Citovir-3 powder d / prig.r-ra cranberry 20g, No. 1

Special Price $23.28 Regular Price $31.00
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SKU
BIDL3181155
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Expiration Date: 05/2027

Russian Pharmacy name:

Цитовир-3 порошок д/приг.р-ра клюквенный 20г, №1

Citovir-3 powder d / prig.r-ra cranberry 20g, No. 1; 'Prevention and complex therapy of influenza and ARVI in adults and children from 1 year old.

The drug is taken orally 30 minutes before meals.
The therapeutic and prophylactic regimens are identical.
Children aged 1 to 3 years - 2 ml of syrup 3 times / day.
Children aged 3 to 6 years - 4 ml 3 times / day.
Children aged 6 to 10 years - 8 ml 3 times / day.
Children over the age of 10 years - 12 ml 3 times / day.
The course of application is 4 days. If after 3 days of treatment there is no improvement or symptoms worsen, or new symptoms appear, you should consult your doctor.
If necessary, the prophylaxis course is repeated after 3-4 weeks.
Rules for the preparation of oral solution
Add 40 ml of water (boiled, cooled to room temperature) to the bottle with the powder, shake well. The content should completely dissolve. The volume of the solution after adding water is 50 ml.
The drug should be taken only according to the method of administration and in the doses indicated in the instructions. If necessary, you should consult your doctor before taking the drug.
The drug should be used only according to the indications specified in the instructions.

Active ingredient: sodium alpha-glutamyl-tryptophan 0.15 mg; ascorbic acid 12 mg; bendazole hydrochloride 1.25 mg;

Excipients: in the preparation without flavoring: fructose - 386.6 mg; in a preparation with flavoring: fructose - 386.2 mg, flavor identical to natural 'Orange' or 'Cranberry', or 'Strawberry' - 0.4 mg.

  • Hypersensitivity to the components of the drug;

  • diabetes;

  • pregnancy;

  • children's age up to 1 year.

    With caution: in case of arterial hypertension, the patient should consult a doctor before taking the drug.

pharmachologic effect

An immunomodulatory drug, is a means of etiotropic and immunostimulating therapy, has an indirect antiviral effect against influenza A and B viruses and other viruses that cause acute respiratory viral diseases. The drug reduces the severity of the main clinical symptoms of influenza and SARS, and also reduces the duration of the manifestation of the symptoms of the disease.
Bendazol induces the production of endogenous interferon in the body, has an immunomodulatory effect (normalizes the body's immune response). Enzymes, the production of which is induced by interferon in cells of various organs, inhibit viral replication.
Alpha-glutamyl-tryptophan (thymogen) is a synergist of the immunomodulatory action of bendazole, normalizing the T-cell link of immunity.
Ascorbic acid activates the humoral link of immunity, normalizes capillary permeability, thereby reducing inflammation, and exhibits antioxidant properties, neutralizing oxygen radicals accompanying the inflammatory process, increases the body's resistance to infection.

Pharmacokinetics

When taken orally, the drug is completely absorbed from the gastrointestinal tract. Bioavailability of bendazole is about 80%, alpha-glutamyl-tryptophan is no more than 15%, ascorbic acid is up to 70%. Ascorbic acid is absorbed from the gastrointestinal tract (mainly in the jejunum). Plasma protein binding - 25%. Tmax after oral administration - 4 hours. It easily penetrates into leukocytes, platelets, and then into all tissues, penetrates the placental barrier. Diseases of the gastrointestinal tract (peptic ulcer and duodenal ulcer, intestinal motility disorders, helminthic invasion, giardiasis), the use of fresh vegetable and fruit juices, alkaline drinks reduce the binding of ascorbic acid in the intestine. Ascorbic acid is metabolized mainly in the liver with the formation of deoxyascorbic, then oxaloacetic and diketogulonic acids. It is excreted by the kidneys, through the intestines, with sweat,breast milk unchanged and in the form of metabolites.
The biotransformation products of bendazole in the blood are two conjugates formed as a result of methylation and carboethoxylation of the imino group of the imidazole ring of bendazole: 1-methyl-2-benzylbenzimidazole and 1-carboethoxy-2-benzylbenzimidazole. Bendazole metabolites are excreted in the urine.
Alpha-glutamyl-tryptophan is broken down by peptidases into L-glutamic acid and L-tryptophan, which are used by the body in protein synthesis.

Application during pregnancy and lactation

The drug is contraindicated for use in pregnancy due to insufficient clinical data.
During breastfeeding, use is possible if the intended benefit to the mother outweighs the potential risk to the child. If you need to take the drug during breastfeeding, you should consult your doctor.

special instructions

With repeated courses, it is recommended to control the concentration of glucose in the blood.
Influence on the ability to drive vehicles and control mechanisms
The drug does not affect the ability to drive vehicles and other potentially hazardous activities that require increased concentration of attention and speed of psychomotor reactions

Side effect

From the side of the cardiovascular system: it is possible - a short-term decrease in blood pressure.
Allergic reactions: possibly urticaria (in such cases, the use of the drug is stopped and symptomatic treatment, antihistamines are prescribed).
If you experience the above or any other side effects, you should consult your doctor.
If these side effects worsen, you should inform your doctor.
Contraindications for use

Interaction with other drugs

No interactions of alpha-glutamyl-tryptophan with drugs have been identified.
Bendazol prevents an increase in OPSS caused by non-selective beta-blockers. Strengthens the hypotensive effect (lowering blood pressure) of antihypertensive and diuretic drugs. Phentolamine enhances the hypotensive effect of bendazole.
Ascorbic acid increases the concentration of benzylpenicillin and tetracyclines in the blood. Improves intestinal absorption of iron preparations. Reduces the effectiveness of heparin and indirect anticoagulants. Acetylsalicylic acid (ASA), oral contraceptives, fresh juices, and alkaline drinks reduce absorption and absorption. With simultaneous use with ASA, urinary excretion of ascorbic acid increases and ASA excretion decreases. ASA reduces the absorption of ascorbic acid by about 30%. Ascorbic acid increases the risk of crystalluria when using drugs containing ASA and short-acting sulfonamides, slows down the excretion of acids by the kidneys, increases the excretion of drugs with an alkaline reaction (including alkaloids), and reduces the concentration of oral contraceptives in the blood.With simultaneous use, it reduces the chronotropic effect of isoprenaline. Reduces the therapeutic effect of antipsychotics (neuroleptics) - phenothiazine derivatives, tubular reabsorption of amphetamine and tricyclic antidepressants. Barbiturates and primidone increase the excretion of ascorbic acid in the urine.
Possible simultaneous use with antiviral drugs and symptomatic therapy for influenza and acute respiratory viral infections.
If the patient is taking the above drugs or other drugs, he should consult a doctor.

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