3,102 reports of this reaction
3.9% of all OXYCODONE AND ACETAMINOPHEN reports
#3 most reported adverse reaction
ILL DEFINED DISORDER is the #3 most commonly reported adverse reaction for OXYCODONE AND ACETAMINOPHEN, manufactured by Par Health USA, LLC. There are 3,102 FDA adverse event reports linking OXYCODONE AND ACETAMINOPHEN to ILL DEFINED DISORDER. This represents approximately 3.9% of all 80,165 adverse event reports for this drug.
Patients taking OXYCODONE AND ACETAMINOPHEN who experience ill defined disorder should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ILL DEFINED DISORDER is moderately reported among OXYCODONE AND ACETAMINOPHEN users, representing a notable but not dominant share of adverse events.
In addition to ill defined disorder, the following adverse reactions have been reported for OXYCODONE AND ACETAMINOPHEN:
The following drugs have also been linked to ill defined disorder in FDA adverse event reports:
ILL DEFINED DISORDER has been reported as an adverse event in 3,102 FDA reports for OXYCODONE AND ACETAMINOPHEN. This does not prove causation, but indicates an association observed in post-market surveillance data.
ILL DEFINED DISORDER accounts for approximately 3.9% of all adverse event reports for OXYCODONE AND ACETAMINOPHEN, making it one of the most commonly reported side effect.
If you experience ill defined disorder while taking OXYCODONE AND ACETAMINOPHEN, 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.