Angin-Heel diabetes pills 50s

The instruction for medical use of ANGIN-HEEL SD medicine the Trade name of Angin-heel sd the International unlicensed name Is not present the Dosage form of the Tablet Structure One Tablet contains active agents: Apis mellifica D4 of 30.0 mg Arnica montana D4 of 30.0 mg Atropa bella-donna D4 of 60.0 mg Hepar sulfuris D6 of 60.0 mg Hydrargyrum bicyanatum D8 of 30.0 mg Phytolacca americana D4 of 30.0 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 Other combinations of drugs for elimination of symptoms of cold. The ATX R05X code the Pharmacological Pharmacokinetics to Investigate properties pharmacokinetic properties of homeopathic medicines is not possible. The pharmacodynamics Angin-Heel of SD – homeopathic medicine, has anti-inflammatory, antiseptic, disintoxication action which is based on activation of protective forces of an organism and normalization of the broken functions at the expense of substances of plant, mineral and animal origin which are a part of drug. Indications - tonsillitis the Route of administration and doses the Single dose: the adult 1 tablet sublingual (before full resorption). To accept 3 times a day in 15 - 20 minutes prior to food or in an hour after a meal. In case of acute onset of a disease to accept a single dose every 30 - 60 minutes, in general to 12 tablets a day. In chronic diseases to rassasyvat 1 tablet in a mouth 1-3 times a day. After recovery Angin-Heel by SD 2 times a day within 3 - 5 days for the purpose of prevention of complications is recommended to continue administration of drug. Side effects - the increased salivation (administration of drug to cancel and consult with the doctor) - allergic reactions of the Contraindication - hypersensitivity to plants of family of Astrov (thistle family) and other active or auxiliary components of drug Medicinal interactions of Interaction with other medicines are not established. Special instructions Can temporarily become aggravated the available disease symptoms. In this case it is necessary to lower a dose of drug and to increase intervals between its receptions or to temporarily cancel administration of drug. If symptoms did not stop, it is necessary to see behind consultation a doctor. In case of the unspecified diagnosis of tonsillitis or at constantly renewing tonsillitis, and also if the increased temperature keeps more than 3 days or temperature exceeds 39 °C, it is necessary to consult with the doctor. Drug contains lactose therefore patients with a lactose intolerance, deficiency of Lapp-lactases enzyme and malabsorption of glucose galactose should not use drug. Use in pediatrics Experience of use of this drug by children has no sufficient documentary confirmation. 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 from 9 °C to 29 °C. To store out of children's reach! Not to apply a period of storage of 5 years 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 Address of the organization in the territory of the Republic of Kazakhstan: the accepting claim (offer) on quality of medicines from consumers, 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