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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 Condition aggravated? 26 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Condition aggravated have been filed in association with DEFERIPRONE (FERRIPROX). This represents 1.1% of all adverse event reports for DEFERIPRONE.

26
Reports of Condition aggravated with DEFERIPRONE
1.1%
of all DEFERIPRONE reports
3
Deaths
13
Hospitalizations

How Dangerous Is Condition aggravated From DEFERIPRONE?

Of the 26 reports, 3 (11.5%) resulted in death, 13 (50.0%) required hospitalization, and 5 (19.2%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEFERIPRONE. However, 26 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which DEFERIPRONE Alternatives Have Lower Condition aggravated Risk?

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

Related Pages

DEFERIPRONE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated DEFERIPRONE Demographics