Does BELATACEPT Cause Intercepted product preparation error? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Intercepted product preparation error have been filed in association with BELATACEPT (NULOJIX). This represents 0.4% of all adverse event reports for BELATACEPT.
12
Reports of Intercepted product preparation error with BELATACEPT
0.4%
of all BELATACEPT reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intercepted product preparation error From BELATACEPT?
Of the 12 reports.
Is Intercepted product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BELATACEPT. However, 12 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 Intercepted product preparation error?
LEUPROLIDE (8,621)
PEGFILGRASTIM (1,514)
DEVICE (1,033)
CARFILZOMIB (367)
BLINATUMOMAB (110)
BEVACIZUMAB-AWWB (54)
ROMIPLOSTIM (48)
TRASTUZUMAB-ANNS (42)
AFLIBERCEPT (39)
TOCILIZUMAB (26)
Which BELATACEPT Alternatives Have Lower Intercepted product preparation error Risk?
BELATACEPT vs BELIMUMAB
BELATACEPT vs BELINOSTAT
BELATACEPT vs BELUMOSUDIL
BELATACEPT vs BELVIQ
BELATACEPT vs BELZUTIFAN