278 reports of this reaction
1.8% of all RANOLAZINE reports
#11 most reported adverse reaction
MALAISE is the #11 most commonly reported adverse reaction for RANOLAZINE, manufactured by A2A Integrated Pharmaceuticals. There are 278 FDA adverse event reports linking RANOLAZINE to MALAISE. This represents approximately 1.8% of all 15,363 adverse event reports for this drug.
Patients taking RANOLAZINE who experience malaise should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MALAISE is a less commonly reported adverse event for RANOLAZINE, but still significant enough to appear in the safety profile.
In addition to malaise, the following adverse reactions have been reported for RANOLAZINE:
The following drugs have also been linked to malaise in FDA adverse event reports:
MALAISE has been reported as an adverse event in 278 FDA reports for RANOLAZINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
MALAISE accounts for approximately 1.8% of all adverse event reports for RANOLAZINE, making it a notable side effect.
If you experience malaise while taking RANOLAZINE, 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.