43 reports of this reaction
1.4% of all ACTIVATED CHARCOAL reports
#19 most reported adverse reaction
LACTIC ACIDOSIS is the #19 most commonly reported adverse reaction for ACTIVATED CHARCOAL, manufactured by Padagis US LLC. There are 43 FDA adverse event reports linking ACTIVATED CHARCOAL to LACTIC ACIDOSIS. This represents approximately 1.4% of all 3,053 adverse event reports for this drug.
Patients taking ACTIVATED CHARCOAL who experience lactic acidosis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
LACTIC ACIDOSIS is a less commonly reported adverse event for ACTIVATED CHARCOAL, but still significant enough to appear in the safety profile.
In addition to lactic acidosis, the following adverse reactions have been reported for ACTIVATED CHARCOAL:
The following drugs have also been linked to lactic acidosis in FDA adverse event reports:
LACTIC ACIDOSIS has been reported as an adverse event in 43 FDA reports for ACTIVATED CHARCOAL. This does not prove causation, but indicates an association observed in post-market surveillance data.
LACTIC ACIDOSIS accounts for approximately 1.4% of all adverse event reports for ACTIVATED CHARCOAL, making it a notable side effect.
If you experience lactic acidosis 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.