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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 BELANTAMAB MAFODOTIN Cause Sepsis? 38 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Sepsis have been filed in association with BELANTAMAB MAFODOTIN (Blenrep). This represents 1.7% of all adverse event reports for BELANTAMAB MAFODOTIN.

38
Reports of Sepsis with BELANTAMAB MAFODOTIN
1.7%
of all BELANTAMAB MAFODOTIN reports
21
Deaths
28
Hospitalizations

How Dangerous Is Sepsis From BELANTAMAB MAFODOTIN?

Of the 38 reports, 21 (55.3%) resulted in death, 28 (73.7%) required hospitalization, and 9 (23.7%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

Yes, Sepsis is listed as a known adverse reaction in the official FDA drug label for BELANTAMAB MAFODOTIN.

What Other Side Effects Does BELANTAMAB MAFODOTIN Cause?

Keratopathy (788) Visual acuity reduced (708) Death (499) Plasma cell myeloma (380) Dry eye (359) Night blindness (317) Photophobia (183) Foreign body sensation in eyes (151) Vision blurred (134) Ocular toxicity (94)

What Other Drugs Cause Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Which BELANTAMAB MAFODOTIN Alternatives Have Lower Sepsis Risk?

BELANTAMAB MAFODOTIN vs BELANTAMAB MAFODOTIN-BLMF BELANTAMAB MAFODOTIN vs BELATACEPT BELANTAMAB MAFODOTIN vs BELIMUMAB BELANTAMAB MAFODOTIN vs BELINOSTAT BELANTAMAB MAFODOTIN vs BELUMOSUDIL

Related Pages

BELANTAMAB MAFODOTIN Full Profile All Sepsis Reports All Drugs Causing Sepsis BELANTAMAB MAFODOTIN Demographics