Does GOLIMUMAB Cause Application site haemorrhage? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Application site haemorrhage have been filed in association with GOLIMUMAB (SIMPONI ARIA). This represents 0.0% of all adverse event reports for GOLIMUMAB.
26
Reports of Application site haemorrhage with GOLIMUMAB
0.0%
of all GOLIMUMAB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Application site haemorrhage From GOLIMUMAB?
Of the 26 reports, 1 (3.8%) required hospitalization.
Is Application site haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GOLIMUMAB. However, 26 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 Application site haemorrhage?
PEGFILGRASTIM (1,394)
MINOXIDIL (78)
BUPRENORPHINE (68)
ESTRADIOL (64)
DOCOSANOL (62)
BECAPLERMIN (60)
INGENOL MEBUTATE (50)
FENTANYL (47)
EVOLOCUMAB (45)
NICOTINE (37)
Which GOLIMUMAB Alternatives Have Lower Application site haemorrhage Risk?
GOLIMUMAB vs GOLODIRSEN
GOLIMUMAB vs GONADORELIN
GOLIMUMAB vs GONADOTROPHIN, CHORIONIC
GOLIMUMAB vs GOSERELIN
GOLIMUMAB vs GRAMICIDIN