1,525 reports of this reaction
1.2% of all EXENATIDE reports
#20 most reported adverse reaction
DRUG EFFECT DECREASED is the #20 most commonly reported adverse reaction for EXENATIDE, manufactured by AstraZeneca Pharmaceuticals LP. There are 1,525 FDA adverse event reports linking EXENATIDE to DRUG EFFECT DECREASED. This represents approximately 1.2% of all 130,422 adverse event reports for this drug.
Patients taking EXENATIDE who experience drug effect decreased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRUG EFFECT DECREASED is a less commonly reported adverse event for EXENATIDE, but still significant enough to appear in the safety profile.
In addition to drug effect decreased, the following adverse reactions have been reported for EXENATIDE:
The following drugs have also been linked to drug effect decreased in FDA adverse event reports:
DRUG EFFECT DECREASED has been reported as an adverse event in 1,525 FDA reports for EXENATIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRUG EFFECT DECREASED accounts for approximately 1.2% of all adverse event reports for EXENATIDE, making it a notable side effect.
If you experience drug effect decreased while taking EXENATIDE, 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.