19,081 reports of this reaction
3.5% of all OXYCODONE reports
#4 most reported adverse reaction
OVERDOSE is the #4 most commonly reported adverse reaction for OXYCODONE, manufactured by Amneal Pharmaceuticals LLC. There are 19,081 FDA adverse event reports linking OXYCODONE to OVERDOSE. This represents approximately 3.5% of all 541,080 adverse event reports for this drug.
OXYCODONE has an overall safety score of 92 out of 100. Patients taking OXYCODONE 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 OXYCODONE users, representing a notable but not dominant share of adverse events.
In addition to overdose, the following adverse reactions have been reported for OXYCODONE:
The following drugs have also been linked to overdose in FDA adverse event reports:
OVERDOSE has been reported as an adverse event in 19,081 FDA reports for OXYCODONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OVERDOSE accounts for approximately 3.5% of all adverse event reports for OXYCODONE, making it a notable side effect.
If you experience overdose while taking OXYCODONE, 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.