2,372 reports of this reaction
2.5% of all ENOXAPARIN SODIUM reports
#1 most reported adverse reaction
DYSPNOEA is the #1 most commonly reported adverse reaction for ENOXAPARIN SODIUM, manufactured by Sanofi-Aventis U.S. LLC. There are 2,372 FDA adverse event reports linking ENOXAPARIN SODIUM to DYSPNOEA. This represents approximately 2.5% of all 96,320 adverse event reports for this drug.
Patients taking ENOXAPARIN SODIUM 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 a less commonly reported adverse event for ENOXAPARIN SODIUM, but still significant enough to appear in the safety profile.
In addition to dyspnoea, the following adverse reactions have been reported for ENOXAPARIN SODIUM:
The following drugs have also been linked to dyspnoea in FDA adverse event reports:
DYSPNOEA has been reported as an adverse event in 2,372 FDA reports for ENOXAPARIN SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSPNOEA accounts for approximately 2.5% of all adverse event reports for ENOXAPARIN SODIUM, making it one of the most commonly reported side effect.
If you experience dyspnoea while taking ENOXAPARIN 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.