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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 Device defective? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device defective have been filed in association with ABALOPARATIDE (Tymlos). This represents 0.0% of all adverse event reports for ABALOPARATIDE.

5
Reports of Device defective with ABALOPARATIDE
0.0%
of all ABALOPARATIDE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device defective From ABALOPARATIDE?

Of the 5 reports.

Is Device defective Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ABALOPARATIDE. However, 5 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 Device defective?

SOMATROPIN (1,719) USTEKINUMAB (1,071) SECUKINUMAB (666) GUSELKUMAB (574) GOLIMUMAB (539) ABATACEPT (458) ALBUTEROL (445) TOCILIZUMAB (400) INSULIN GLARGINE (397) EXENATIDE (387)

Which ABALOPARATIDE Alternatives Have Lower Device defective Risk?

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

Related Pages

ABALOPARATIDE Full Profile All Device defective Reports All Drugs Causing Device defective ABALOPARATIDE Demographics