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MEXIDOL® (Emoxipine) 125 mg, 50 coated tablets
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ARPEFLU (Umifenovir) 100 mg, 20/30 caps
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Description
The instruction for medical use of NEWREKSAN® medicine the Trade name of Nyureksan® the International unlicensed name Is not present the Dosage form of the Tablet Structure One Tablet contains active agents: Avena sativa D2 of 0.6 mg Coffea arabica D12 of 0.6 mg Passiflora incarnata D2 of 0.6 mg Zincum isovalerianicum D4 of 0.6 mg excipients: lactoses monohydrate, magnesium stearate. The description of the Tablet of round shape, with a flat surface, from white till ochroleucous color, with a facet. Flavourless. Pharmacotherapeutic group Drugs for treatment of diseases of nervous system. Drugs for treatment of diseases of nervous system others. The ATX N07X code the Pharmacological Pharmacokinetics to Investigate properties pharmacokinetic properties of homeopathic medicines is not possible. The pharmacodynamics of Nyureksan® represents complex homeopathic medicine. Ньюрексан® has the supporting action of nervous system, removes nervous concern and a sleep disorder. Effect of drug is based on own processes of regulation of an organism in elimination of nervousness, restoration of a dream and internal balance. Indications In complex therapy – at nervous concern and a sleep disorder the Route of administration and doses Inside. It is preferable to allow a tablet to be dissolved in a mouth, then to swallow. For children it is allowed to pound a tablet and to add to a small amount of water. Drug is used on an empty stomach or between meals. Standard dosage: Adults (and children from 12 years are also more senior): on 1 tablet 3 times a day. In pediatrics: To children from 6 do11 years: on 1 tablet 2 times a day. An initial dosage at acute condition: Adults (and children from 12 years are also more senior): on 1 tablet each 30 minutes – 1 hour, up to 12 tablets day then to continue in a standard dosage. In pediatrics: To children from 6 do11 years: on 1 tablet each 1-2 hours, up to 8 tablets a day then to continue in a standard dosage. The course of treatment individual is also appointed by the doctor. Side effects – reactions of hypersensitivity, such as skin allergic reactions – temporary deterioration in symptoms (initial aggravation) of the Contraindication – hypersensitivity to drug components – persons with hereditary intolerance of fructose, deficiency of Lapp-lactases enzyme, glucose galactose malabsorption Medicinal interactions Drug is compatible to other medicines. Special instructions If symptoms remain or worsen, it is necessary to consult immediately with the doctor. Drug contains lactose therefore patients with a lactose intolerance have to be informed on it. To Apply pregnancy and the period of a lactation only after preliminary consultation with the doctor. The feature of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms does not affect ability to run the vehicle or potentially dangerous mechanisms. Overdose Cases of overdose of drug are not described. The form of release and packing On 50 tablets place in a polypropylene container with a cover stopper from polypropylene. On 1 container together with the instruction for medical use in the state and Russian languages put in a pack from cardboard. To Store storage conditions in original packing at a temperature not above 30 °C. To store out of children’s reach! A period of storage of 5 years 12 months after the first opening of a container. Not to apply after the expiry date specified on packing! Prescription status Without prescription of Proizvoditel Biologishe Haylmittel Heel GmbH Dr. Rekeveg strasse 2-4, 76532 Baden-Baden, Germany the Owner of the registration certificate of Biologishe Haylmittel Heel GmbH Dr. Rekeveg strasse 2-4, 76532 Baden-Baden, Germany the Name, the address and a contact information of the organization in the territory of the Republic of Kazakhstan, the accepting claim (offer) on quality of medicines from consumers and responsible for post-registration observation of safety of medicine of AEM Services LLP 050040, RK, Almaty, Al-Farabi Ave., 75A, office 102-103 of aemservices@mail.ru +7 707 798 83 83
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