727 reports of this reaction
1.5% of all ENALAPRIL MALEATE reports
#17 most reported adverse reaction
RENAL FAILURE ACUTE is the #17 most commonly reported adverse reaction for ENALAPRIL MALEATE, manufactured by Bausch Health US LLC. There are 727 FDA adverse event reports linking ENALAPRIL MALEATE to RENAL FAILURE ACUTE. This represents approximately 1.5% of all 48,429 adverse event reports for this drug.
Patients taking ENALAPRIL MALEATE who experience renal failure acute 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 ACUTE is a less commonly reported adverse event for ENALAPRIL MALEATE, but still significant enough to appear in the safety profile.
In addition to renal failure acute, the following adverse reactions have been reported for ENALAPRIL MALEATE:
The following drugs have also been linked to renal failure acute in FDA adverse event reports:
RENAL FAILURE ACUTE has been reported as an adverse event in 727 FDA reports for ENALAPRIL MALEATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
RENAL FAILURE ACUTE accounts for approximately 1.5% of all adverse event reports for ENALAPRIL MALEATE, making it a notable side effect.
If you experience renal failure acute while taking ENALAPRIL MALEATE, 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.