Does BRENTUXIMAB VEDOTIN Cause Haemoglobin abnormal? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Haemoglobin abnormal have been filed in association with BRENTUXIMAB VEDOTIN (ADCETRIS). This represents 0.3% of all adverse event reports for BRENTUXIMAB VEDOTIN.
25
Reports of Haemoglobin abnormal with BRENTUXIMAB VEDOTIN
0.3%
of all BRENTUXIMAB VEDOTIN reports
1
Deaths
1
Hospitalizations
How Dangerous Is Haemoglobin abnormal From BRENTUXIMAB VEDOTIN?
Of the 25 reports, 1 (4.0%) resulted in death, 1 (4.0%) required hospitalization.
Is Haemoglobin abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRENTUXIMAB VEDOTIN. However, 25 reports have been filed with the FAERS database.
What Other Side Effects Does BRENTUXIMAB VEDOTIN Cause?
Off label use (1,370)
Neuropathy peripheral (695)
Pyrexia (693)
Febrile neutropenia (684)
Death (602)
Neutropenia (561)
Hodgkin's disease (512)
Nausea (392)
Diarrhoea (385)
Anaemia (374)
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 BRENTUXIMAB VEDOTIN Alternatives Have Lower Haemoglobin abnormal Risk?
BRENTUXIMAB VEDOTIN vs BREO ELLIPTA
BRENTUXIMAB VEDOTIN vs BREXANOLONE
BRENTUXIMAB VEDOTIN vs BREXPIPRAZOLE
BRENTUXIMAB VEDOTIN vs BREXUCABTAGENE AUTOLEUCEL
BRENTUXIMAB VEDOTIN vs BRIGATINIB