Does CENOBAMATE Cause Product dose omission issue? 1,229 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,229 reports of Product dose omission issue have been filed in association with CENOBAMATE (Xcopri). This represents 21.8% of all adverse event reports for CENOBAMATE.
1,229
Reports of Product dose omission issue with CENOBAMATE
21.8%
of all CENOBAMATE reports
9
Deaths
175
Hospitalizations
How Dangerous Is Product dose omission issue From CENOBAMATE?
Of the 1,229 reports, 9 (0.7%) resulted in death, 175 (14.2%) required hospitalization, and 4 (0.3%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CENOBAMATE. However, 1,229 reports have been filed with the FAERS database.
What Other Side Effects Does CENOBAMATE Cause?
Seizure (1,544)
Fatigue (608)
Somnolence (588)
Dizziness (486)
Off label use (376)
Product use issue (364)
Fall (323)
Headache (301)
Wrong technique in product usage process (268)
Feeling abnormal (237)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which CENOBAMATE Alternatives Have Lower Product dose omission issue Risk?
CENOBAMATE vs CEPHALEXIN
CENOBAMATE vs CERITINIB
CENOBAMATE vs CERLIPONASE ALFA
CENOBAMATE vs CERTICAN
CENOBAMATE vs CERTOLIZUMAB