Does TERIPARATIDE Cause Recalled product? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Recalled product have been filed in association with TERIPARATIDE (Bonsity). This represents 0.0% of all adverse event reports for TERIPARATIDE.
12
Reports of Recalled product with TERIPARATIDE
0.0%
of all TERIPARATIDE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Recalled product From TERIPARATIDE?
Of the 12 reports, 4 (33.3%) required hospitalization, and 1 (8.3%) were considered life-threatening.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TERIPARATIDE. However, 12 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 Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which TERIPARATIDE Alternatives Have Lower Recalled product Risk?
TERIPARATIDE vs TERIZIDONE
TERIPARATIDE vs TERLIPRESSIN
TERIPARATIDE vs TESAMORELIN
TERIPARATIDE vs TESTOSTERONE
TERIPARATIDE vs TESTOSTERONE CYPIONATE