Does BELANTAMAB MAFODOTIN Cause Intentional product use issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intentional product use issue have been filed in association with BELANTAMAB MAFODOTIN (Blenrep). This represents 0.3% of all adverse event reports for BELANTAMAB MAFODOTIN.
7
Reports of Intentional product use issue with BELANTAMAB MAFODOTIN
0.3%
of all BELANTAMAB MAFODOTIN reports
1
Deaths
0
Hospitalizations
How Dangerous Is Intentional product use issue From BELANTAMAB MAFODOTIN?
Of the 7 reports, 1 (14.3%) resulted in death.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BELANTAMAB MAFODOTIN. However, 7 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which BELANTAMAB MAFODOTIN Alternatives Have Lower Intentional product use issue Risk?
BELANTAMAB MAFODOTIN vs BELANTAMAB MAFODOTIN-BLMF
BELANTAMAB MAFODOTIN vs BELATACEPT
BELANTAMAB MAFODOTIN vs BELIMUMAB
BELANTAMAB MAFODOTIN vs BELINOSTAT
BELANTAMAB MAFODOTIN vs BELUMOSUDIL