676 reports of this reaction
3.5% of all SEVELAMER CARBONATE reports
#5 most reported adverse reaction
CHRONIC KIDNEY DISEASE is the #5 most commonly reported adverse reaction for SEVELAMER CARBONATE, manufactured by Genzyme Corporation. There are 676 FDA adverse event reports linking SEVELAMER CARBONATE to CHRONIC KIDNEY DISEASE. This represents approximately 3.5% of all 19,097 adverse event reports for this drug.
Patients taking SEVELAMER CARBONATE who experience chronic kidney disease should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
CHRONIC KIDNEY DISEASE is moderately reported among SEVELAMER CARBONATE users, representing a notable but not dominant share of adverse events.
In addition to chronic kidney disease, the following adverse reactions have been reported for SEVELAMER CARBONATE:
The following drugs have also been linked to chronic kidney disease in FDA adverse event reports:
CHRONIC KIDNEY DISEASE has been reported as an adverse event in 676 FDA reports for SEVELAMER CARBONATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
CHRONIC KIDNEY DISEASE accounts for approximately 3.5% of all adverse event reports for SEVELAMER CARBONATE, making it a notable side effect.
If you experience chronic kidney disease while taking SEVELAMER CARBONATE, 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.