Does BELATACEPT Cause Product storage error? 142 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 142 reports of Product storage error have been filed in association with BELATACEPT (NULOJIX). This represents 4.2% of all adverse event reports for BELATACEPT.
142
Reports of Product storage error with BELATACEPT
4.2%
of all BELATACEPT reports
1
Deaths
4
Hospitalizations
How Dangerous Is Product storage error From BELATACEPT?
Of the 142 reports, 1 (0.7%) resulted in death, 4 (2.8%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BELATACEPT. However, 142 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)
Acute kidney injury (137)
Covid-19 (129)
Hospitalisation (123)
Kidney transplant rejection (97)
Intentional product use issue (83)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which BELATACEPT Alternatives Have Lower Product storage error Risk?
BELATACEPT vs BELIMUMAB
BELATACEPT vs BELINOSTAT
BELATACEPT vs BELUMOSUDIL
BELATACEPT vs BELVIQ
BELATACEPT vs BELZUTIFAN