Safety
Teriparatide
Adverse-event report summary for Teriparatide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 7,246
- Reports flagged serious
- 5,114
“Serious” is FAERS’s own report-level flag (e.g. death, hospitalization, or another outcome the reporter marked as serious) and does not indicate a verified or compound-caused outcome.
Most frequently reported reactions
- Nausea535 reports
- Fall526 reports
- Dizziness525 reports
- Fatigue491 reports
- Back Pain482 reports
- Arthralgia459 reports
- Device Malfunction444 reports
- Pain In Extremity434 reports
- Product Dose Omission Issue422 reports
- Pain401 reports
- Headache388 reports
- Device Operational Issue360 reports
- Malaise310 reports
- Asthenia283 reports
- Dyspnoea247 reports
Counts reflect the most-reported reaction terms (MedDRA preferred terms) associated with reports naming this compound. A single report can list multiple reactions, so reaction counts need not sum to the total number of reports.