Does ABALOPARATIDE Cause Product use issue? 139 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 139 reports of Product use issue have been filed in association with ABALOPARATIDE (Tymlos). This represents 0.6% of all adverse event reports for ABALOPARATIDE.
139
Reports of Product use issue with ABALOPARATIDE
0.6%
of all ABALOPARATIDE reports
0
Deaths
8
Hospitalizations
How Dangerous Is Product use issue From ABALOPARATIDE?
Of the 139 reports, 8 (5.8%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABALOPARATIDE. However, 139 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)