🇺🇸 naltrexone implant in United States

12 US adverse-event reports

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.

• Window: 28 March 2025 – 28 March 2026
• Total reports: 12

Most-reported reactions

1. Feeling Abnormal — 2 reports (16.67%)
2. Nausea — 2 reports (16.67%)
3. Alcohol Abuse — 1 report (8.33%)
4. Angina Pectoris — 1 report (8.33%)
5. Completed Suicide — 1 report (8.33%)
6. Delusion — 1 report (8.33%)
7. Dependence — 1 report (8.33%)
8. Drug Abuse — 1 report (8.33%)
9. Drug Withdrawal Syndrome — 1 report (8.33%)
10. Dysphagia — 1 report (8.33%)

Source database →

Frequently asked questions

Is naltrexone implant approved in United States?

naltrexone implant does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for naltrexone implant in United States?

Go Medical Industries Pty Ltd is the originator. The local marketing authorisation holder may differ — check the official source linked above.