1 reports of this reaction
7.7% of all CHILDRENS ALLERGY RELIEF reports
#5 most reported adverse reaction
HAEMOGLOBIN DECREASED is the #5 most commonly reported adverse reaction for CHILDRENS ALLERGY RELIEF, manufactured by Allegiant Health. There are 1 FDA adverse event reports linking CHILDRENS ALLERGY RELIEF to HAEMOGLOBIN DECREASED. This represents approximately 7.7% of all 13 adverse event reports for this drug.
Patients taking CHILDRENS ALLERGY RELIEF who experience haemoglobin decreased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HAEMOGLOBIN DECREASED is moderately reported among CHILDRENS ALLERGY RELIEF users, representing a notable but not dominant share of adverse events.
In addition to haemoglobin decreased, the following adverse reactions have been reported for CHILDRENS ALLERGY RELIEF:
The following drugs have also been linked to haemoglobin decreased in FDA adverse event reports:
HAEMOGLOBIN DECREASED has been reported as an adverse event in 1 FDA reports for CHILDRENS ALLERGY RELIEF. This does not prove causation, but indicates an association observed in post-market surveillance data.
HAEMOGLOBIN DECREASED accounts for approximately 7.7% of all adverse event reports for CHILDRENS ALLERGY RELIEF, making it a notable side effect.
If you experience haemoglobin decreased while taking CHILDRENS ALLERGY RELIEF, 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.