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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 Underdose? 345 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 345 reports of Underdose have been filed in association with RIPRETINIB (QINLOCK). This represents 7.8% of all adverse event reports for RIPRETINIB.

345
Reports of Underdose with RIPRETINIB
7.8%
of all RIPRETINIB reports
19
Deaths
67
Hospitalizations

How Dangerous Is Underdose From RIPRETINIB?

Of the 345 reports, 19 (5.5%) resulted in death, 67 (19.4%) required hospitalization, and 1 (0.3%) were considered life-threatening.

Is Underdose Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIPRETINIB. However, 345 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) Nausea (292) Drug ineffective (291) Disease progression (290) Hospitalisation (280) Neoplasm progression (263) Constipation (249)

What Other Drugs Cause Underdose?

ADAPALENE (5,192) AVOBENZONE\OCTISALATE\OCTOCRYLENE (3,722) INSULIN LISPRO (3,156) ETANERCEPT (3,145) GALCANEZUMAB-GNLM (2,909) ENZALUTAMIDE (2,017) FLUTICASONE\SALMETEROL (1,600) ALBUTEROL (1,593) EXENATIDE (1,571) TROFINETIDE (1,540)

Which RIPRETINIB Alternatives Have Lower 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 Underdose Reports All Drugs Causing Underdose RIPRETINIB Demographics