Does TERIPARATIDE Cause Incorrect product administration duration? 274 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 274 reports of Incorrect product administration duration have been filed in association with TERIPARATIDE (Bonsity). This represents 0.4% of all adverse event reports for TERIPARATIDE.
274
Reports of Incorrect product administration duration with TERIPARATIDE
0.4%
of all TERIPARATIDE reports
5
Deaths
68
Hospitalizations
How Dangerous Is Incorrect product administration duration From TERIPARATIDE?
Of the 274 reports, 5 (1.8%) resulted in death, 68 (24.8%) required hospitalization, and 3 (1.1%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TERIPARATIDE. However, 274 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 administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which TERIPARATIDE Alternatives Have Lower Incorrect product administration duration Risk?
TERIPARATIDE vs TERIZIDONE
TERIPARATIDE vs TERLIPRESSIN
TERIPARATIDE vs TESAMORELIN
TERIPARATIDE vs TESTOSTERONE
TERIPARATIDE vs TESTOSTERONE CYPIONATE