743 reports of this reaction
5.3% of all TENOFOVIR DISOPROXIL FUMARATE TABLETS reports
#2 most reported adverse reaction
VIROLOGIC FAILURE is the #2 most commonly reported adverse reaction for TENOFOVIR DISOPROXIL FUMARATE TABLETS, manufactured by Chartwell RX, LLC.. There are 743 FDA adverse event reports linking TENOFOVIR DISOPROXIL FUMARATE TABLETS to VIROLOGIC FAILURE. This represents approximately 5.3% of all 14,129 adverse event reports for this drug.
Patients taking TENOFOVIR DISOPROXIL FUMARATE TABLETS who experience virologic failure should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
VIROLOGIC FAILURE is moderately reported among TENOFOVIR DISOPROXIL FUMARATE TABLETS users, representing a notable but not dominant share of adverse events.
In addition to virologic failure, the following adverse reactions have been reported for TENOFOVIR DISOPROXIL FUMARATE TABLETS:
The following drugs have also been linked to virologic failure in FDA adverse event reports:
VIROLOGIC FAILURE has been reported as an adverse event in 743 FDA reports for TENOFOVIR DISOPROXIL FUMARATE TABLETS. This does not prove causation, but indicates an association observed in post-market surveillance data.
VIROLOGIC FAILURE accounts for approximately 5.3% of all adverse event reports for TENOFOVIR DISOPROXIL FUMARATE TABLETS, making it one of the most commonly reported side effect.
If you experience virologic failure while taking TENOFOVIR DISOPROXIL FUMARATE TABLETS, 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.