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Cobenfy Disease Interactions

There are 7 disease interactions with Cobenfy (trospium / xanomeline).

Major

Trospium (applies to Cobenfy) gastrointestinal retention

Major Potential Hazard, Moderate plausibility. Applicable conditions: Gastrointestinal Obstruction, Ulcerative Colitis, Myasthenia Gravis

The use of trospium is contraindicated in patients with gastric retention. Trospium reduces the tonus of smooth muscle and may decrease gastrointestinal motility, hence it should be used with caution in patients with conditions such as ulcerative colitis, intestinal atony and myasthenia gravis. Caution should be exercised when using this drug in patients with gastrointestinal obstructive disorders as it increases the risk of gastric retention.

Major

Trospium (applies to Cobenfy) narrow angle glaucoma

Major Potential Hazard, Moderate plausibility. Applicable conditions: Glaucoma (Narrow Angle)

The use of trospium is contraindicated in patients with uncontrolled narrow-angle glaucoma. In those patients being treated for narrow-angle glaucoma, trospium should only be used if the potential benefits outweigh the risks and in that circumstance only with careful monitoring.

Major

Trospium (applies to Cobenfy) urinary retention

Major Potential Hazard, Moderate plausibility.

Use of trospium is contraindicated in patients with urinary retention. Administer trospium with caution in patients with clinically significant bladder outflow obstruction because of the risk of urinary retention.

Major

Xanomeline (applies to Cobenfy) hepatic impairment

Major Potential Hazard, Moderate plausibility. Applicable conditions: Liver Disease

Use of xanomeline, a component of xanomeline-trospium, is contraindicated in patients with moderate or severe hepatic impairment (Child-Pugh B or C). Use is not recommended in patients with mild hepatic impairment (Child-Pugh A). Xanomeline was not studied in patients with severe hepatic impairment. Assess liver enzymes prior to therapy, and as clinically indicated.

Moderate

Trospium (applies to Cobenfy) alcoholism

Moderate Potential Hazard, Moderate plausibility.

The use of alcohol may enhance the drowsiness caused by anticholinergic agents. It is recommended that alcohol should not be consumed within 2 hours of trospium administration. Caution should be exercised when using this agent in alcoholic patients.

Moderate

Trospium (applies to Cobenfy) hepatic impairment

Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Liver Disease

Caution is advised when administering trospium to patients with moderate to severe hepatic impairment. There is no information regarding the effect of severe hepatic impairment on exposure to trospium.

Moderate

Trospium (applies to Cobenfy) renal impairment

Moderate Potential Hazard, Moderate plausibility. Applicable conditions: Renal Dysfunction

Trospium is known to be substantially excreted by the kidney, and the risk of adverse reactions may be greater in patients with impaired renal function. A reduced dose is recommended in patients with severe renal impairment (CrCl less than 30 mL/minute). The pharmacokinetics of trospium have not been studied in patients with CrCl 30 to 80 mL/min.

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Cobenfy drug interactions

There are 386 drug interactions with Cobenfy (trospium / xanomeline).

Cobenfy alcohol/food interactions

There are 2 alcohol/food interactions with Cobenfy (trospium / xanomeline).


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.