BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE and CHRONIC KIDNEY DISEASE

3,595 reports of this reaction

5.7% of all BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE reports

#2 most reported adverse reaction

Overview

CHRONIC KIDNEY DISEASE is the #2 most commonly reported adverse reaction for BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE, manufactured by Gilead Sciences, Inc.. There are 3,595 FDA adverse event reports linking BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE to CHRONIC KIDNEY DISEASE. This represents approximately 5.7% of all 62,897 adverse event reports for this drug.

Patients taking BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE 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.

Reporting Frequency

CHRONIC KIDNEY DISEASE3,595 of 62,897 reports

CHRONIC KIDNEY DISEASE is moderately reported among BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE users, representing a notable but not dominant share of adverse events.

Other Side Effects of BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE

In addition to chronic kidney disease, the following adverse reactions have been reported for BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE:

Other Drugs Associated with CHRONIC KIDNEY DISEASE

The following drugs have also been linked to chronic kidney disease in FDA adverse event reports:

ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDEALUMINUM HYDROXIDE AND MAGNESIUM CARBONATEAMMONIUM LACTATEAMOXICILLINAMPICILLINAMPICILLIN SODIUMASPIRIN AND CAFFEINEATAZANAVIRAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONEAZITHROMYCINAZITHROMYCIN DIHYDRATEAZITHROMYCIN MONOHYDRATEBARIUM SULFATEBENZOCAINE AND MENTHOLBENZONATATEBISMUTH SUBSALICYLATEBUFFERED ASPIRINBUMETANIDECALCITRIOLCALCITRIOL CAPSULES 0.25 MCG

Frequently Asked Questions

Does BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE cause CHRONIC KIDNEY DISEASE?

CHRONIC KIDNEY DISEASE has been reported as an adverse event in 3,595 FDA reports for BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is CHRONIC KIDNEY DISEASE with BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE?

CHRONIC KIDNEY DISEASE accounts for approximately 5.7% of all adverse event reports for BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE, making it one of the most commonly reported side effect.

What should I do if I experience CHRONIC KIDNEY DISEASE while taking BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE?

If you experience chronic kidney disease while taking BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE, 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.

Related Pages

BICTEGRAVIR SODIUM, EMTRICITABINE, AND TENOFOVIR ALAFENAMIDE FUMARATE Full ProfileAll Drugs Causing CHRONIC KIDNEY DISEASEGilead Sciences, Inc. Drugs
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.