6,818 reports of this reaction
1.7% of all DESOXIMETASONE reports
#11 most reported adverse reaction
HAND DEFORMITY is the #11 most commonly reported adverse reaction for DESOXIMETASONE, manufactured by Sun Pharmaceutical Industries, Inc.. There are 6,818 FDA adverse event reports linking DESOXIMETASONE to HAND DEFORMITY. This represents approximately 1.7% of all 393,622 adverse event reports for this drug.
Patients taking DESOXIMETASONE 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 DESOXIMETASONE, but still significant enough to appear in the safety profile.
In addition to hand deformity, the following adverse reactions have been reported for DESOXIMETASONE:
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 6,818 FDA reports for DESOXIMETASONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HAND DEFORMITY accounts for approximately 1.7% of all adverse event reports for DESOXIMETASONE, making it a notable side effect.
If you experience hand deformity while taking DESOXIMETASONE, 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.