Does GILTERITINIB Cause Subdural haematoma? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Subdural haematoma have been filed in association with GILTERITINIB (Xospata). This represents 0.6% of all adverse event reports for GILTERITINIB.
22
Reports of Subdural haematoma with GILTERITINIB
0.6%
of all GILTERITINIB reports
9
Deaths
11
Hospitalizations
How Dangerous Is Subdural haematoma From GILTERITINIB?
Of the 22 reports, 9 (40.9%) resulted in death, 11 (50.0%) required hospitalization, and 6 (27.3%) were considered life-threatening.
Is Subdural haematoma Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GILTERITINIB. However, 22 reports have been filed with the FAERS database.
What Other Side Effects Does GILTERITINIB Cause?
Acute myeloid leukaemia (366)
Febrile neutropenia (346)
Off label use (334)
Platelet count decreased (327)
Pneumonia (302)
Myelosuppression (300)
Pyrexia (281)
Death (206)
Product use issue (189)
Hepatic function abnormal (181)
What Other Drugs Cause Subdural haematoma?
RIVAROXABAN (1,423)
ASPIRIN (1,181)
APIXABAN (1,025)
WARFARIN (1,012)
CLOPIDOGREL BISULFATE (809)
DABIGATRAN ETEXILATE (648)
IBRUTINIB (342)
HEPARIN (201)
ENOXAPARIN (156)
CYCLOPHOSPHAMIDE (146)
Which GILTERITINIB Alternatives Have Lower Subdural haematoma Risk?
GILTERITINIB vs GIMERACIL\OTERACIL\TEGAFUR
GILTERITINIB vs GINKGO
GILTERITINIB vs GIVINOSTAT
GILTERITINIB vs GIVOSIRAN
GILTERITINIB vs GLASDEGIB