Does BRIVARACETAM Cause Product administration interrupted? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product administration interrupted have been filed in association with BRIVARACETAM (Brivaracetam). This represents 0.1% of all adverse event reports for BRIVARACETAM.
6
Reports of Product administration interrupted with BRIVARACETAM
0.1%
of all BRIVARACETAM reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration interrupted From BRIVARACETAM?
Of the 6 reports, 2 (33.3%) required hospitalization.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIVARACETAM. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does BRIVARACETAM Cause?
Seizure (2,411)
Off label use (851)
Drug ineffective (695)
Fatigue (395)
Therapy interrupted (392)
Overdose (372)
Product availability issue (324)
Dizziness (322)
Somnolence (306)
Generalised tonic-clonic seizure (255)
What Other Drugs Cause Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which BRIVARACETAM Alternatives Have Lower Product administration interrupted Risk?
BRIVARACETAM vs BRIVUDINE
BRIVARACETAM vs BRODALUMAB
BRIVARACETAM vs BROLUCIZUMAB
BRIVARACETAM vs BROLUCIZUMAB-DBLL
BRIVARACETAM vs BROMAZEPAM