Does GIVINOSTAT Cause Product dose omission issue? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product dose omission issue have been filed in association with GIVINOSTAT (DUVYZAT). This represents 4.9% of all adverse event reports for GIVINOSTAT.
13
Reports of Product dose omission issue with GIVINOSTAT
4.9%
of all GIVINOSTAT reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission issue From GIVINOSTAT?
Of the 13 reports, 3 (23.1%) 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 GIVINOSTAT. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does GIVINOSTAT Cause?
Platelet count decreased (88)
Diarrhoea (48)
Blood triglycerides increased (37)
Nausea (25)
Thrombocytopenia (25)
Abdominal discomfort (24)
Vomiting (24)
Abdominal pain upper (14)
Off label use (13)
Contusion (12)
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 GIVINOSTAT Alternatives Have Lower Product dose omission issue Risk?
GIVINOSTAT vs GIVOSIRAN
GIVINOSTAT vs GLASDEGIB
GIVINOSTAT vs GLATIRAMER
GIVINOSTAT vs GLECAPREVIR\PIBRENTASVIR
GIVINOSTAT vs GLEEVEC