Does GILTERITINIB Cause Condition aggravated? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Condition aggravated have been filed in association with GILTERITINIB (Xospata). This represents 1.3% of all adverse event reports for GILTERITINIB.
49
Reports of Condition aggravated with GILTERITINIB
1.3%
of all GILTERITINIB reports
16
Deaths
23
Hospitalizations
How Dangerous Is Condition aggravated From GILTERITINIB?
Of the 49 reports, 16 (32.7%) resulted in death, 23 (46.9%) required hospitalization, and 1 (2.0%) 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 GILTERITINIB. However, 49 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 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 GILTERITINIB Alternatives Have Lower Condition aggravated Risk?
GILTERITINIB vs GIMERACIL\OTERACIL\TEGAFUR
GILTERITINIB vs GINKGO
GILTERITINIB vs GIVINOSTAT
GILTERITINIB vs GIVOSIRAN
GILTERITINIB vs GLASDEGIB