Does BRIVARACETAM Cause Hyperammonaemia? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Hyperammonaemia have been filed in association with BRIVARACETAM (Brivaracetam). This represents 0.2% of all adverse event reports for BRIVARACETAM.
12
Reports of Hyperammonaemia with BRIVARACETAM
0.2%
of all BRIVARACETAM reports
0
Deaths
8
Hospitalizations
How Dangerous Is Hyperammonaemia From BRIVARACETAM?
Of the 12 reports, 8 (66.7%) required hospitalization, and 3 (25.0%) were considered life-threatening.
Is Hyperammonaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIVARACETAM. However, 12 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 Hyperammonaemia?
VALPROIC ACID (581)
VALPROATE (328)
FLUOROURACIL (263)
DIVALPROEX (256)
LEVETIRACETAM (192)
TACROLIMUS (181)
ACETAMINOPHEN (177)
OXALIPLATIN (160)
TOPIRAMATE (156)
GLYCEROL PHENYLBUTYRATE (147)
Which BRIVARACETAM Alternatives Have Lower Hyperammonaemia Risk?
BRIVARACETAM vs BRIVUDINE
BRIVARACETAM vs BRODALUMAB
BRIVARACETAM vs BROLUCIZUMAB
BRIVARACETAM vs BROLUCIZUMAB-DBLL
BRIVARACETAM vs BROMAZEPAM