Does REPOTRECTINIB Cause Adverse event? 11 Reports in FDA Database

Q: Does REPOTRECTINIB cause Adverse event?

11 reports of Adverse event have been filed with the FDA for REPOTRECTINIB, representing 5.9% of all REPOTRECTINIB adverse event reports.

Q: How dangerous is Adverse event from REPOTRECTINIB?

Of 11 reports, 1 (9.1%) resulted in death and 6 required hospitalization.

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Adverse event have been filed in association with REPOTRECTINIB (Augtyro). This represents 5.9% of all adverse event reports for REPOTRECTINIB.

Reports of Adverse event with REPOTRECTINIB

5.9%

of all REPOTRECTINIB reports

Deaths

Hospitalizations

How Dangerous Is Adverse event From REPOTRECTINIB?

Of the 11 reports, 1 (9.1%) resulted in death, 6 (54.5%) required hospitalization, and 2 (18.2%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REPOTRECTINIB. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does REPOTRECTINIB Cause?

Dizziness (32) Death (21) Nausea (12) Neuropathy peripheral (11) Off label use (10) Paraesthesia (10) Balance disorder (9) Pain (9) Hospitalisation (8) Muscular weakness (8)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which REPOTRECTINIB Alternatives Have Lower Adverse event Risk?

REPOTRECTINIB vs REQUIP REPOTRECTINIB vs RESLIZUMAB REPOTRECTINIB vs RESMETIROM REPOTRECTINIB vs RESTASIS REPOTRECTINIB vs RETINOL

REPOTRECTINIB Full Profile All Adverse event Reports All Drugs Causing Adverse event REPOTRECTINIB Demographics