10,452 reports of this reaction
1.9% of all OXYCODONE reports
#10 most reported adverse reaction
DRUG WITHDRAWAL SYNDROME is the #10 most commonly reported adverse reaction for OXYCODONE, manufactured by Amneal Pharmaceuticals LLC. There are 10,452 FDA adverse event reports linking OXYCODONE to DRUG WITHDRAWAL SYNDROME. This represents approximately 1.9% 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 drug withdrawal syndrome should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRUG WITHDRAWAL SYNDROME is a less commonly reported adverse event for OXYCODONE, but still significant enough to appear in the safety profile.
In addition to drug withdrawal syndrome, the following adverse reactions have been reported for OXYCODONE:
The following drugs have also been linked to drug withdrawal syndrome in FDA adverse event reports:
DRUG WITHDRAWAL SYNDROME has been reported as an adverse event in 10,452 FDA reports for OXYCODONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRUG WITHDRAWAL SYNDROME accounts for approximately 1.9% of all adverse event reports for OXYCODONE, making it a notable side effect.
If you experience drug withdrawal syndrome 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.