ASTHENIA is the #10 most commonly reported adverse reaction for LEUPROLIDE ACETATE, manufactured by TOLMAR Inc.. There are 2,351 FDA adverse event reports linking LEUPROLIDE ACETATE to ASTHENIA. This represents approximately 1.8% of all 133,873 adverse event reports for this drug.
Patients taking LEUPROLIDE ACETATE who experience asthenia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
Reporting Frequency
ASTHENIA2,351 of 133,873 reports
ASTHENIA is a less commonly reported adverse event for LEUPROLIDE ACETATE, but still significant enough to appear in the safety profile.
Other Side Effects of LEUPROLIDE ACETATE
In addition to asthenia, the following adverse reactions have been reported for LEUPROLIDE ACETATE:
ASTHENIA has been reported as an adverse event in 2,351 FDA reports for LEUPROLIDE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is ASTHENIA with LEUPROLIDE ACETATE?
ASTHENIA accounts for approximately 1.8% of all adverse event reports for LEUPROLIDE ACETATE, making it a notable side effect.
What should I do if I experience ASTHENIA while taking LEUPROLIDE ACETATE?
If you experience asthenia 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.