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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 Condition aggravated? 403 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 403 reports of Condition aggravated have been filed in association with ABALOPARATIDE (Tymlos). This represents 1.7% of all adverse event reports for ABALOPARATIDE.

403
Reports of Condition aggravated with ABALOPARATIDE
1.7%
of all ABALOPARATIDE reports
1
Deaths
19
Hospitalizations

How Dangerous Is Condition aggravated From ABALOPARATIDE?

Of the 403 reports, 1 (0.2%) resulted in death, 19 (4.7%) required hospitalization, and 1 (0.2%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ABALOPARATIDE. However, 403 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which ABALOPARATIDE Alternatives Have Lower Condition aggravated Risk?

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

Related Pages

ABALOPARATIDE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated ABALOPARATIDE Demographics