Does CENOBAMATE Cause Wrong technique in product usage process? 268 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 268 reports of Wrong technique in product usage process have been filed in association with CENOBAMATE (Xcopri). This represents 4.8% of all adverse event reports for CENOBAMATE.
268
Reports of Wrong technique in product usage process with CENOBAMATE
4.8%
of all CENOBAMATE reports
1
Deaths
60
Hospitalizations
How Dangerous Is Wrong technique in product usage process From CENOBAMATE?
Of the 268 reports, 1 (0.4%) resulted in death, 60 (22.4%) required hospitalization, and 4 (1.5%) were considered life-threatening.
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 CENOBAMATE. However, 268 reports have been filed with the FAERS database.
What Other Side Effects Does CENOBAMATE Cause?
Seizure (1,544)
Product dose omission issue (1,229)
Fatigue (608)
Somnolence (588)
Dizziness (486)
Off label use (376)
Product use issue (364)
Fall (323)
Headache (301)
Feeling abnormal (237)
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 CENOBAMATE Alternatives Have Lower Wrong technique in product usage process Risk?
CENOBAMATE vs CEPHALEXIN
CENOBAMATE vs CERITINIB
CENOBAMATE vs CERLIPONASE ALFA
CENOBAMATE vs CERTICAN
CENOBAMATE vs CERTOLIZUMAB