Does DEFERIPRONE Cause Product dose omission issue? 58 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 58 reports of Product dose omission issue have been filed in association with DEFERIPRONE (FERRIPROX). This represents 2.3% of all adverse event reports for DEFERIPRONE.
58
Reports of Product dose omission issue with DEFERIPRONE
2.3%
of all DEFERIPRONE reports
0
Deaths
24
Hospitalizations
How Dangerous Is Product dose omission issue From DEFERIPRONE?
Of the 58 reports, 24 (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 DEFERIPRONE. However, 58 reports have been filed with the FAERS database.
What Other Side Effects Does DEFERIPRONE Cause?
Off label use (916)
Death (190)
Sickle cell anaemia with crisis (167)
Nausea (135)
Agranulocytosis (126)
Vomiting (111)
Ill-defined disorder (106)
Fatigue (99)
Neutropenia (97)
Pyrexia (87)
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 DEFERIPRONE Alternatives Have Lower Product dose omission issue Risk?
DEFERIPRONE vs DEFEROXAMINE
DEFERIPRONE vs DEFIBROTIDE
DEFERIPRONE vs DEFLAZACORT
DEFERIPRONE vs DEGARELIX
DEFERIPRONE vs DELAFLOXACIN MEGLUMINE