2,281 reports of this reaction
1.2% of all TIRZEPATIDE reports
#20 most reported adverse reaction
INJECTION SITE PRURITUS is the #20 most commonly reported adverse reaction for TIRZEPATIDE, manufactured by Eli Lilly and Company. There are 2,281 FDA adverse event reports linking TIRZEPATIDE to INJECTION SITE PRURITUS. This represents approximately 1.2% of all 196,029 adverse event reports for this drug.
TIRZEPATIDE has an overall safety score of 78 out of 100. Patients taking TIRZEPATIDE 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 TIRZEPATIDE, but still significant enough to appear in the safety profile.
In addition to injection site pruritus, the following adverse reactions have been reported for TIRZEPATIDE:
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 2,281 FDA reports for TIRZEPATIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
INJECTION SITE PRURITUS accounts for approximately 1.2% of all adverse event reports for TIRZEPATIDE, making it a notable side effect.
If you experience injection site pruritus while taking TIRZEPATIDE, 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.