4,104 reports of this reaction
5.1% of all OXYCODONE AND ACETAMINOPHEN reports
#2 most reported adverse reaction
OVERDOSE is the #2 most commonly reported adverse reaction for OXYCODONE AND ACETAMINOPHEN, manufactured by Par Health USA, LLC. There are 4,104 FDA adverse event reports linking OXYCODONE AND ACETAMINOPHEN to OVERDOSE. This represents approximately 5.1% of all 80,165 adverse event reports for this drug.
Patients taking OXYCODONE AND ACETAMINOPHEN 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 AND ACETAMINOPHEN users, representing a notable but not dominant share of adverse events.
In addition to overdose, the following adverse reactions have been reported for OXYCODONE AND ACETAMINOPHEN:
The following drugs have also been linked to overdose in FDA adverse event reports:
OVERDOSE has been reported as an adverse event in 4,104 FDA reports for OXYCODONE AND ACETAMINOPHEN. This does not prove causation, but indicates an association observed in post-market surveillance data.
OVERDOSE accounts for approximately 5.1% of all adverse event reports for OXYCODONE AND ACETAMINOPHEN, making it one of the most commonly reported side effect.
If you experience overdose 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.