34 reports of this reaction
3.3% of all FERROSOFERRIC PHOSPHATE reports
#1 most reported adverse reaction
DIARRHOEA is the #1 most commonly reported adverse reaction for FERROSOFERRIC PHOSPHATE, manufactured by DNA Labs. There are 34 FDA adverse event reports linking FERROSOFERRIC PHOSPHATE to DIARRHOEA. This represents approximately 3.3% of all 1,043 adverse event reports for this drug.
Patients taking FERROSOFERRIC PHOSPHATE who experience diarrhoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIARRHOEA is moderately reported among FERROSOFERRIC PHOSPHATE users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for FERROSOFERRIC PHOSPHATE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 34 FDA reports for FERROSOFERRIC PHOSPHATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 3.3% of all adverse event reports for FERROSOFERRIC PHOSPHATE, making it one of the most commonly reported side effect.
If you experience diarrhoea while taking FERROSOFERRIC PHOSPHATE, 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.