Does BRIVARACETAM Cause Product dose omission? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Product dose omission have been filed in association with BRIVARACETAM (Brivaracetam). This represents 0.6% of all adverse event reports for BRIVARACETAM.
36
Reports of Product dose omission with BRIVARACETAM
0.6%
of all BRIVARACETAM reports
0
Deaths
17
Hospitalizations
How Dangerous Is Product dose omission From BRIVARACETAM?
Of the 36 reports, 17 (47.2%) required hospitalization, and 1 (2.8%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIVARACETAM. However, 36 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which BRIVARACETAM Alternatives Have Lower Product dose omission Risk?
BRIVARACETAM vs BRIVUDINE
BRIVARACETAM vs BRODALUMAB
BRIVARACETAM vs BROLUCIZUMAB
BRIVARACETAM vs BROLUCIZUMAB-DBLL
BRIVARACETAM vs BROMAZEPAM