8,327 reports of this reaction
6.7% of all TENOFOVIR DISOPROXIL FUMARATE reports
#3 most reported adverse reaction
SKELETAL INJURY is the #3 most commonly reported adverse reaction for TENOFOVIR DISOPROXIL FUMARATE, manufactured by Gilead Sciences, Inc.. There are 8,327 FDA adverse event reports linking TENOFOVIR DISOPROXIL FUMARATE to SKELETAL INJURY. This represents approximately 6.7% of all 123,510 adverse event reports for this drug.
TENOFOVIR DISOPROXIL FUMARATE has an overall safety score of 92 out of 100. Patients taking TENOFOVIR DISOPROXIL FUMARATE who experience skeletal injury should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SKELETAL INJURY is moderately reported among TENOFOVIR DISOPROXIL FUMARATE users, representing a notable but not dominant share of adverse events.
In addition to skeletal injury, the following adverse reactions have been reported for TENOFOVIR DISOPROXIL FUMARATE:
The following drugs have also been linked to skeletal injury in FDA adverse event reports:
SKELETAL INJURY has been reported as an adverse event in 8,327 FDA reports for TENOFOVIR DISOPROXIL FUMARATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
SKELETAL INJURY accounts for approximately 6.7% of all adverse event reports for TENOFOVIR DISOPROXIL FUMARATE, making it one of the most commonly reported side effect.
If you experience skeletal injury while taking 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.