3,842 reports of this reaction
4.3% of all METHADONE reports
#4 most reported adverse reaction
OVERDOSE is the #4 most commonly reported adverse reaction for METHADONE, manufactured by VistaPharm, LLC. There are 3,842 FDA adverse event reports linking METHADONE to OVERDOSE. This represents approximately 4.3% of all 88,944 adverse event reports for this drug.
Patients taking METHADONE who experience overdose should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OVERDOSE is moderately reported among METHADONE users, representing a notable but not dominant share of adverse events.
In addition to overdose, the following adverse reactions have been reported for METHADONE:
The following drugs have also been linked to overdose in FDA adverse event reports:
OVERDOSE has been reported as an adverse event in 3,842 FDA reports for METHADONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OVERDOSE accounts for approximately 4.3% of all adverse event reports for METHADONE, making it a notable side effect.
If you experience overdose 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.