411 reports of this reaction
3.3% of all ACETAMINOPHEN, CAFFEINE reports
#3 most reported adverse reaction
NAUSEA is the #3 most commonly reported adverse reaction for ACETAMINOPHEN, CAFFEINE, manufactured by Haleon US Holdings LLC. There are 411 FDA adverse event reports linking ACETAMINOPHEN, CAFFEINE to NAUSEA. This represents approximately 3.3% of all 12,550 adverse event reports for this drug.
Patients taking ACETAMINOPHEN, CAFFEINE 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 moderately reported among ACETAMINOPHEN, CAFFEINE users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for ACETAMINOPHEN, CAFFEINE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 411 FDA reports for ACETAMINOPHEN, CAFFEINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.3% of all adverse event reports for ACETAMINOPHEN, CAFFEINE, making it one of the most commonly reported side effect.
If you experience nausea while taking ACETAMINOPHEN, CAFFEINE, 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.