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Tolcapone and Hepatic dysfunction

Result of checking the interaction of drug Tolcapone and disease Hepatic dysfunction for safety when used together.

Check result:
Tolcapone <> Hepatic dysfunction
Relevance: 23.07.2019 Reviewer: Shkutko P.M., M.D., in

When checking interaction based on authoritative sources Drugs.com, Rxlist.com, Webmd.com, Medscape.com there are contraindications or side effects that may cause harm or increase the negative effect from drug use in presence of concomitant diseases.

Consumer:

Transaminase (AST/ALT) levels >3 times (occasionally 8 times) the upper limits of normal have occurred in 1% to 3% of patients administered tolcapone, depending on the dosage. Approximately 1/3 of these patients also developed diarrhea. Tolcapone is extensively metabolized by the liver to inactive forms and < 0.5% is eliminated unchanged by the kidney. A 50% reduction in clearance and volume of distribution has occurred in patients with moderate liver cirrhosis, resulting in a 2 fold increase in concentration of unbound tolcapone. Therapy with tolcapone should be administered cautiously in patients with compromised hepatic function. Clinical monitoring of hepatic function is recommended prior to initiation of tolcapone, monthly during the first 3 months, and every 6 weeks for the next 3 months of therapy.

References:
  • "Product Information. Tasmar (tolcapone)." Valeant Pharmaceuticals, Costa Mesa, CA.
Tolcapone

Generic Name: tolcapone

Brand Name: Tasmar

Synonyms: n.a.

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