Sodium chloride of 0,9%
Producer: Federal state unitary enterprise NPO Mikrogen Russia
Code of automatic telephone exchange: B05CB01, B05XA03
Release form: Liquid dosage forms. Solvent for preparation of solution for injections.
General characteristics. Structure:
Active ingredient: 9 mg of sodium of chloride.
Excipients: water for injections.
Indications to use:
Dissolution and cultivation of medicines.
Route of administration and doses:
Subcutaneously, intramusculary, intravenously after dissolution or cultivation of medicines. Preparation of solutions of medicines with solvent chloride sodium use for preparation of dosage forms for injections of 0,9% is carried out in sterile conditions (opening of ampoules, filling of the syringe and tanks with medicines).
The amount of sodium of chloride of solvent for preparation of dosage forms for injections of 0,9% for the purpose of preparation of solution of specific means is defined by the application instruction of the last or depending on a situation - the doctor.
Features of use:
Pregnancy and lactation. The possibility of use at pregnancy and during breastfeeding is defined by properties of medicine, for dissolution or cultivation of which solvent was used.
Influence on ability to manage vehicles and mechanisms. Influence on ability to manage vehicles, mechanisms is defined by properties of medicine, for dissolution or cultivation of which solvent was used.
Side effects:
Side effects are defined by side effects of medicine, for dissolution or cultivation of which solvent was used.
Interaction with other medicines:
When mixing with other medicines it is necessary to control visually compatibility (nevertheless invisible and therapeutic incompatibility is possible).
Contraindications:
Sodium chloride solvent for injections of 0,9% as solvent of medicines is not applied to preparation of dosage forms if as obligatory for some of them other solvent is specified.
Overdose:
It is not described.
Storage conditions:
To store at a temperature not above 25 °C. To store in the place, unavailable to children. A period of validity - 5 years. Not to use after the period of validity specified on packaging.
Issue conditions:
According to the recipe
Packaging:
Solution for injections of 0,9% in ampoules on 1 ml, 2 ml, 5 ml or 10 ml. On 10 ampoules with the application instruction, a knife ampoule or the scarificator ampoule in a pack or a box from a cardboard. On 5 ampoules in a blister strip packaging. On the 2nd blister strip packagings with the application instruction, a knife ampoule or the scarificator ampoule in a pack from a cardboard. When packaging the ampoules having a ring of a break or a point for opening the knife ampoule or the scarificator ampoule is not put. On 5 ampoules in cassette planimetric packaging. On 2 cassette planimetric packagings with the application instruction in a pack from a cardboard. The complete set with dry dosage forms of drugs in the corresponding quantities is possible. Packaging: solvent for preparation of dosage forms for injections, 0.9% (ampoule) of 1/2/5/10 ml x 10 (a pack/box cardboard) the complete set with dry dosage forms of drugs in the corresponding quantities Is possible