Does ABALOPARATIDE Cause Product use complaint? 224 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 224 reports of Product use complaint have been filed in association with ABALOPARATIDE (Tymlos). This represents 1.0% of all adverse event reports for ABALOPARATIDE.
224
Reports of Product use complaint with ABALOPARATIDE
1.0%
of all ABALOPARATIDE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product use complaint From ABALOPARATIDE?
Of the 224 reports, 5 (2.2%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABALOPARATIDE. However, 224 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 use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
DIMETHICONE\LOPERAMIDE (201)
Which ABALOPARATIDE Alternatives Have Lower Product use complaint Risk?
ABALOPARATIDE vs ABATACEPT
ABALOPARATIDE vs ABATACEPT SUBQ /ML
ABALOPARATIDE vs ABCIXIMAB
ABALOPARATIDE vs ABEMACICLIB
ABALOPARATIDE vs ABILIFY