1,946 reports of this reaction
2.0% of all SELEXIPAG reports
#11 most reported adverse reaction
MYALGIA is the #11 most commonly reported adverse reaction for SELEXIPAG, manufactured by Actelion Pharmaceuticals US, Inc.. There are 1,946 FDA adverse event reports linking SELEXIPAG to MYALGIA. This represents approximately 2.0% of all 96,284 adverse event reports for this drug.
Patients taking SELEXIPAG who experience myalgia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MYALGIA is a less commonly reported adverse event for SELEXIPAG, but still significant enough to appear in the safety profile.
In addition to myalgia, the following adverse reactions have been reported for SELEXIPAG:
The following drugs have also been linked to myalgia in FDA adverse event reports:
MYALGIA has been reported as an adverse event in 1,946 FDA reports for SELEXIPAG. This does not prove causation, but indicates an association observed in post-market surveillance data.
MYALGIA accounts for approximately 2.0% of all adverse event reports for SELEXIPAG, making it a notable side effect.
If you experience myalgia while taking SELEXIPAG, 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.