Does ABALOPARATIDE Cause Product dose omission in error? 457 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 457 reports of Product dose omission in error have been filed in association with ABALOPARATIDE (Tymlos). This represents 2.0% of all adverse event reports for ABALOPARATIDE.
457
Reports of Product dose omission in error with ABALOPARATIDE
2.0%
of all ABALOPARATIDE reports
0
Deaths
12
Hospitalizations
How Dangerous Is Product dose omission in error From ABALOPARATIDE?
Of the 457 reports, 12 (2.6%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABALOPARATIDE. However, 457 reports have been filed with the FAERS database.
What Other Side Effects Does ABALOPARATIDE Cause?
Headache (4,048)
Nausea (3,134)
Dizziness (3,005)
Fatigue (2,637)
Heart rate increased (2,092)
Palpitations (1,730)
Arthralgia (1,711)
Bone pain (1,360)
Back pain (1,229)
Pain (1,191)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
RELUGOLIX (293)
Which ABALOPARATIDE Alternatives Have Lower Product dose omission in error Risk?
ABALOPARATIDE vs ABATACEPT
ABALOPARATIDE vs ABATACEPT SUBQ /ML
ABALOPARATIDE vs ABCIXIMAB
ABALOPARATIDE vs ABEMACICLIB
ABALOPARATIDE vs ABILIFY