Active substanceThiamineThiamine
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  • Dosage form: & nbspsolution for intramuscular injection
    Composition:
    Active substance: thiamine hydrochloride 50 mg
    Excipients: disodium edetate 0.1 mg, water for injection up to 1 ml.
    Description:Transparent colorless or almost colorless liquid with a weak characteristic odor.
    Pharmacotherapeutic group:Vitamin B1
    ATX: & nbsp

    A.11.D.A.01   Thiamine

    Pharmacodynamics:
    In the body it is converted into an active thiamine pyrophosphate and as a coenzyme is included in the pyruvate decarboxylase and alpha-ketoglutarate decarboxylase complexes,which participate in the oxidative decarboxylation of pyruvic and alpha-ketoglutaric acids; transketolase - an enzyme of the pentose phosphate shunt.
    Pharmacokinetics:
    In the blood, the concentration is relatively low, while in plasma there is a predominantly free thiamine, in erythrocytes and leukocytes its phosphoric, ethers. Phosphorylation occurs in the liver. The most active phosphoric ester is thiamine diphosphate, which possesses coenzyme activity. It accumulates mainly in the liver, heart, brain, kidneys, spleen. 1/2 of the total amount is contained in striated muscles and myocardium and about 40% in internal organs. It is excreted through the intestines and kidneys.
    Indications:
    Hypovitaminosis and vitamin B deficiency1, including in patients who are on probe nutrition, hemodialysis, with malabsorption syndrome.
    Contraindications:Increased individual sensitivity, pregnancy, lactation, children's age.
    Carefully:Encephalopathy Wernicke, premenopausal and climacteric period in women.
    Dosing and Administration:
    Intramuscularly (deep into the muscle).
    Begin the administration of the drug is recommended with small doses (not more than 0.5 ml of solution)
    and only with good tolerability, higher doses are administered.
    Adults appoint 20-50 mg of thiamine (0.5-1 ml) once a day.
    The course of treatment is 10-30 injections.
    Side effects:
    Allergic reactions (urticaria, skin itching, angioedema, rarely - anaphylactic shock), increased sweating, tachycardia. Soreness (due to low pH of solutions) with intramuscular injection is rare.
    Overdose:
    In case of an overdose of vitamin B1 increases the activity of acetylcholine, which plays an important role in the pathogenesis of allergies. Prolonged administration of excessive doses of vitamin B1 can lead to discoordination of the enzyme systems of the liver and its fatty degeneration, impaired renal function.
    Treatment: conduct symptomatic therapy.
    Interaction:
    Thiamine solution should not be mixed with solutions containing sulfites, t. in them it completely disintegrates. It is not recommended simultaneous parenteral administration of thiamine with pyridoxine or cyanocobalamin: pyridoxine makes it difficult to convert thiamine into a biologically active form, cyanocobalamin enhances the allergenic effect of thiamine. Do not mix in one syringe thiamine with benzylpenicillin or streptomycin (destruction of antibiotics), thiamine and nicotinic acid (destruction of thiamine). Thiamine reduces the pharmacological activity of suxamethonium iodide, phentolamine, propanolol, sympatholytics (reserpine), hypnotics (reduces hypnotics and hypotensive effects). Thiamine is unstable in alkaline and neutral solutions; administration with carbonates, citrates, barbiturates with Cu2+ not recommended.
    Special instructions:
    When determining the concentration of theophylline in the blood serum by the spectrophotometric method, urobilinogen can be distorted by Ehrlich's reagent (when taking high doses). Do not use instead of substitute - balanced diet, only in combination with diet therapy.
    Parenteral administration is recommended only if oral administration (nausea, vomiting, malabsorption syndrome, preoperative and / or postoperative conditions) is not possible. With Wernicke's encephalopathy, the administration of dextrose should precede the use of thiamine.
    Effect on the ability to drive transp. cf. and fur:

    Form release / dosage:
    Solution for intramuscular injection 50 mg / ml.
    Packaging:1 ml of the drug in neutral glass ampoules, with a notch marked with a dot (paint). 10 ampoules are placed in a contour mesh package made of a polyvinyl chloride film. 1 circuit cell pack together with instructions for use "is placed in a pack of cardboard.
    Storage conditions:
    In the dark place at a temperature of no higher than 25 ° C. Keep out of the reach of children.
    Shelf life:
    3 years.
    Do not use after expiry date.
    Terms of leave from pharmacies:On prescription
    Registration number:LP-001230
    Date of registration:17.11.2011
    Expiration Date:17.11.2016
    The owner of the registration certificate: Mapichem AG Mapichem AG Switzerland
    Manufacturer: & nbsp
    Representation: & nbspMapichem AGMapichem AG
    Information update date: & nbsp21.02.2017
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