1 reports of this reaction
1.9% of all CHILDRENS ACETAMINOPHEN reports
#11 most reported adverse reaction
BLOOD METHAEMOGLOBIN PRESENT is the #11 most commonly reported adverse reaction for CHILDRENS ACETAMINOPHEN, manufactured by AARNA USA INC.. There are 1 FDA adverse event reports linking CHILDRENS ACETAMINOPHEN to BLOOD METHAEMOGLOBIN PRESENT. This represents approximately 1.9% of all 52 adverse event reports for this drug.
Patients taking CHILDRENS ACETAMINOPHEN who experience blood methaemoglobin present should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BLOOD METHAEMOGLOBIN PRESENT is a less commonly reported adverse event for CHILDRENS ACETAMINOPHEN, but still significant enough to appear in the safety profile.
In addition to blood methaemoglobin present, the following adverse reactions have been reported for CHILDRENS ACETAMINOPHEN:
BLOOD METHAEMOGLOBIN PRESENT has been reported as an adverse event in 1 FDA reports for CHILDRENS ACETAMINOPHEN. This does not prove causation, but indicates an association observed in post-market surveillance data.
BLOOD METHAEMOGLOBIN PRESENT accounts for approximately 1.9% of all adverse event reports for CHILDRENS ACETAMINOPHEN, making it a notable side effect.
If you experience blood methaemoglobin present while taking CHILDRENS 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.