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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ABALOPARATIDE Cause Product complaint? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Product complaint have been filed in association with ABALOPARATIDE (Tymlos). This represents 0.1% of all adverse event reports for ABALOPARATIDE.

15
Reports of Product complaint with ABALOPARATIDE
0.1%
of all ABALOPARATIDE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product complaint From ABALOPARATIDE?

Of the 15 reports.

Is Product complaint Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ABALOPARATIDE. However, 15 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 complaint?

FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417) ALBUTEROL (2,291) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826) FLUTICASONE\SALMETEROL (1,601) MEPOLIZUMAB (1,296) FLUTICASONE (1,112) UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108) BELIMUMAB (1,079) SUMATRIPTAN (718) NICOTINE (700)

Which ABALOPARATIDE Alternatives Have Lower Product complaint Risk?

ABALOPARATIDE vs ABATACEPT ABALOPARATIDE vs ABATACEPT SUBQ /ML ABALOPARATIDE vs ABCIXIMAB ABALOPARATIDE vs ABEMACICLIB ABALOPARATIDE vs ABILIFY

Related Pages

ABALOPARATIDE Full Profile All Product complaint Reports All Drugs Causing Product complaint ABALOPARATIDE Demographics