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SARIDON (ITALY)
1 tablet contains: active ingredients: paracetamol 250 mg, propyphenazone 150 mg, caffeine 50 mg.
26у.е.
Symptomatic treatment of headaches, dental pain, menstrual pain, postoperative and rheumatic pain; feverish conditions in colds and flu.
Action: Saridon contains paracetamol and propyphenazone, which are analgesic and antipyretic, as well as small doses of caffeine, which enhances the analgesic effect of paracetamol.
Contraindications:
Saridon® should not be used in cases of:
• Allergy to pyrazolone or related compounds (hypersensitivity to drugs containing phenazone, propyphenazone, aminophenazone, metamizole);
• Allergy to drugs containing phenylbutazone;
• Established hypersensitivity to paracetamol, acetylsalicylic acid, confirmed allergy to caffeine;
• Congenital deficiency of glucose-6-phosphate dehydrogenase (hemolytic anemia);
• Acute hepatic porphyria.
Special caution (dose reduction and dividing the daily dose into more frequent intakes) is required in the following cases:
• Hepatitis;
• Renal function impairment;
• Gilbert's syndrome (ranging from benign secondary jaundice to glucuronyltransferase deficiency);
• Hematopoietic disorders.
Saridon® is not prescribed for children under 12 years of age.
Method of administration and doses:
Saridon® is taken orally. Tablets should be taken with a sufficient amount of liquid.
Adults:
1–2 tablets per dose. Do not take more than 3 times a day.
Children aged 12 to 18 years:
1 tablet per dose. Do not take more than 3 times a day.
The duration of treatment should not exceed one week. It is not recommended to exceed the recommended dose.
The package contains 20 tablets.
Action: Saridon contains paracetamol and propyphenazone, which are analgesic and antipyretic, as well as small doses of caffeine, which enhances the analgesic effect of paracetamol.
Contraindications:
Saridon® should not be used in cases of:
• Allergy to pyrazolone or related compounds (hypersensitivity to drugs containing phenazone, propyphenazone, aminophenazone, metamizole);
• Allergy to drugs containing phenylbutazone;
• Established hypersensitivity to paracetamol, acetylsalicylic acid, confirmed allergy to caffeine;
• Congenital deficiency of glucose-6-phosphate dehydrogenase (hemolytic anemia);
• Acute hepatic porphyria.
Special caution (dose reduction and dividing the daily dose into more frequent intakes) is required in the following cases:
• Hepatitis;
• Renal function impairment;
• Gilbert's syndrome (ranging from benign secondary jaundice to glucuronyltransferase deficiency);
• Hematopoietic disorders.
Saridon® is not prescribed for children under 12 years of age.
Method of administration and doses:
Saridon® is taken orally. Tablets should be taken with a sufficient amount of liquid.
Adults:
1–2 tablets per dose. Do not take more than 3 times a day.
Children aged 12 to 18 years:
1 tablet per dose. Do not take more than 3 times a day.
The duration of treatment should not exceed one week. It is not recommended to exceed the recommended dose.
The package contains 20 tablets.
