16,432 reports of this reaction
9.8% of all EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE reports
#1 most reported adverse reaction
BONE DENSITY DECREASED is the #1 most commonly reported adverse reaction for EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE, manufactured by Gilead Sciences, Inc. There are 16,432 FDA adverse event reports linking EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE to BONE DENSITY DECREASED. This represents approximately 9.8% of all 167,978 adverse event reports for this drug.
Patients taking EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE who experience bone density decreased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BONE DENSITY DECREASED is moderately reported among EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE users, representing a notable but not dominant share of adverse events.
In addition to bone density decreased, the following adverse reactions have been reported for EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE:
The following drugs have also been linked to bone density decreased in FDA adverse event reports:
BONE DENSITY DECREASED has been reported as an adverse event in 16,432 FDA reports for EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
BONE DENSITY DECREASED accounts for approximately 9.8% of all adverse event reports for EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE, making it one of the most commonly reported side effect.
If you experience bone density decreased while taking EMTRICITABINE AND TENOFOVIR DISOPROXIL 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.