Does BELANTAMAB MAFODOTIN Cause Condition aggravated? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Condition aggravated have been filed in association with BELANTAMAB MAFODOTIN (Blenrep). This represents 2.5% of all adverse event reports for BELANTAMAB MAFODOTIN.
57
Reports of Condition aggravated with BELANTAMAB MAFODOTIN
2.5%
of all BELANTAMAB MAFODOTIN reports
13
Deaths
16
Hospitalizations
How Dangerous Is Condition aggravated From BELANTAMAB MAFODOTIN?
Of the 57 reports, 13 (22.8%) resulted in death, 16 (28.1%) required hospitalization, and 1 (1.8%) 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 BELANTAMAB MAFODOTIN. However, 57 reports have been filed with the FAERS database.
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 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 BELANTAMAB MAFODOTIN Alternatives Have Lower Condition aggravated Risk?
BELANTAMAB MAFODOTIN vs BELANTAMAB MAFODOTIN-BLMF
BELANTAMAB MAFODOTIN vs BELATACEPT
BELANTAMAB MAFODOTIN vs BELIMUMAB
BELANTAMAB MAFODOTIN vs BELINOSTAT
BELANTAMAB MAFODOTIN vs BELUMOSUDIL