Does TERIPARATIDE Cause Incorrect product storage? 573 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 573 reports of Incorrect product storage have been filed in association with TERIPARATIDE (Bonsity). This represents 0.8% of all adverse event reports for TERIPARATIDE.
573
Reports of Incorrect product storage with TERIPARATIDE
0.8%
of all TERIPARATIDE reports
0
Deaths
25
Hospitalizations
How Dangerous Is Incorrect product storage From TERIPARATIDE?
Of the 573 reports, 25 (4.4%) required hospitalization.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TERIPARATIDE. However, 573 reports have been filed with the FAERS database.
What Other Side Effects Does TERIPARATIDE Cause?
Arthralgia (6,496)
Nausea (6,190)
Pain in extremity (6,012)
Dizziness (5,539)
Pain (5,077)
Fatigue (5,034)
Injection site bruising (4,405)
Muscle spasms (4,279)
Malaise (3,972)
Back pain (3,929)
What Other Drugs Cause Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
CYCLOSPORINE (203)
Which TERIPARATIDE Alternatives Have Lower Incorrect product storage Risk?
TERIPARATIDE vs TERIZIDONE
TERIPARATIDE vs TERLIPRESSIN
TERIPARATIDE vs TESAMORELIN
TERIPARATIDE vs TESTOSTERONE
TERIPARATIDE vs TESTOSTERONE CYPIONATE