320 reports of this reaction
1.9% of all ASFOTASE ALFA reports
#11 most reported adverse reaction
INJECTION SITE PRURITUS is the #11 most commonly reported adverse reaction for ASFOTASE ALFA, manufactured by Alexion Pharmaceuticals, Inc.. There are 320 FDA adverse event reports linking ASFOTASE ALFA to INJECTION SITE PRURITUS. This represents approximately 1.9% of all 17,151 adverse event reports for this drug.
Patients taking ASFOTASE ALFA who experience injection site pruritus should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
INJECTION SITE PRURITUS is a less commonly reported adverse event for ASFOTASE ALFA, but still significant enough to appear in the safety profile.
In addition to injection site pruritus, the following adverse reactions have been reported for ASFOTASE ALFA:
The following drugs have also been linked to injection site pruritus in FDA adverse event reports:
INJECTION SITE PRURITUS has been reported as an adverse event in 320 FDA reports for ASFOTASE ALFA. This does not prove causation, but indicates an association observed in post-market surveillance data.
INJECTION SITE PRURITUS accounts for approximately 1.9% of all adverse event reports for ASFOTASE ALFA, making it a notable side effect.
If you experience injection site pruritus while taking ASFOTASE ALFA, 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.