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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 Intentional dose omission? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Intentional dose omission have been filed in association with RIPRETINIB (QINLOCK). This represents 0.3% of all adverse event reports for RIPRETINIB.

11
Reports of Intentional dose omission with RIPRETINIB
0.3%
of all RIPRETINIB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Intentional dose omission From RIPRETINIB?

Of the 11 reports.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIPRETINIB. However, 11 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 Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which RIPRETINIB Alternatives Have Lower Intentional dose omission Risk?

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

Related Pages

RIPRETINIB Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission RIPRETINIB Demographics