)
  9. Vomiting — 7 reports (8.05%)
  10. Dizziness — 6 reports (6.9%)

Source database →

Isobide in other countries

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

Other Cardiovascular approved in United States

Frequently asked questions

Is Isobide approved in United States?

Yes. FDA has authorised it.

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

Alvogen Korea is the originator. The local marketing authorisation holder may differ — check the official source linked above.