Does BRIVARACETAM Cause Wrong technique in product usage process? 119 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 119 reports of Wrong technique in product usage process have been filed in association with BRIVARACETAM (Brivaracetam). This represents 2.0% of all adverse event reports for BRIVARACETAM.
119
Reports of Wrong technique in product usage process with BRIVARACETAM
2.0%
of all BRIVARACETAM reports
3
Deaths
37
Hospitalizations
How Dangerous Is Wrong technique in product usage process From BRIVARACETAM?
Of the 119 reports, 3 (2.5%) resulted in death, 37 (31.1%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRIVARACETAM. However, 119 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 technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which BRIVARACETAM Alternatives Have Lower Wrong technique in product usage process Risk?
BRIVARACETAM vs BRIVUDINE
BRIVARACETAM vs BRODALUMAB
BRIVARACETAM vs BROLUCIZUMAB
BRIVARACETAM vs BROLUCIZUMAB-DBLL
BRIVARACETAM vs BROMAZEPAM