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Racetril 30 GFS

Racetril 30 GFS, Racecadotril, All Medicine
Racetril 30 GFS
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Racetril30 GFS



Description

Racecadotril is a pure intestinal antisecretory active substance. It decreases the intestinal hypersecretion of water and electrolytes induced by cholera toxin or inflammation and does not have effects on basal secretory activity.

Following oral administration, Racecadotril is rapidly absorbed and then hydrolysed to thiorphan, which is an inhibitor of enkephalinase, a cell membrane peptidase located in various tissues, notably the epithelium of the small intestine. This enzyme contributes both to the hydrolysis of exogenous peptides and to the breakdown of endogenous peptides such as enkephalins. Racecadotril protects enkephalins from enzymatic degradation thereby prolonging their action at enkephalinergic synapses in the small intestine and reducing hypersecretion. Racecadotril exerts rapid antidiarrhoeal action, without modifying the duration of intestinal transit.

Indications

Racecadotril is indicated for the symptomatic treatment of acute diarrhea.

Dosage & Administration

Adults: One capsule initially, regardless of the time of day. Then one capsule three times daily preferably before the main meals.

Children (from 3 months of age): Racecadotril granules should be administered together with oral rehydration. The recommended dose is determined according to body weight: 1.5 mg/kg per administration, three times daily.


Infants less than 9kg: one 10 mg sachet 3 times daily.
Infants from 9 kg to 13 kg: two 10 mg sachets 3 times daily.
Children from 13 kg to 27 kg: one 30mg sachet 3 times daily.
Children of more than 27 kg: two 30mg sachets 3 times daily.

Side Effects

Headache, erythema multiforme, urticaria, angioedema may be seen.

Precautions

The administration of Racecadotril does not modify the usual rehydration regimens. The presence of bloody stools and fever may indicate the presence of invasive bacteria as a reason for diarrhea or the presence of other severe disease. Racecadotril has not been tested in antibiotic-associated diarrhea and should therefore not be administered under these conditions. Caution should be taken in patients with renal or liver impairment.

Use in Pregnancy & Lactation

Due to a lack of clinical data, Racecadotril should not be administered to pregnant or breastfeeding women.

Drug Interaction

No drug interactions found. Joint treatment with Racecadotril and Loperamide or Nifuroxazide does not modify the kinetics of Racecadotril.

Over Dose

No cases of overdose have been reported. In adults, single doses above 2 g which is equivalent to 20 times the therapeutic dose, have been administered, and no harmful effects have been described.

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