922 reports of this reaction
4.8% of all COLESEVELAM HYDROCHLORIDE reports
#2 most reported adverse reaction
NO ADVERSE EVENT is the #2 most commonly reported adverse reaction for COLESEVELAM HYDROCHLORIDE, manufactured by Cosette Pharmaceuticals, Inc.. There are 922 FDA adverse event reports linking COLESEVELAM HYDROCHLORIDE to NO ADVERSE EVENT. This represents approximately 4.8% of all 19,165 adverse event reports for this drug.
Patients taking COLESEVELAM HYDROCHLORIDE who experience no adverse event should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NO ADVERSE EVENT is moderately reported among COLESEVELAM HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.
In addition to no adverse event, the following adverse reactions have been reported for COLESEVELAM HYDROCHLORIDE:
The following drugs have also been linked to no adverse event in FDA adverse event reports:
NO ADVERSE EVENT has been reported as an adverse event in 922 FDA reports for COLESEVELAM HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NO ADVERSE EVENT accounts for approximately 4.8% of all adverse event reports for COLESEVELAM HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience no adverse event while taking COLESEVELAM HYDROCHLORIDE, 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.