PYREXIA is the #11 most commonly reported adverse reaction for ACETAMINOPHEN, manufactured by Kenvue Brands LLC. There are 19,560 FDA adverse event reports linking ACETAMINOPHEN to PYREXIA. This represents approximately 1.8% of all 1,089,938 adverse event reports for this drug.
Patients taking ACETAMINOPHEN who experience pyrexia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
Reporting Frequency
PYREXIA19,560 of 1,089,938 reports
PYREXIA is a less commonly reported adverse event for ACETAMINOPHEN, but still significant enough to appear in the safety profile.
Other Side Effects of ACETAMINOPHEN
In addition to pyrexia, the following adverse reactions have been reported for ACETAMINOPHEN:
PYREXIA has been reported as an adverse event in 19,560 FDA reports for ACETAMINOPHEN. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is PYREXIA with ACETAMINOPHEN?
PYREXIA accounts for approximately 1.8% of all adverse event reports for ACETAMINOPHEN, making it a notable side effect.
What should I do if I experience PYREXIA while taking ACETAMINOPHEN?
If you experience pyrexia while taking ACETAMINOPHEN, 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.