36,927 reports of this reaction
6.2% of all OXYCODONE HYDROCHLORIDE reports
#5 most reported adverse reaction
DRUG WITHDRAWAL SYNDROME is the #5 most commonly reported adverse reaction for OXYCODONE HYDROCHLORIDE, manufactured by Purdue Pharma LP. There are 36,927 FDA adverse event reports linking OXYCODONE HYDROCHLORIDE to DRUG WITHDRAWAL SYNDROME. This represents approximately 6.2% of all 594,683 adverse event reports for this drug.
OXYCODONE HYDROCHLORIDE has an overall safety score of 95 out of 100. Patients taking OXYCODONE HYDROCHLORIDE 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 moderately reported among OXYCODONE HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to drug withdrawal syndrome, the following adverse reactions have been reported for OXYCODONE HYDROCHLORIDE:
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 36,927 FDA reports for OXYCODONE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRUG WITHDRAWAL SYNDROME accounts for approximately 6.2% of all adverse event reports for OXYCODONE HYDROCHLORIDE, making it a notable side effect.
If you experience drug withdrawal syndrome while taking OXYCODONE HYDROCHLORIDE, 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.