CLARANTIN Hard capsule Ref.[50022] Active ingredients: Naftidrofuryl

Source: Υπουργείο Υγείας (CY)  Revision Year: 2014  Publisher: Medochemie Ltd, 1-10 Constantinopoleos Street, 3011 Limassol, Cyprus

5.1. Pharmacodynamic properties

Pharmacotherapeutic group: Other peripheral vasodilators, Cardiovascular system
ATC code: C04AX21

Naftidrofuryl oxalate is a powerful spasmolytic agent. It also has a direct effect on intracellular metabolism. It produces an increase of ATP levels and a decrease of lactic acid levels in ischaemic conditions evidence for an enhancement of cellular oxidative capacity.

5.2. Pharmacokinetic properties

Naftidrofuryl oxalate is well absorbed when given orally. Peak plasma levels occur about 30 minutes after dosing and the half-life is about an hour although inter subject variation is relatively high. Accumulation does not occur at a dose level of 200mg three times daily.

The drug becomes extensively bound to plasma proteins and is excreted principally via the urine, all in the form of metabolites.

5.3. Preclinical safety data

In animal studies no toxic effects were seen. In repeated dose studies the no effect level was 25 mg/kg/day or greater. There was no evidence of effects on reproduction below doses which caused maternal toxicity.

© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.