Does BRIVARACETAM Cause Product dose omission in error? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product dose omission in error have been filed in association with BRIVARACETAM (Brivaracetam). This represents 0.2% of all adverse event reports for BRIVARACETAM.
9
Reports of Product dose omission in error with BRIVARACETAM
0.2%
of all BRIVARACETAM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission in error From BRIVARACETAM?
Of the 9 reports, 1 (11.1%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIVARACETAM. However, 9 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 in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which BRIVARACETAM Alternatives Have Lower Product dose omission in error Risk?
BRIVARACETAM vs BRIVUDINE
BRIVARACETAM vs BRODALUMAB
BRIVARACETAM vs BROLUCIZUMAB
BRIVARACETAM vs BROLUCIZUMAB-DBLL
BRIVARACETAM vs BROMAZEPAM