Safety
Teriparatide
Adverse-event report summary for Teriparatide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 6,936
- Reports flagged serious
- 4,925
“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
- Nausea518 reports
- Fall508 reports
- Dizziness499 reports
- Back Pain475 reports
- Fatigue473 reports
- Device Malfunction443 reports
- Arthralgia433 reports
- Pain In Extremity422 reports
- Product Dose Omission Issue402 reports
- Pain384 reports
- Headache363 reports
- Device Operational Issue360 reports
- Malaise296 reports
- Asthenia276 reports
- Dyspnoea237 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.