525 reports of this reaction
1.8% of all METOLAZONE reports
#14 most reported adverse reaction
OEDEMA PERIPHERAL is the #14 most commonly reported adverse reaction for METOLAZONE, manufactured by Aarkish Pharmaceuticals NJ Inc.. There are 525 FDA adverse event reports linking METOLAZONE to OEDEMA PERIPHERAL. This represents approximately 1.8% of all 29,146 adverse event reports for this drug.
Patients taking METOLAZONE who experience oedema peripheral should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OEDEMA PERIPHERAL is a less commonly reported adverse event for METOLAZONE, but still significant enough to appear in the safety profile.
In addition to oedema peripheral, the following adverse reactions have been reported for METOLAZONE:
The following drugs have also been linked to oedema peripheral in FDA adverse event reports:
OEDEMA PERIPHERAL has been reported as an adverse event in 525 FDA reports for METOLAZONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OEDEMA PERIPHERAL accounts for approximately 1.8% of all adverse event reports for METOLAZONE, making it a notable side effect.
If you experience oedema peripheral while taking METOLAZONE, 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.