🇺🇸 TERODILINE HYDROCHLORIDE in United States

30 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. Acute Pulmonary Oedema — 3 reports (10%)
  2. Alanine Aminotransferase Increased — 3 reports (10%)
  3. Blood Chloride Decreased — 3 reports (10%)
  4. Blood Creatinine Increased — 3 reports (10%)
  5. Blood Potassium Decreased — 3 reports (10%)
  6. Blood Urea Increased — 3 reports (10%)
  7. Cardiogenic Shock — 3 reports (10%)
  8. Dizziness Postural — 3 reports (10%)
  9. Gamma-Glutamyltransferase Increased — 3 reports (10%)
  10. Heart Rate Decreased — 3 reports (10%)

Source database →

TERODILINE 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 TERODILINE HYDROCHLORIDE approved in United States?

Yes. FDA has authorised it.

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

Marketing authorisation holder not available in our data.