Does ABALOPARATIDE Cause Product storage error? 285 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 285 reports of Product storage error have been filed in association with ABALOPARATIDE (Tymlos). This represents 1.2% of all adverse event reports for ABALOPARATIDE.
285
Reports of Product storage error with ABALOPARATIDE
1.2%
of all ABALOPARATIDE reports
1
Deaths
12
Hospitalizations
How Dangerous Is Product storage error From ABALOPARATIDE?
Of the 285 reports, 1 (0.4%) resulted in death, 12 (4.2%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABALOPARATIDE. However, 285 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which ABALOPARATIDE Alternatives Have Lower Product storage error Risk?
ABALOPARATIDE vs ABATACEPT
ABALOPARATIDE vs ABATACEPT SUBQ /ML
ABALOPARATIDE vs ABCIXIMAB
ABALOPARATIDE vs ABEMACICLIB
ABALOPARATIDE vs ABILIFY