Does GOLIMUMAB Cause Intercepted product preparation error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intercepted product preparation error have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.0% of all adverse event reports for GOLIMUMAB.
7
Reports of Intercepted product preparation error with GOLIMUMAB
0.0%
of all GOLIMUMAB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intercepted product preparation error From GOLIMUMAB?
Of the 7 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 GOLIMUMAB. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does GOLIMUMAB Cause?
Drug ineffective (17,959)
Rheumatoid arthritis (12,272)
Pain (11,443)
Fatigue (9,626)
Off label use (8,764)
Alopecia (8,394)
Rash (8,331)
Joint swelling (8,264)
Arthralgia (7,968)
Abdominal discomfort (7,902)
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 GOLIMUMAB Alternatives Have Lower Intercepted product preparation error Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN