Does RIMEGEPANT Cause Product administration error? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product administration error have been filed in association with RIMEGEPANT (NURTEC ODT). This represents 0.1% of all adverse event reports for RIMEGEPANT.
13
Reports of Product administration error with RIMEGEPANT
0.1%
of all RIMEGEPANT reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration error From RIMEGEPANT?
Of the 13 reports, 1 (7.7%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIMEGEPANT. However, 13 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which RIMEGEPANT Alternatives Have Lower Product administration error Risk?
RIMEGEPANT vs RIOCIGUAT
RIMEGEPANT vs RIPRETINIB
RIMEGEPANT vs RISANKIZUMAB
RIMEGEPANT vs RISANKIZUMAB-RZAA
RIMEGEPANT vs RISDIPLAM