11 reports of this reaction
1.9% of all ACETAMINOPHEN, IBUPROFEN reports
#10 most reported adverse reaction
OVERDOSE is the #10 most commonly reported adverse reaction for ACETAMINOPHEN, IBUPROFEN, manufactured by WALGREENS. There are 11 FDA adverse event reports linking ACETAMINOPHEN, IBUPROFEN to OVERDOSE. This represents approximately 1.9% of all 567 adverse event reports for this drug.
Patients taking ACETAMINOPHEN, IBUPROFEN who experience overdose should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OVERDOSE is a less commonly reported adverse event for ACETAMINOPHEN, IBUPROFEN, but still significant enough to appear in the safety profile.
In addition to overdose, the following adverse reactions have been reported for ACETAMINOPHEN, IBUPROFEN:
The following drugs have also been linked to overdose in FDA adverse event reports:
OVERDOSE has been reported as an adverse event in 11 FDA reports for ACETAMINOPHEN, IBUPROFEN. This does not prove causation, but indicates an association observed in post-market surveillance data.
OVERDOSE accounts for approximately 1.9% of all adverse event reports for ACETAMINOPHEN, IBUPROFEN, making it a notable side effect.
If you experience overdose while taking ACETAMINOPHEN, IBUPROFEN, 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.