952 reports of this reaction
2.2% of all Praluent reports
#7 most reported adverse reaction
PAIN is the #7 most commonly reported adverse reaction for Praluent, manufactured by Regeneron Pharmaceuticals, Inc.. There are 952 FDA adverse event reports linking Praluent to PAIN. This represents approximately 2.2% of all 42,517 adverse event reports for this drug.
Patients taking Praluent who experience pain should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PAIN is a less commonly reported adverse event for Praluent, but still significant enough to appear in the safety profile.
In addition to pain, the following adverse reactions have been reported for Praluent:
The following drugs have also been linked to pain in FDA adverse event reports:
PAIN has been reported as an adverse event in 952 FDA reports for Praluent. This does not prove causation, but indicates an association observed in post-market surveillance data.
PAIN accounts for approximately 2.2% of all adverse event reports for Praluent, making it a notable side effect.
If you experience pain while taking Praluent, 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.