106 reports of this reaction
3.3% of all ACETAMINOPHEN AND CODEINE PHOSPHATE reports
#1 most reported adverse reaction
DYSPNOEA is the #1 most commonly reported adverse reaction for ACETAMINOPHEN AND CODEINE PHOSPHATE, manufactured by Aurolife Pharma, LLC. There are 106 FDA adverse event reports linking ACETAMINOPHEN AND CODEINE PHOSPHATE to DYSPNOEA. This represents approximately 3.3% of all 3,182 adverse event reports for this drug.
Patients taking ACETAMINOPHEN AND CODEINE PHOSPHATE who experience dyspnoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSPNOEA is moderately reported among ACETAMINOPHEN AND CODEINE PHOSPHATE users, representing a notable but not dominant share of adverse events.
In addition to dyspnoea, the following adverse reactions have been reported for ACETAMINOPHEN AND CODEINE PHOSPHATE:
The following drugs have also been linked to dyspnoea in FDA adverse event reports:
DYSPNOEA has been reported as an adverse event in 106 FDA reports for ACETAMINOPHEN AND CODEINE PHOSPHATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSPNOEA accounts for approximately 3.3% of all adverse event reports for ACETAMINOPHEN AND CODEINE PHOSPHATE, making it one of the most commonly reported side effect.
If you experience dyspnoea 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.