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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 RIMEGEPANT Cause Unevaluable event? 73 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 73 reports of Unevaluable event have been filed in association with RIMEGEPANT (NURTEC ODT). This represents 0.8% of all adverse event reports for RIMEGEPANT.

73
Reports of Unevaluable event with RIMEGEPANT
0.8%
of all RIMEGEPANT reports
0
Deaths
1
Hospitalizations

How Dangerous Is Unevaluable event From RIMEGEPANT?

Of the 73 reports, 1 (1.4%) required hospitalization.

Is Unevaluable event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIMEGEPANT. However, 73 reports have been filed with the FAERS database.

What Other Side Effects Does RIMEGEPANT Cause?

Drug ineffective (3,624) Nausea (867) Therapeutic product effect incomplete (584) Migraine (447) Headache (439) Off label use (350) Dizziness (298) Vomiting (242) Feeling abnormal (232) Therapeutic product effect decreased (207)

What Other Drugs Cause Unevaluable event?

ADALIMUMAB (4,242) ETANERCEPT (3,902) LENALIDOMIDE (3,331) OXYCODONE (3,145) AMBRISENTAN (2,336) SODIUM OXYBATE (2,328) CARBIDOPA\LEVODOPA (1,632) DUPILUMAB (1,410) MORPHINE (1,161) ACETAMINOPHEN\HYDROCODONE (1,118)

Which RIMEGEPANT Alternatives Have Lower Unevaluable event Risk?

RIMEGEPANT vs RIOCIGUAT RIMEGEPANT vs RIPRETINIB RIMEGEPANT vs RISANKIZUMAB RIMEGEPANT vs RISANKIZUMAB-RZAA RIMEGEPANT vs RISDIPLAM

Related Pages

RIMEGEPANT Full Profile All Unevaluable event Reports All Drugs Causing Unevaluable event RIMEGEPANT Demographics