48 reports of this reaction
1.5% of all ACETAMINOPHEN AND CODEINE PHOSPHATE reports
#13 most reported adverse reaction
OEDEMA PERIPHERAL is the #13 most commonly reported adverse reaction for ACETAMINOPHEN AND CODEINE PHOSPHATE, manufactured by Aurolife Pharma, LLC. There are 48 FDA adverse event reports linking ACETAMINOPHEN AND CODEINE PHOSPHATE to OEDEMA PERIPHERAL. This represents approximately 1.5% of all 3,182 adverse event reports for this drug.
Patients taking ACETAMINOPHEN AND CODEINE PHOSPHATE who experience oedema peripheral should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OEDEMA PERIPHERAL is a less commonly reported adverse event for ACETAMINOPHEN AND CODEINE PHOSPHATE, but still significant enough to appear in the safety profile.
In addition to oedema peripheral, the following adverse reactions have been reported for ACETAMINOPHEN AND CODEINE PHOSPHATE:
The following drugs have also been linked to oedema peripheral in FDA adverse event reports:
OEDEMA PERIPHERAL has been reported as an adverse event in 48 FDA reports for ACETAMINOPHEN AND CODEINE PHOSPHATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OEDEMA PERIPHERAL accounts for approximately 1.5% of all adverse event reports for ACETAMINOPHEN AND CODEINE PHOSPHATE, making it a notable side effect.
If you experience oedema peripheral while taking ACETAMINOPHEN AND CODEINE PHOSPHATE, 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.