22 reports of this reaction
1.4% of all ALLOPURINOL SODIUM reports
#14 most reported adverse reaction
WEIGHT DECREASED is the #14 most commonly reported adverse reaction for ALLOPURINOL SODIUM, manufactured by Hikma Pharmaceuticals USA Inc.. There are 22 FDA adverse event reports linking ALLOPURINOL SODIUM to WEIGHT DECREASED. This represents approximately 1.4% of all 1,553 adverse event reports for this drug.
Patients taking ALLOPURINOL SODIUM who experience weight decreased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
WEIGHT DECREASED is a less commonly reported adverse event for ALLOPURINOL SODIUM, but still significant enough to appear in the safety profile.
In addition to weight decreased, the following adverse reactions have been reported for ALLOPURINOL SODIUM:
The following drugs have also been linked to weight decreased in FDA adverse event reports:
WEIGHT DECREASED has been reported as an adverse event in 22 FDA reports for ALLOPURINOL SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
WEIGHT DECREASED accounts for approximately 1.4% of all adverse event reports for ALLOPURINOL SODIUM, making it a notable side effect.
If you experience weight decreased while taking ALLOPURINOL SODIUM, 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.