37 reports of this reaction
3.1% of all TRIBASIC CALCIUM PHOSPHATE reports
#1 most reported adverse reaction
DIARRHOEA is the #1 most commonly reported adverse reaction for TRIBASIC CALCIUM PHOSPHATE, manufactured by DNA Labs, Inc.. There are 37 FDA adverse event reports linking TRIBASIC CALCIUM PHOSPHATE to DIARRHOEA. This represents approximately 3.1% of all 1,206 adverse event reports for this drug.
Patients taking TRIBASIC CALCIUM 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 TRIBASIC CALCIUM PHOSPHATE users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for TRIBASIC CALCIUM PHOSPHATE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 37 FDA reports for TRIBASIC CALCIUM PHOSPHATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 3.1% of all adverse event reports for TRIBASIC CALCIUM PHOSPHATE, making it one of the most commonly reported side effect.
If you experience diarrhoea while taking TRIBASIC CALCIUM 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.