Does SACITUZUMAB GOVITECAN Cause Haemoglobin abnormal? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Haemoglobin abnormal have been filed in association with SACITUZUMAB GOVITECAN (TRODELVY). This represents 1.0% of all adverse event reports for SACITUZUMAB GOVITECAN.
12
Reports of Haemoglobin abnormal with SACITUZUMAB GOVITECAN
1.0%
of all SACITUZUMAB GOVITECAN reports
5
Deaths
10
Hospitalizations
How Dangerous Is Haemoglobin abnormal From SACITUZUMAB GOVITECAN?
Of the 12 reports, 5 (41.7%) resulted in death, 10 (83.3%) required hospitalization.
Is Haemoglobin abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SACITUZUMAB GOVITECAN. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does SACITUZUMAB GOVITECAN Cause?
Disease progression (389)
Diarrhoea (184)
Death (182)
Inappropriate schedule of product administration (147)
Neutropenia (128)
Off label use (111)
Fatigue (109)
Febrile neutropenia (92)
Asthenia (90)
Weight decreased (89)
What Other Drugs Cause Haemoglobin abnormal?
RUXOLITINIB (500)
ECULIZUMAB (466)
VENETOCLAX (248)
DARBEPOETIN ALFA (213)
ADALIMUMAB (207)
LENALIDOMIDE (172)
RITUXIMAB (157)
ERYTHROPOIETIN (154)
IBRUTINIB (148)
DEXAMETHASONE (147)
Which SACITUZUMAB GOVITECAN Alternatives Have Lower Haemoglobin abnormal Risk?
SACITUZUMAB GOVITECAN vs SACITUZUMAB GOVITECAN-HZIY
SACITUZUMAB GOVITECAN vs SACROSIDASE
SACITUZUMAB GOVITECAN vs SACUBITRIL
SACITUZUMAB GOVITECAN vs SACUBITRIL\VALSARTAN
SACITUZUMAB GOVITECAN vs SAFINAMIDE