491 reports of this reaction
3.1% of all AGALSIDASE BETA reports
#2 most reported adverse reaction
PAIN is the #2 most commonly reported adverse reaction for AGALSIDASE BETA, manufactured by Genzyme Corporation. There are 491 FDA adverse event reports linking AGALSIDASE BETA to PAIN. This represents approximately 3.1% of all 15,654 adverse event reports for this drug.
Patients taking AGALSIDASE BETA 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 moderately reported among AGALSIDASE BETA users, representing a notable but not dominant share of adverse events.
In addition to pain, the following adverse reactions have been reported for AGALSIDASE BETA:
The following drugs have also been linked to pain in FDA adverse event reports:
PAIN has been reported as an adverse event in 491 FDA reports for AGALSIDASE BETA. This does not prove causation, but indicates an association observed in post-market surveillance data.
PAIN accounts for approximately 3.1% of all adverse event reports for AGALSIDASE BETA, making it one of the most commonly reported side effect.
If you experience pain while taking AGALSIDASE BETA, 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.