Does RIMEGEPANT Cause Product prescribing issue? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product prescribing issue have been filed in association with RIMEGEPANT (NURTEC ODT). This represents 0.1% of all adverse event reports for RIMEGEPANT.
10
Reports of Product prescribing issue with RIMEGEPANT
0.1%
of all RIMEGEPANT reports
0
Deaths
6
Hospitalizations
How Dangerous Is Product prescribing issue From RIMEGEPANT?
Of the 10 reports, 6 (60.0%) required hospitalization.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIMEGEPANT. However, 10 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which RIMEGEPANT Alternatives Have Lower Product prescribing issue Risk?
RIMEGEPANT vs RIOCIGUAT
RIMEGEPANT vs RIPRETINIB
RIMEGEPANT vs RISANKIZUMAB
RIMEGEPANT vs RISANKIZUMAB-RZAA
RIMEGEPANT vs RISDIPLAM