Does STIRIPENTOL Cause Product dose omission issue? 157 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 157 reports of Product dose omission issue have been filed in association with STIRIPENTOL. This represents 11.6% of all adverse event reports for STIRIPENTOL.
157
Reports of Product dose omission issue with STIRIPENTOL
11.6%
of all STIRIPENTOL reports
3
Deaths
65
Hospitalizations
How Dangerous Is Product dose omission issue From STIRIPENTOL?
Of the 157 reports, 3 (1.9%) resulted in death, 65 (41.4%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for STIRIPENTOL. However, 157 reports have been filed with the FAERS database.
What Other Side Effects Does STIRIPENTOL Cause?
Seizure (586)
Product use in unapproved indication (343)
Drug ineffective (193)
Decreased appetite (147)
Somnolence (139)
Product preparation issue (129)
Off label use (107)
Fatigue (95)
Hospitalisation (63)
Pyrexia (61)
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 STIRIPENTOL Alternatives Have Lower Product dose omission issue Risk?
STIRIPENTOL vs STIVARGA
STIRIPENTOL vs STRATTERA
STIRIPENTOL vs STREPTOCOCCUS PNEUMONIAE TYPE 1 CAPSULAR POLYSACCHARIDE DIPHTHERIA CRM197 PROTEIN CONJUGATE ANTIGEN\STREPTOCOCCUS PNEUMONIAE TYPE 14 CAPSULAR POLYSACCHARIDE DIPHTHERIA CRM197 PROTEIN CONJUGATE ANTIGEN\STREPTOCOCCUS PNEUMONIAE TYPE 18C CAPSULAR POLYSACCHARIDE DIPHTHERIA CRM197 PROTEIN CONJUGATE ANTIGEN\STREPTOCOCCUS PNEUMONIAE TYPE 19A CAPSULAR POLYSACCHARIDE DIPHTHERIA CRM197 PROTEIN CONJUGATE ANTIGEN\STREPTOCOCCUS PNEUMONIAE TYPE 19F CAPSULAR POLYSACCHARIDE DIPHTHERIA CRM197 PROTEIN CONJUGATE A
STIRIPENTOL vs STREPTOMYCIN
STIRIPENTOL vs STREPTOMYCIN\STREPTOMYCIN