243 reports of this reaction
1.2% of all OXYMORPHONE HYDROCHLORIDE reports
#11 most reported adverse reaction
BACK INJURY is the #11 most commonly reported adverse reaction for OXYMORPHONE HYDROCHLORIDE, manufactured by Amneal Pharmaceuticals LLC. There are 243 FDA adverse event reports linking OXYMORPHONE HYDROCHLORIDE to BACK INJURY. This represents approximately 1.2% of all 20,768 adverse event reports for this drug.
Patients taking OXYMORPHONE HYDROCHLORIDE who experience back injury should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BACK INJURY is a less commonly reported adverse event for OXYMORPHONE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to back injury, the following adverse reactions have been reported for OXYMORPHONE HYDROCHLORIDE:
BACK INJURY has been reported as an adverse event in 243 FDA reports for OXYMORPHONE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
BACK INJURY accounts for approximately 1.2% of all adverse event reports for OXYMORPHONE HYDROCHLORIDE, making it a notable side effect.
If you experience back injury while taking OXYMORPHONE 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.