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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 RIPRETINIB Cause Therapy interrupted? 68 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Therapy interrupted have been filed in association with RIPRETINIB (QINLOCK). This represents 1.5% of all adverse event reports for RIPRETINIB.

68
Reports of Therapy interrupted with RIPRETINIB
1.5%
of all RIPRETINIB reports
2
Deaths
18
Hospitalizations

How Dangerous Is Therapy interrupted From RIPRETINIB?

Of the 68 reports, 2 (2.9%) resulted in death, 18 (26.5%) required hospitalization, and 1 (1.5%) were considered life-threatening.

Is Therapy interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIPRETINIB. However, 68 reports have been filed with the FAERS database.

What Other Side Effects Does RIPRETINIB Cause?

Fatigue (582) Alopecia (517) Extra dose administered (357) Death (356) Underdose (345) Nausea (292) Drug ineffective (291) Disease progression (290) Hospitalisation (280) Neoplasm progression (263)

What Other Drugs Cause Therapy interrupted?

ADALIMUMAB (5,755) ETANERCEPT (3,397) RELUGOLIX (3,251) CERTOLIZUMAB PEGOL (3,209) LENALIDOMIDE (2,724) UPADACITINIB (1,741) ABATACEPT (1,726) CLOZAPINE (1,722) AMIKACIN (1,283) TOFACITINIB (1,182)

Which RIPRETINIB Alternatives Have Lower Therapy interrupted Risk?

RIPRETINIB vs RISANKIZUMAB RIPRETINIB vs RISANKIZUMAB-RZAA RIPRETINIB vs RISDIPLAM RIPRETINIB vs RISEDRONATE RIPRETINIB vs RISEDRONIC ACID

Related Pages

RIPRETINIB Full Profile All Therapy interrupted Reports All Drugs Causing Therapy interrupted RIPRETINIB Demographics