703 reports of this reaction
5.0% of all TENOFOVIR DISOPROXIL FUMARATE TABLETS reports
#4 most reported adverse reaction
FOETAL EXPOSURE DURING PREGNANCY is the #4 most commonly reported adverse reaction for TENOFOVIR DISOPROXIL FUMARATE TABLETS, manufactured by Chartwell RX, LLC.. There are 703 FDA adverse event reports linking TENOFOVIR DISOPROXIL FUMARATE TABLETS to FOETAL EXPOSURE DURING PREGNANCY. This represents approximately 5.0% of all 14,129 adverse event reports for this drug.
Patients taking TENOFOVIR DISOPROXIL FUMARATE TABLETS who experience foetal exposure during pregnancy should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FOETAL EXPOSURE DURING PREGNANCY is moderately reported among TENOFOVIR DISOPROXIL FUMARATE TABLETS users, representing a notable but not dominant share of adverse events.
In addition to foetal exposure during pregnancy, the following adverse reactions have been reported for TENOFOVIR DISOPROXIL FUMARATE TABLETS:
The following drugs have also been linked to foetal exposure during pregnancy in FDA adverse event reports:
FOETAL EXPOSURE DURING PREGNANCY has been reported as an adverse event in 703 FDA reports for TENOFOVIR DISOPROXIL FUMARATE TABLETS. This does not prove causation, but indicates an association observed in post-market surveillance data.
FOETAL EXPOSURE DURING PREGNANCY accounts for approximately 5.0% of all adverse event reports for TENOFOVIR DISOPROXIL FUMARATE TABLETS, making it a notable side effect.
If you experience foetal exposure during pregnancy 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.