7,867 reports of this reaction
5.9% of all LEUPROLIDE ACETATE reports
#4 most reported adverse reaction
SYRINGE ISSUE is the #4 most commonly reported adverse reaction for LEUPROLIDE ACETATE, manufactured by TOLMAR Inc.. There are 7,867 FDA adverse event reports linking LEUPROLIDE ACETATE to SYRINGE ISSUE. This represents approximately 5.9% of all 133,873 adverse event reports for this drug.
Patients taking LEUPROLIDE ACETATE who experience syringe issue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SYRINGE ISSUE is moderately reported among LEUPROLIDE ACETATE users, representing a notable but not dominant share of adverse events.
In addition to syringe issue, the following adverse reactions have been reported for LEUPROLIDE ACETATE:
SYRINGE ISSUE has been reported as an adverse event in 7,867 FDA reports for LEUPROLIDE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
SYRINGE ISSUE accounts for approximately 5.9% of all adverse event reports for LEUPROLIDE ACETATE, making it a notable side effect.
If you experience syringe issue while taking LEUPROLIDE ACETATE, 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.