1,057 reports of this reaction
1.2% of all HYDROCODONE BITARTRATE reports
#10 most reported adverse reaction
NAUSEA is the #10 most commonly reported adverse reaction for HYDROCODONE BITARTRATE, manufactured by Purdue Pharma LP. There are 1,057 FDA adverse event reports linking HYDROCODONE BITARTRATE to NAUSEA. This represents approximately 1.2% of all 89,079 adverse event reports for this drug.
Patients taking HYDROCODONE BITARTRATE who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is a less commonly reported adverse event for HYDROCODONE BITARTRATE, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for HYDROCODONE BITARTRATE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 1,057 FDA reports for HYDROCODONE BITARTRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 1.2% of all adverse event reports for HYDROCODONE BITARTRATE, making it a notable side effect.
If you experience nausea while taking HYDROCODONE BITARTRATE, 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.