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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DEFERIPRONE Cause Intentional dose omission? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Intentional dose omission have been filed in association with DEFERIPRONE (FERRIPROX). This represents 0.2% of all adverse event reports for DEFERIPRONE.

5
Reports of Intentional dose omission with DEFERIPRONE
0.2%
of all DEFERIPRONE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Intentional dose omission From DEFERIPRONE?

Of the 5 reports.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEFERIPRONE. However, 5 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 Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which DEFERIPRONE Alternatives Have Lower Intentional dose omission Risk?

DEFERIPRONE vs DEFEROXAMINE DEFERIPRONE vs DEFIBROTIDE DEFERIPRONE vs DEFLAZACORT DEFERIPRONE vs DEGARELIX DEFERIPRONE vs DELAFLOXACIN MEGLUMINE

Related Pages

DEFERIPRONE Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission DEFERIPRONE Demographics