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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 AFATINIB Cause Intentional product use issue? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Intentional product use issue have been filed in association with AFATINIB (Gilotrif). This represents 0.3% of all adverse event reports for AFATINIB.

15
Reports of Intentional product use issue with AFATINIB
0.3%
of all AFATINIB reports
0
Deaths
2
Hospitalizations

How Dangerous Is Intentional product use issue From AFATINIB?

Of the 15 reports, 2 (13.3%) required hospitalization.

Is Intentional product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AFATINIB. However, 15 reports have been filed with the FAERS database.

What Other Side Effects Does AFATINIB Cause?

Diarrhoea (2,001) Malignant neoplasm progression (1,622) Rash (808) Stomatitis (468) Death (443) Nausea (430) Decreased appetite (412) Vomiting (381) Paronychia (344) Dehydration (323)

What Other Drugs Cause Intentional product use issue?

INFLIXIMAB (11,028) RITUXIMAB (9,602) INFLIXIMAB-DYYB (7,549) TOCILIZUMAB (5,078) METHOTREXATE (4,087) PREDNISONE (3,961) ABATACEPT (3,693) ADALIMUMAB (3,557) NIVOLUMAB (3,297) LEFLUNOMIDE (3,280)

Which AFATINIB Alternatives Have Lower Intentional product use issue Risk?

AFATINIB vs AFINITOR AFATINIB vs AFLIBERCEPT AFATINIB vs AGALSIDASE ALFA AFATINIB vs AGALSIDASE BETA AFATINIB vs AGOMELATINE

Related Pages

AFATINIB Full Profile All Intentional product use issue Reports All Drugs Causing Intentional product use issue AFATINIB Demographics