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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 PONATINIB Cause Condition aggravated? 57 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Condition aggravated have been filed in association with PONATINIB (Iclusig). This represents 0.6% of all adverse event reports for PONATINIB.

57
Reports of Condition aggravated with PONATINIB
0.6%
of all PONATINIB reports
11
Deaths
34
Hospitalizations

How Dangerous Is Condition aggravated From PONATINIB?

Of the 57 reports, 11 (19.3%) resulted in death, 34 (59.6%) required hospitalization, and 12 (21.1%) 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 PONATINIB. However, 57 reports have been filed with the FAERS database.

What Other Side Effects Does PONATINIB Cause?

Death (1,735) Off label use (1,071) Product dose omission issue (817) Fatigue (687) Rash (639) Headache (553) Pyrexia (542) Nausea (466) Hospitalisation (459) Constipation (435)

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 PONATINIB Alternatives Have Lower Condition aggravated Risk?

PONATINIB vs PONATINIB\PONATINIB PONATINIB vs PONESIMOD PONATINIB vs PORACTANT ALFA PONATINIB vs PORFIMER PONATINIB vs POSACONAZOLE

Related Pages

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