Sodium chloride B. Brown - instructions for use, dose, side effects, contraindications

Active substance:
Sodium chloride	9.00 g
Excipient:
Water for injections	up to 1000 ml
Concentration of electrolytes:
Na⁺	154 mmol / l
Cl^-	154 mmol / l
Physico-chemical characteristics:
Theoretical osmolality	308 mOsm / l
pH	4,5-7,0

Description:

A clear, colorless solution.

Pharmacotherapeutic group:Solvent

ATX: & nbsp

B.05.C.B.01 Sodium chloride

B.05.X.A.03 Sodium chloride

Pharmacodynamics:

A solution of sodium chloride 0.9% is isotonic with human blood plasma.

Pharmacokinetics:

It is excreted by the kidneys.

Indications:

Dissolution and dilution of compatible drugs or electrolyte concentrates in the preparation of dosage forms for injection.

Contraindications:

Do not use if another solvent is listed in the instructions for use of the dissolving / diluting drug.

Carefully:

The drug should be used with caution in hypernatremia and hyperchloremia.

Pregnancy and lactation:

The use during pregnancy and during breastfeeding is determined by the instruction of the preparation for dissolution / dilution of which will be applied sodium chloride, a solvent for the preparation of dosage forms for injection.

Dosing and Administration:

Mode of application

Intravenously, intramuscularly, subcutaneously in accordance with the instruction for the use of dissolved / diluted drugs.

Before using the drug sodium chloride, a solvent for the preparation of dosage forms for injection for dissolution and dilution of drugs, it is necessary to read the instructions for the use of these drugs.During the preparation of dosage forms with the use of sodium chloride, a solvent for the preparation of dosage forms for injections, it is necessary to follow the rules of aseptic (opening the ampoule, filling the syringe or other containers with medications).

Doses

The amount of sodium chloride, a solvent for the preparation of dosage forms for injection, is selected based on the required concentration of the dissolved / diluted preparation or electrolyte concentrate.

Side effects:

When using the drug according to the instructions, adverse side effects are not expected.

Interaction:

Sodium chloride is compatible with colloidal hemodynamic blood substitutes.

When mixed with other drugs or concentrates of electrolytes, it is necessary to visually check compatibility. There may be an invisible and therapeutic incompatibility.

Special instructions:

The drug should be used immediately after opening the ampoule or after preparing ready-to-use dosage forms.

Ampoules are for single use only. Remaining unused quantities of the drug are subject to destruction.

Use the solution only if it is clear and the ampoule is not damaged.

From the standpoint of microbiological safety, ready-to-use dosage forms obtained by dilution / dilution with the drug sodium chloride, solvent for the preparation of dosage forms for injection in compliance with the rules of aseptic, should be used immediately. If these dosage forms are not used immediately, the storage period at a temperature of 2 to 8 ° C should not exceed 24 hours.

Effect on the ability to drive transp. cf. and fur:

The influence on the ability to drive vehicles and mechanisms is determined by the instruction of the preparation whose dissolution / dilution is applied sodium chloride, a solvent for the preparation of dosage forms for injection.

Form release / dosage:

Solvent for preparing dosage forms for injection, 0.9%.

Packaging:

5 ml, 10 ml or 20 ml into ampoules made of polyethylene. corresponding to the requirements of the European Pharmacopoeia for polyethylene for parenteral preparations. Ampoules are of two types. Type I - colorless polyethylene ampoules, having a rectangular self-falling body with a twisting cap with a screw connection for needleless sampling of the preparation. A type II - colorless polyethylene ampoules having a cylindrical body with a twisting cap without screw connection for needleless sampling of the preparation.

By 10 ml or 20 ml into ampoules of polypropylene that meets the requirements of the European Pharmacopoeia for polypropylene for parenteral preparations.

Ampoules are transparent, they have a rectangular body with a twisting cap with a screw connection for needleless sampling of the preparation.

For 20 ampoules of 5 ml, 10 ml or 20 ml together with instructions for use in a cardboard pack.

For 100 ampoules of 10 ml or 20 ml together with instructions for use in a cardboard pack.

Storage conditions:

Store at a temperature not exceeding 25 ° C.

Keep out of the reach of children.

Shelf life:

3 years.

Do not use after the expiry date printed on the package.

Terms of leave from pharmacies:On prescription

Registration number:LP-002225

Date of registration:11.09.2013 / 28.01.2015

Expiration Date:11.09.2018

The owner of the registration certificate:B. Brown Mehlungen AGB. Brown Mehlungen AG Germany

Manufacturer: & nbsp

B. BRAUN MELSUNGEN, AG Germany

Representation: & nbspB. Brown Medikal, Open CompanyB. Brown Medikal, Open Company

Information update date: & nbsp16.06.2018

Illustrated instructions

Instructions

Sodium chloride B. Brown (Sodium chloride B. Braun)