Does BRIVARACETAM Cause Wrong product administered? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Wrong product administered have been filed in association with BRIVARACETAM (Brivaracetam). This represents 0.1% of all adverse event reports for BRIVARACETAM.
5
Reports of Wrong product administered with BRIVARACETAM
0.1%
of all BRIVARACETAM reports
1
Deaths
1
Hospitalizations
How Dangerous Is Wrong product administered From BRIVARACETAM?
Of the 5 reports, 1 (20.0%) resulted in death, 1 (20.0%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIVARACETAM. However, 5 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which BRIVARACETAM Alternatives Have Lower Wrong product administered Risk?
BRIVARACETAM vs BRIVUDINE
BRIVARACETAM vs BRODALUMAB
BRIVARACETAM vs BROLUCIZUMAB
BRIVARACETAM vs BROLUCIZUMAB-DBLL
BRIVARACETAM vs BROMAZEPAM