Does VIGABATRIN Cause Product dose omission issue? 304 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 304 reports of Product dose omission issue have been filed in association with VIGABATRIN (Vigabatrin). This represents 2.5% of all adverse event reports for VIGABATRIN.
304
Reports of Product dose omission issue with VIGABATRIN
2.5%
of all VIGABATRIN reports
0
Deaths
104
Hospitalizations
How Dangerous Is Product dose omission issue From VIGABATRIN?
Of the 304 reports, 104 (34.2%) required hospitalization, and 1 (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 VIGABATRIN. However, 304 reports have been filed with the FAERS database.
What Other Side Effects Does VIGABATRIN Cause?
Seizure (2,289)
Drug ineffective (1,212)
Drug dose omission (987)
Death (721)
Drug withdrawal convulsions (460)
Pneumonia (432)
Somnolence (427)
Vomiting (369)
Infantile spasms (257)
Off label use (248)
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 VIGABATRIN Alternatives Have Lower Product dose omission issue Risk?
VIGABATRIN vs VIIBRYD
VIGABATRIN vs VILANTEROL
VIGABATRIN vs VILANTEROL TRIFENATATE
VIGABATRIN vs VILAZODONE
VIGABATRIN vs VILDAGLIPTIN