Does BELATACEPT Cause Intentional product use issue? 83 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 83 reports of Intentional product use issue have been filed in association with BELATACEPT (NULOJIX). This represents 2.4% of all adverse event reports for BELATACEPT.
83
Reports of Intentional product use issue with BELATACEPT
2.4%
of all BELATACEPT reports
4
Deaths
20
Hospitalizations
How Dangerous Is Intentional product use issue From BELATACEPT?
Of the 83 reports, 4 (4.8%) resulted in death, 20 (24.1%) required hospitalization, and 2 (2.4%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BELATACEPT. However, 83 reports have been filed with the FAERS database.
What Other Side Effects Does BELATACEPT Cause?
Off label use (304)
Death (206)
Transplant rejection (178)
Cytomegalovirus infection (142)
Drug ineffective (142)
Product storage error (142)
Acute kidney injury (137)
Covid-19 (129)
Hospitalisation (123)
Kidney transplant rejection (97)
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 BELATACEPT Alternatives Have Lower Intentional product use issue Risk?
BELATACEPT vs BELIMUMAB
BELATACEPT vs BELINOSTAT
BELATACEPT vs BELUMOSUDIL
BELATACEPT vs BELVIQ
BELATACEPT vs BELZUTIFAN