1,659 reports of this reaction
1.9% of all METHADONE reports
#10 most reported adverse reaction
FOETAL EXPOSURE DURING PREGNANCY is the #10 most commonly reported adverse reaction for METHADONE, manufactured by VistaPharm, LLC. There are 1,659 FDA adverse event reports linking METHADONE to FOETAL EXPOSURE DURING PREGNANCY. This represents approximately 1.9% of all 88,944 adverse event reports for this drug.
Patients taking METHADONE 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 a less commonly reported adverse event for METHADONE, but still significant enough to appear in the safety profile.
In addition to foetal exposure during pregnancy, the following adverse reactions have been reported for METHADONE:
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 1,659 FDA reports for METHADONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FOETAL EXPOSURE DURING PREGNANCY accounts for approximately 1.9% of all adverse event reports for METHADONE, making it a notable side effect.
If you experience foetal exposure during pregnancy while taking METHADONE, 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.