15 reports of this reaction
0.5% of all ACTIVATED CHARCOAL reports
#68 most reported adverse reaction
BLOOD POTASSIUM DECREASED is the #68 most commonly reported adverse reaction for ACTIVATED CHARCOAL, manufactured by Padagis US LLC. There are 15 FDA adverse event reports linking ACTIVATED CHARCOAL to BLOOD POTASSIUM DECREASED. This represents approximately 0.5% of all 3,053 adverse event reports for this drug.
ACTIVATED CHARCOAL has an overall safety score of 85 out of 100. Patients taking ACTIVATED CHARCOAL who experience blood potassium 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.
BLOOD POTASSIUM DECREASED is a less commonly reported adverse event for ACTIVATED CHARCOAL, but still significant enough to appear in the safety profile.
In addition to blood potassium decreased, the following adverse reactions have been reported for ACTIVATED CHARCOAL:
The following drugs have also been linked to blood potassium decreased in FDA adverse event reports:
BLOOD POTASSIUM DECREASED has been reported as an adverse event in 15 FDA reports for ACTIVATED CHARCOAL. This does not prove causation, but indicates an association observed in post-market surveillance data.
BLOOD POTASSIUM DECREASED accounts for approximately 0.5% of all adverse event reports for ACTIVATED CHARCOAL, making it a notable side effect.
If you experience blood potassium decreased while taking ACTIVATED CHARCOAL, 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.