62 reports of this reaction
1.9% of all ACETAMINOPHEN AND CODEINE PHOSPHATE reports
#8 most reported adverse reaction
ABDOMINAL PAIN is the #8 most commonly reported adverse reaction for ACETAMINOPHEN AND CODEINE PHOSPHATE, manufactured by Aurolife Pharma, LLC. There are 62 FDA adverse event reports linking ACETAMINOPHEN AND CODEINE PHOSPHATE to ABDOMINAL PAIN. This represents approximately 1.9% of all 3,182 adverse event reports for this drug.
Patients taking ACETAMINOPHEN AND CODEINE PHOSPHATE who experience abdominal pain should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ABDOMINAL PAIN 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 abdominal pain, the following adverse reactions have been reported for ACETAMINOPHEN AND CODEINE PHOSPHATE:
The following drugs have also been linked to abdominal pain in FDA adverse event reports:
ABDOMINAL PAIN has been reported as an adverse event in 62 FDA reports for ACETAMINOPHEN AND CODEINE PHOSPHATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL PAIN accounts for approximately 1.9% of all adverse event reports for ACETAMINOPHEN AND CODEINE PHOSPHATE, making it a notable side effect.
If you experience abdominal pain 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.