Does GANAXOLONE Cause Product dose omission issue? 84 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 84 reports of Product dose omission issue have been filed in association with GANAXOLONE (ZTALMY). This represents 16.4% of all adverse event reports for GANAXOLONE.
84
Reports of Product dose omission issue with GANAXOLONE
16.4%
of all GANAXOLONE reports
0
Deaths
9
Hospitalizations
How Dangerous Is Product dose omission issue From GANAXOLONE?
Of the 84 reports, 9 (10.7%) 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 GANAXOLONE. However, 84 reports have been filed with the FAERS database.
What Other Side Effects Does GANAXOLONE Cause?
Seizure (155)
Drug ineffective (79)
Change in seizure presentation (43)
Somnolence (38)
Pneumonia (24)
Vomiting (19)
Illness (14)
Off label use (12)
Fatigue (11)
Weight decreased (11)
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 GANAXOLONE Alternatives Have Lower Product dose omission issue Risk?
GANAXOLONE vs GANCICLOVIR
GANAXOLONE vs GANIRELIX
GANAXOLONE vs GATIFLOXACIN
GANAXOLONE vs GEFITINIB
GANAXOLONE vs GELATIN