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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 DAUNORUBICIN Cause Hypofibrinogenaemia? 186 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 186 reports of Hypofibrinogenaemia have been filed in association with DAUNORUBICIN (Daunorubicin Hydrochloride). This represents 1.9% of all adverse event reports for DAUNORUBICIN.

186
Reports of Hypofibrinogenaemia with DAUNORUBICIN
1.9%
of all DAUNORUBICIN reports
0
Deaths
48
Hospitalizations

How Dangerous Is Hypofibrinogenaemia From DAUNORUBICIN?

Of the 186 reports, 48 (25.8%) required hospitalization, and 4 (2.2%) were considered life-threatening.

Is Hypofibrinogenaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DAUNORUBICIN. However, 186 reports have been filed with the FAERS database.

What Other Side Effects Does DAUNORUBICIN Cause?

Febrile neutropenia (1,311) Pyrexia (645) Neutropenia (631) Sepsis (515) Off label use (462) Pneumonia (402) Bacterial infection (400) Drug ineffective (375) Septic shock (363) Thrombocytopenia (347)

What Other Drugs Cause Hypofibrinogenaemia?

METHOTREXATE (297) PEGASPARGASE (296) VINCRISTINE (295) CYTARABINE (177) DEXAMETHASONE (174) HYDROCORTISONE (126) PREDNISONE (124) TOCILIZUMAB (121) PREDNISOLONE (117) TIGECYCLINE (88)

Which DAUNORUBICIN Alternatives Have Lower Hypofibrinogenaemia Risk?

DAUNORUBICIN vs DAXIBOTULINUMTOXIN A-LANM DAUNORUBICIN vs DAYTRANA DAUNORUBICIN vs DECITABINE DAUNORUBICIN vs DEFERASIROX DAUNORUBICIN vs DEFERIPRONE

Related Pages

DAUNORUBICIN Full Profile All Hypofibrinogenaemia Reports All Drugs Causing Hypofibrinogenaemia DAUNORUBICIN Demographics