🇺🇸 Calcitonin Gene-Related Peptide in United States

7 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. Apathy — 1 report (14.29%)
  2. Death — 1 report (14.29%)
  3. Depression — 1 report (14.29%)
  4. Insomnia — 1 report (14.29%)
  5. Migraine — 1 report (14.29%)
  6. Therapeutic Product Effect Incomplete — 1 report (14.29%)
  7. Therapeutic Response Decreased — 1 report (14.29%)

Source database →

Calcitonin Gene-Related Peptide 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 Calcitonin Gene-Related Peptide approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Calcitonin Gene-Related Peptide in United States?

Danish Headache Center is the originator. The local marketing authorisation holder may differ — check the official source linked above.