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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 Prescribed underdose? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Prescribed underdose have been filed in association with RIPRETINIB (QINLOCK). This represents 0.5% of all adverse event reports for RIPRETINIB.

21
Reports of Prescribed underdose with RIPRETINIB
0.5%
of all RIPRETINIB reports
0
Deaths
3
Hospitalizations

How Dangerous Is Prescribed underdose From RIPRETINIB?

Of the 21 reports, 3 (14.3%) required hospitalization.

Is Prescribed underdose Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIPRETINIB. However, 21 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 Prescribed underdose?

NATALIZUMAB (2,162) SACUBITRIL\VALSARTAN (1,864) APIXABAN (1,469) ABATACEPT (1,192) PIMAVANSERIN (1,165) FINGOLIMOD (1,114) RITUXIMAB (1,067) METHOTREXATE (1,066) ADALIMUMAB (1,010) TOCILIZUMAB (1,002)

Which RIPRETINIB Alternatives Have Lower Prescribed underdose Risk?

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

Related Pages

RIPRETINIB Full Profile All Prescribed underdose Reports All Drugs Causing Prescribed underdose RIPRETINIB Demographics