🇺🇸 Sublocade in United States

3,751 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. Drug Withdrawal Syndrome — 1,076 reports (28.69%)
  2. Injection Site Pain — 770 reports (20.53%)
  3. Drug Dependence — 378 reports (10.08%)
  4. Inappropriate Schedule Of Product Administration — 308 reports (8.21%)
  5. Injection Site Erythema — 273 reports (7.28%)
  6. Drug Abuse — 237 reports (6.32%)
  7. Nausea — 224 reports (5.97%)
  8. Wrong Technique In Product Usage Process — 173 reports (4.61%)
  9. Euphoric Mood — 160 reports (4.27%)
  10. Injection Site Infection — 152 reports (4.05%)

Source database →

Other Other approved in United States

Frequently asked questions

Is Sublocade approved in United States?

Yes. FDA has authorised it.

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

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