2,843 reports of this reaction
6.1% of all EMTRICITABINE AND TENOFOVIR ALAFENAMIDE reports
#2 most reported adverse reaction
CHRONIC KIDNEY DISEASE is the #2 most commonly reported adverse reaction for EMTRICITABINE AND TENOFOVIR ALAFENAMIDE, manufactured by Gilead Sciences, Inc.. There are 2,843 FDA adverse event reports linking EMTRICITABINE AND TENOFOVIR ALAFENAMIDE to CHRONIC KIDNEY DISEASE. This represents approximately 6.1% of all 46,639 adverse event reports for this drug.
Patients taking EMTRICITABINE AND TENOFOVIR ALAFENAMIDE 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 EMTRICITABINE AND TENOFOVIR ALAFENAMIDE 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 EMTRICITABINE AND TENOFOVIR ALAFENAMIDE:
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 2,843 FDA reports for EMTRICITABINE AND TENOFOVIR ALAFENAMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
CHRONIC KIDNEY DISEASE accounts for approximately 6.1% of all adverse event reports for EMTRICITABINE AND TENOFOVIR ALAFENAMIDE, making it one of the most commonly reported side effect.
If you experience chronic kidney disease while taking EMTRICITABINE AND TENOFOVIR ALAFENAMIDE, 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.