434 reports of this reaction
1.5% of all ABACAVIR SULFATE reports
#19 most reported adverse reaction
RENAL FAILURE is the #19 most commonly reported adverse reaction for ABACAVIR SULFATE, manufactured by ViiV Healthcare Company. There are 434 FDA adverse event reports linking ABACAVIR SULFATE to RENAL FAILURE. This represents approximately 1.5% of all 29,564 adverse event reports for this drug.
Patients taking ABACAVIR SULFATE 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 ABACAVIR SULFATE, but still significant enough to appear in the safety profile.
In addition to renal failure, the following adverse reactions have been reported for ABACAVIR SULFATE:
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 434 FDA reports for ABACAVIR SULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
RENAL FAILURE accounts for approximately 1.5% of all adverse event reports for ABACAVIR SULFATE, making it a notable side effect.
If you experience renal failure while taking ABACAVIR SULFATE, 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.