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 Carsil (Silymarin)
 Carsil (Silymarin)Introduction
 Carsil (Silymarin) a result of natural product
 Carsil mechanism of action
 Carsil pharmacological studies
 Carsil pharmacokinetic studies
 Tolerance to Carsil, toxicological studies
 Clinical use of Carsil
 Carsil in chronic liver disease (CLD)
 Carsil indications
 Carsil adverse reactions, contraindications, Administration and posology, Storage
 Table of contents
Carsil package insert
 Silymarin substance
 Carsil 80 tabl x 35 mg
Carsil (Silymarin) is a product of plant origin with hepatoprotective and antioxidative action. The active component of Carsil is Silymarin derived from Silibum Marianum (Milk Thistle, Bulgarian White Thorn). Silymarin, as the plant active ingredient of Carsil, has a consolidating effect on the cell membrane, thus protecting the liver from harmful impacts and facilitating the recovery of the impaired liver cells.
 
 
 
 
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  carsil (silymarin) home / 







Tolerance to Carsil (Silymarin)   
 

TOLERANCE TO CARSIL
 
 Toxicological studies
 The acute, subacute and chronic toxicity was studied.
 The toxic effects of Carsil were studied on laboratory animals: mice, rats and dogs.
 
 ACUTE TOXICITY
 
 No lethality was observed after administration of single oral doses as high as 20,000 mg/kg to mice and rats.
 No behavioral change and lethality were observed after administration of oral doses as high as 1,000 mg/kg to dogs.
 
 SUBACUTE AND CHRONIC TOXICITY
 
 No evidence of toxic changes of the chemical laboratory and pathohistological investigations were found in rats, after oral treatment with doses of 50, 200 and 1,000 mg/kg for 3 months.
 No evidence of toxic damage was detected in a chronic (6-month) trial on rats and dogs in doses of 10, 50, 100 and 200 mg/kg.
 
 TERATOLOGICAL STUDIES
 
 No evidence of embryotoxic and tetratogenic effect was found in trials performed on rats, after oral treatment for the whole gestation period with doses of 1,000 and 2,000 mg/kg, as well as on rabbits treated orally with a dose of 100 mg/kg.
 
 MUTAGENICITY STUDIES
 
 No evidence of existence of a mutagenic effect was found in rats, after oral treatment with doses of 10, 50, 200 mg/kg.

 
 
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