695 reports of this reaction
3.0% of all CIMETIDINE reports
#3 most reported adverse reaction
RENAL FAILURE is the #3 most commonly reported adverse reaction for CIMETIDINE, manufactured by Medtech Products Inc.. There are 695 FDA adverse event reports linking CIMETIDINE to RENAL FAILURE. This represents approximately 3.0% of all 23,246 adverse event reports for this drug.
Patients taking CIMETIDINE who experience renal failure should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
RENAL FAILURE is a less commonly reported adverse event for CIMETIDINE, but still significant enough to appear in the safety profile.
In addition to renal failure, the following adverse reactions have been reported for CIMETIDINE:
The following drugs have also been linked to renal failure in FDA adverse event reports:
RENAL FAILURE has been reported as an adverse event in 695 FDA reports for CIMETIDINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
RENAL FAILURE accounts for approximately 3.0% of all adverse event reports for CIMETIDINE, making it one of the most commonly reported side effect.
If you experience renal failure while taking CIMETIDINE, 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.