6,927 reports of this reaction
1.4% of all GOLIMUMAB reports
#20 most reported adverse reaction
HAND DEFORMITY is the #20 most commonly reported adverse reaction for GOLIMUMAB, manufactured by Janssen Biotech, Inc.. There are 6,927 FDA adverse event reports linking GOLIMUMAB to HAND DEFORMITY. This represents approximately 1.4% of all 511,555 adverse event reports for this drug.
Patients taking GOLIMUMAB who experience hand deformity should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HAND DEFORMITY is a less commonly reported adverse event for GOLIMUMAB, but still significant enough to appear in the safety profile.
In addition to hand deformity, the following adverse reactions have been reported for GOLIMUMAB:
The following drugs have also been linked to hand deformity in FDA adverse event reports:
HAND DEFORMITY has been reported as an adverse event in 6,927 FDA reports for GOLIMUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
HAND DEFORMITY accounts for approximately 1.4% of all adverse event reports for GOLIMUMAB, making it a notable side effect.
If you experience hand deformity while taking GOLIMUMAB, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.