1,204 reports of this reaction
4.1% of all METOLAZONE reports
#1 most reported adverse reaction
DYSPNOEA is the #1 most commonly reported adverse reaction for METOLAZONE, manufactured by Aarkish Pharmaceuticals NJ Inc.. There are 1,204 FDA adverse event reports linking METOLAZONE to DYSPNOEA. This represents approximately 4.1% of all 29,146 adverse event reports for this drug.
Patients taking METOLAZONE who experience dyspnoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSPNOEA is moderately reported among METOLAZONE users, representing a notable but not dominant share of adverse events.
In addition to dyspnoea, the following adverse reactions have been reported for METOLAZONE:
The following drugs have also been linked to dyspnoea in FDA adverse event reports:
DYSPNOEA has been reported as an adverse event in 1,204 FDA reports for METOLAZONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSPNOEA accounts for approximately 4.1% of all adverse event reports for METOLAZONE, making it one of the most commonly reported side effect.
If you experience dyspnoea 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.