01
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solvent for preparing injectable forms
Sodium chloride
solvent for preparing injectable forms
SKU 97184
Same active ingredient
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Manufacturer leaflet
Facts from the printed manufacturer leaflet. Sections vary by drug β we only show what's actually in the box.
Dissolution and dilution of medicinal products.
Π Π°ΡΡΠ²ΠΎΡΠ΅Π½ΠΈΠ΅ ΠΈ ΡΠ°Π·Π²Π΅Π΄Π΅Π½ΠΈΠ΅ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΡ ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΠΎΠ².
Subcutaneously, intramuscularly, intravenously after dissolving or diluting the medicinal products. Preparation of medicinal solutions using sodium chloride is carried out under sterile conditions (opening ampoules, filling syringes and containers with medicinal products). The amount of sodium chloride for preparing the solution of a specific medicinal product is determined by the instructions for use of the product or, depending on the situation, by the physician.
ΠΠΎΠ΄ΠΊΠΎΠΆΠ½ΠΎ, Π²Π½ΡΡΡΠΈΠΌΡΡΠ΅ΡΠ½ΠΎ, Π²Π½ΡΡΡΠΈΠ²Π΅Π½Π½ΠΎ ΠΏΠΎΡΠ»Π΅ ΡΠ°ΡΡΠ²ΠΎΡΠ΅Π½ΠΈΡ ΠΈΠ»ΠΈ ΡΠ°Π·Π²Π΅Π΄Π΅Π½ΠΈΡ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΡ ΡΡΠ΅Π΄ΡΡΠ². ΠΡΠΈΠ³ΠΎΡΠΎΠ²Π»Π΅Π½ΠΈΠ΅ ΡΠ°ΡΡΠ²ΠΎΡΠΎΠ² Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΡ ΡΡΠ΅Π΄ΡΡΠ² Ρ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΠ΅ΠΌ Π½Π°ΡΡΠΈΡ Ρ Π»ΠΎΡΠΈΠ΄Π° ΠΎΡΡΡΠ΅ΡΡΠ²Π»ΡΠ΅ΡΡΡ Π² ΡΡΠ΅ΡΠΈΠ»ΡΠ½ΡΡ ΡΡΠ»ΠΎΠ²ΠΈΡΡ (Π²ΡΠΊΡΡΡΠΈΠ΅ Π°ΠΌΠΏΡΠ», Π½Π°ΠΏΠΎΠ»Π½Π΅Π½ΠΈΠ΅ ΡΠΏΡΠΈΡΠ° ΠΈ Π΅ΠΌΠΊΠΎΡΡΠ΅ΠΉ Ρ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΠΌΠΈ ΡΡΠ΅Π΄ΡΡΠ²Π°ΠΌΠΈ). ΠΠΎΠ»ΠΈΡΠ΅ΡΡΠ²ΠΎ Π½Π°ΡΡΠΈΡ Ρ Π»ΠΎΡΠΈΠ΄Π° Ρ ΡΠ΅Π»ΡΡ ΠΏΡΠΈΠ³ΠΎΡΠΎΠ²Π»Π΅Π½ΠΈΡ ΡΠ°ΡΡΠ²ΠΎΡΠ° ΠΊΠΎΠ½ΠΊΡΠ΅ΡΠ½ΠΎΠ³ΠΎ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΠΎΠ³ΠΎ ΡΡΠ΅Π΄ΡΡΠ²Π° ΠΎΠΏΡΠ΅Π΄Π΅Π»ΡΠ΅ΡΡΡ ΠΈΠ½ΡΡΡΡΠΊΡΠΈΠ΅ΠΉ ΠΏΠΎ ΠΏΡΠΈΠΌΠ΅Π½Π΅Π½ΠΈΡ ΠΏΠΎΡΠ»Π΅Π΄Π½Π΅Π³ΠΎ ΠΈΠ»ΠΈ Π² Π·Π°Π²ΠΈΡΠΈΠΌΠΎΡΡΠΈ ΠΎΡ ΡΠΈΡΡΠ°ΡΠΈΠΈ - Π²ΡΠ°ΡΠΎΠΌ.
1 L of solution contains:
active ingredient: sodium chloride - 9 g,
excipients: water for injections - up to 1 L.
Clear colorless liquid.
1 Π» ΡΠ°ΡΡΠ²ΠΎΡΠ° ΡΠΎΠ΄Π΅ΡΠΆΠΈΡ:
Π°ΠΊΡΠΈΠ²Π½ΠΎΠ΅ Π²Π΅ΡΠ΅ΡΡΠ²ΠΎ: Π½Π°ΡΡΠΈΡ Ρ
Π»ΠΎΡΠΈΠ΄ - 9 Π³,
Π²ΡΠΏΠΎΠΌΠΎΠ³Π°ΡΠ΅Π»ΡΠ½ΠΎΠ΅ Π²Π΅ΡΠ΅ΡΡΠ²ΠΎ: Π²ΠΎΠ΄Π° Π΄Π»Ρ ΠΈΠ½ΡΠ΅ΠΊΡΠΈΠΉ - Π΄ΠΎ 1 Π».
ΠΡΠΎΠ·ΡΠ°ΡΠ½Π°Ρ Π±Π΅ΡΡΠ²Π΅ΡΠ½Π°Ρ ΠΆΠΈΠ΄ΠΊΠΎΡΡΡ.
Do not use for dissolving and diluting medicinal products for which another solvent is specified as mandatory.
Before dissolving/diluting the medicinal product in isotonic sodium chloride solution, carefully read the instructions for use of the medicinal product.
Use only a clear solution, free from visible particles, and if the packaging is undamaged. The solution should be administered using sterile equipment while adhering to aseptic and antiseptic rules. As with all parenteral solutions, the compatibility of added substances with the solution must be determined prior to dissolution. Preparations known to be incompatible with 0.9% sodium chloride solution should not be used with it. The compatibility of added medicinal substances with 0.9% sodium chloride solution must be determined by a physician, checking for possible changes in color and/or the appearance of sediment, insoluble complexes, or crystals. Before adding, it must be determined whether the added substance is soluble and stable in water at the pH level of the 0.9% sodium chloride solution. When adding a preparation, the isotonicity of the resulting solution must be determined before administration. Prior to adding medications to the solution, they must be thoroughly mixed while adhering to aseptic rules. The prepared solution should be administered immediately after preparation; do not store! Do not freeze!
Effect of the preparation on the ability to drive vehicles and operate machinery:
The effect on the ability to perform potentially hazardous activities requiring increased attention and rapid psychomotor reactions (driving vehicles, working with moving machinery) is determined by the pharmacological effects and possible side effects of the primary medicinal product for which sodium chloride is used as a solvent for preparing the injection solution.
ΠΠ΅ ΠΏΡΠΈΠΌΠ΅Π½ΡΡΡ Π΄Π»Ρ ΡΠ°ΡΡΠ²ΠΎΡΠ΅Π½ΠΈΡ ΠΈ ΡΠ°Π·Π²Π΅Π΄Π΅Π½ΠΈΡ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΡ ΡΡΠ΅Π΄ΡΡΠ², Π΄Π»Ρ ΠΊΠΎΡΠΎΡΡΡ Π² ΠΊΠ°ΡΠ΅ΡΡΠ²Π΅ ΠΎΠ±ΡΠ·Π°ΡΠ΅Π»ΡΠ½ΠΎΠ³ΠΎ ΡΠΊΠ°Π·Π°Π½ Π΄ΡΡΠ³ΠΎΠΉ ΡΠ°ΡΡΠ²ΠΎΡΠΈΡΠ΅Π»Ρ.
ΠΠ΅ΡΠ΅Π΄ ΡΠ°ΡΡΠ²ΠΎΡΠ΅Π½ΠΈΠ΅ΠΌ/ΡΠ°Π·Π²Π΅Π΄Π΅Π½ΠΈΠ΅ΠΌ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΠΎΠ³ΠΎ ΡΡΠ΅Π΄ΡΡΠ²Π° Π² ΠΈΠ·ΠΎΡΠΎΠ½ΠΈΡΠ΅ΡΠΊΠΎΠΌ ΡΠ°ΡΡΠ²ΠΎΡΠ΅ Π½Π°ΡΡΠΈΡ Ρ
Π»ΠΎΡΠΈΠ΄Π° ΡΠ»Π΅Π΄ΡΠ΅Ρ Π²Π½ΠΈΠΌΠ°ΡΠ΅Π»ΡΠ½ΠΎ ΠΎΠ·Π½Π°ΠΊΠΎΠΌΠΈΡΡΡΡ Ρ ΠΈΠ½ΡΡΡΡΠΊΡΠΈΠ΅ΠΉ ΠΏΠΎ ΠΏΡΠΈΠΌΠ΅Π½Π΅Π½ΠΈΡ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΠΎΠ³ΠΎ ΡΡΠ΅Π΄ΡΡΠ²Π°.
ΠΡΠΈΠΌΠ΅Π½ΡΡΡ ΡΠΎΠ»ΡΠΊΠΎ ΠΏΡΠΎΠ·ΡΠ°ΡΠ½ΡΠΉ ΡΠ°ΡΡΠ²ΠΎΡ, Π±Π΅Π· Π²ΠΈΠ΄ΠΈΠΌΡΡ
Π²ΠΊΠ»ΡΡΠ΅Π½ΠΈΠΉ ΠΈ, Π΅ΡΠ»ΠΈ ΡΠΏΠ°ΠΊΠΎΠ²ΠΊΠ° Π½Π΅ ΠΏΠΎΠ²ΡΠ΅ΠΆΠ΄Π΅Π½Π°. Π Π°ΡΡΠ²ΠΎΡ ΡΠ»Π΅Π΄ΡΠ΅Ρ Π²Π²ΠΎΠ΄ΠΈΡΡ Ρ ΠΏΡΠΈΠΌΠ΅Π½Π΅Π½ΠΈΠ΅ΠΌ ΡΡΠ΅ΡΠΈΠ»ΡΠ½ΠΎΠ³ΠΎ ΠΎΠ±ΠΎΡΡΠ΄ΠΎΠ²Π°Π½ΠΈΡ Ρ ΡΠΎΠ±Π»ΡΠ΄Π΅Π½ΠΈΠ΅ΠΌ ΠΏΡΠ°Π²ΠΈΠ» Π°ΡΠ΅ΠΏΡΠΈΠΊΠΈ ΠΈ Π°Π½ΡΠΈΡΠ΅ΠΏΡΠΈΠΊΠΈ. ΠΠ°ΠΊ ΠΈ Π΄Π»Ρ Π²ΡΠ΅Ρ
ΠΏΠ°ΡΠ΅Π½ΡΠ΅ΡΠ°Π»ΡΠ½ΡΡ
ΡΠ°ΡΡΠ²ΠΎΡΠΎΠ², ΡΠΎΠ²ΠΌΠ΅ΡΡΠΈΠΌΠΎΡΡΡ Π΄ΠΎΠ±Π°Π²Π»ΡΠ΅ΠΌΡΡ
Π²Π΅ΡΠ΅ΡΡΠ² Ρ ΡΠ°ΡΡΠ²ΠΎΡΠΎΠΌ Π΄ΠΎΠ»ΠΆΠ½Π° ΠΎΠΏΡΠ΅Π΄Π΅Π»ΡΡΡΡΡ ΠΏΠ΅ΡΠ΅Π΄ ΡΠ°ΡΡΠ²ΠΎΡΠ΅Π½ΠΈΠ΅ΠΌ. ΠΠ΅ Π΄ΠΎΠ»ΠΆΠ½Ρ ΠΏΡΠΈΠΌΠ΅Π½ΡΡΡΡΡ Ρ ΡΠ°ΡΡΠ²ΠΎΡΠΎΠΌ Π½Π°ΡΡΠΈΡ Ρ
Π»ΠΎΡΠΈΠ΄Π° 0,9 % ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΡ, ΠΈΠ·Π²Π΅ΡΡΠ½ΡΠ΅ ΠΊΠ°ΠΊ Π½Π΅ΡΠΎΠ²ΠΌΠ΅ΡΡΠΈΠΌΡΠ΅ Ρ Π½ΠΈΠΌ. ΠΠΏΡΠ΅Π΄Π΅Π»ΡΡΡ ΡΠΎΠ²ΠΌΠ΅ΡΡΠΈΠΌΠΎΡΡΡ Π΄ΠΎΠ±Π°Π²Π»ΡΠ΅ΠΌΡΡ
Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΡ
Π²Π΅ΡΠ΅ΡΡΠ² Ρ ΡΠ°ΡΡΠ²ΠΎΡΠΎΠΌ Π½Π°ΡΡΠΈΡ Ρ
Π»ΠΎΡΠΈΠ΄Π° 0,9 % Π΄ΠΎΠ»ΠΆΠ΅Π½ Π²ΡΠ°Ρ, ΠΏΡΠΎΠ²Π΅ΡΠΈΠ² Π²ΠΎΠ·ΠΌΠΎΠΆΠ½ΠΎΠ΅ ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΠ΅ ΠΎΠΊΡΠ°ΡΠΊΠΈ ΠΈ/ΠΈΠ»ΠΈ ΠΏΠΎΡΠ²Π»Π΅Π½ΠΈΠ΅ ΠΎΡΠ°Π΄ΠΊΠ°, Π½Π΅ΡΠ°ΡΡΠ²ΠΎΡΠΈΠΌΡΡ
ΠΊΠΎΠΌΠΏΠ»Π΅ΠΊΡΠΎΠ² ΠΈΠ»ΠΈ ΠΊΡΠΈΡΡΠ°Π»Π»ΠΎΠ². ΠΠ΅ΡΠ΅Π΄ Π΄ΠΎΠ±Π°Π²Π»Π΅Π½ΠΈΠ΅ΠΌ Π½Π΅ΠΎΠ±Ρ
ΠΎΠ΄ΠΈΠΌΠΎ ΠΎΠΏΡΠ΅Π΄Π΅Π»ΠΈΡΡ, ΡΠ²Π»ΡΠ΅ΡΡΡ Π»ΠΈ Π΄ΠΎΠ±Π°Π²Π»ΡΠ΅ΠΌΠΎΠ΅ Π²Π΅ΡΠ΅ΡΡΠ²ΠΎ ΡΠ°ΡΡΠ²ΠΎΡΠΈΠΌΡΠΌ ΠΈ ΡΡΠ°Π±ΠΈΠ»ΡΠ½ΡΠΌ Π² Π²ΠΎΠ΄Π΅ ΠΏΡΠΈ ΡΡΠΎΠ²Π½Π΅ pH, ΡΡΠΎ ΠΈ Ρ ΡΠ°ΡΡΠ²ΠΎΡΠ° Π½Π°ΡΡΠΈΡ Ρ
Π»ΠΎΡΠΈΠ΄Π° 0,9 %. ΠΡΠΈ Π΄ΠΎΠ±Π°Π²Π»Π΅Π½ΠΈΠΈ ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΠ° Π½Π΅ΠΎΠ±Ρ
ΠΎΠ΄ΠΈΠΌΠΎ ΠΎΠΏΡΠ΅Π΄Π΅Π»ΠΈΡΡ ΠΈΠ·ΠΎΡΠΎΠ½ΠΈΡΠ½ΠΎΡΡΡ ΠΏΠΎΠ»ΡΡΠ΅Π½Π½ΠΎΠ³ΠΎ ΡΠ°ΡΡΠ²ΠΎΡΠ° Π΄ΠΎ Π²Π²Π΅Π΄Π΅Π½ΠΈΡ. ΠΠ΅ΡΠ΅Π΄ Π΄ΠΎΠ±Π°Π²Π»Π΅Π½ΠΈΠ΅ΠΌ Π² ΡΠ°ΡΡΠ²ΠΎΡ ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΠΎΠ² ΠΈΡ
Π½Π΅ΠΎΠ±Ρ
ΠΎΠ΄ΠΈΠΌΠΎ ΡΡΠ°ΡΠ΅Π»ΡΠ½ΠΎ ΠΏΠ΅ΡΠ΅ΠΌΠ΅ΡΠ°ΡΡ Ρ ΡΠΎΠ±Π»ΡΠ΄Π΅Π½ΠΈΠ΅ΠΌ ΠΏΡΠ°Π²ΠΈΠ» Π°ΡΠ΅ΠΏΡΠΈΠΊΠΈ. ΠΡΠΈΠ³ΠΎΡΠΎΠ²Π»Π΅Π½Π½ΡΠΉ ΡΠ°ΡΡΠ²ΠΎΡ ΡΠ»Π΅Π΄ΡΠ΅Ρ Π²Π²Π΅ΡΡΠΈ ΡΡΠ°Π·Ρ ΠΏΠΎΡΠ»Π΅ ΠΏΡΠΈΠ³ΠΎΡΠΎΠ²Π»Π΅Π½ΠΈΡ, Π½Π΅ Ρ
ΡΠ°Π½ΠΈΡΡ! ΠΠ΅ Π·Π°ΠΌΠΎΡΠ°ΠΆΠΈΠ²Π°ΡΡ!
ΠΠ»ΠΈΡΠ½ΠΈΠ΅ ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΠ° Π½Π° ΡΠΏΠΎΡΠΎΠ±Π½ΠΎΡΡΡ ΠΊ ΡΠΏΡΠ°Π²Π»Π΅Π½ΠΈΡ ΡΡΠ°Π½ΡΠΏΠΎΡΡΠ½ΡΠΌΠΈ ΡΡΠ΅Π΄ΡΡΠ²Π°ΠΌΠΈ ΠΈ ΠΌΠ΅Ρ
Π°Π½ΠΈΠ·ΠΌΠ°ΠΌΠΈ:
ΠΠ»ΠΈΡΠ½ΠΈΠ΅ Π½Π° ΡΠΏΠΎΡΠΎΠ±Π½ΠΎΡΡΡ ΠΊ Π²ΡΠΏΠΎΠ»Π½Π΅Π½ΠΈΡ ΠΏΠΎΡΠ΅Π½ΡΠΈΠ°Π»ΡΠ½ΠΎ ΠΎΠΏΠ°ΡΠ½ΡΡ
Π²ΠΈΠ΄ΠΎΠ² Π΄Π΅ΡΡΠ΅Π»ΡΠ½ΠΎΡΡΠΈ, ΡΡΠ΅Π±ΡΡΡΠΈΡ
ΠΏΠΎΠ²ΡΡΠ΅Π½Π½ΠΎΠΉ ΠΊΠΎΠ½ΡΠ΅Π½ΡΡΠ°ΡΠΈΠΈ Π²Π½ΠΈΠΌΠ°Π½ΠΈΡ ΠΈ Π±ΡΡΡΡΠΎΡΡ ΠΏΡΠΈΡ
ΠΎΠΌΠΎΡΠΎΡΠ½ΡΡ
ΡΠ΅Π°ΠΊΡΠΈΠΉ (ΡΠΏΡΠ°Π²Π»Π΅Π½ΠΈΠ΅ ΡΡΠ°Π½ΡΠΏΠΎΡΡΠ½ΡΠΌΠΈ ΡΡΠ΅Π΄ΡΡΠ²Π°ΠΌΠΈ, ΡΠ°Π±ΠΎΡΠ° Ρ Π΄Π²ΠΈΠΆΡΡΠΈΠΌΠΈΡΡ ΠΌΠ΅Ρ
Π°Π½ΠΈΠ·ΠΌΠ°ΠΌΠΈ) ΠΎΠΏΡΠ΅Π΄Π΅Π»ΡΠ΅ΡΡΡ ΡΠ°ΡΠΌΠ°ΠΊΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠΈΠΌΠΈ ΡΡΡΠ΅ΠΊΡΠ°ΠΌΠΈ ΠΈ Π²ΠΎΠ·ΠΌΠΎΠΆΠ½ΡΠΌ ΠΏΠΎΠ±ΠΎΡΠ½ΡΠΌ Π΄Π΅ΠΉΡΡΠ²ΠΈΠ΅ΠΌ ΠΎΡΠ½ΠΎΠ²Π½ΠΎΠ³ΠΎ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΠΎΠ³ΠΎ ΡΡΠ΅Π΄ΡΡΠ²Π°, Π΄Π»Ρ ΠΊΠΎΡΠΎΡΠΎΠ³ΠΎ ΠΈΡΠΏΠΎΠ»ΡΠ·ΡΠ΅ΡΡΡ Π½Π°ΡΡΠΈΡ Ρ
Π»ΠΎΡΠΈΠ΄ Π² ΠΊΠ°ΡΠ΅ΡΡΠ²Π΅ ΡΠ°ΡΡΠ²ΠΎΡΠΈΡΠ΅Π»Ρ Π΄Π»Ρ ΠΏΡΠΈΠ³ΠΎΡΠΎΠ²Π»Π΅Π½ΠΈΡ ΡΠ°ΡΡΠ²ΠΎΡΠ° Π΄Π»Ρ ΠΈΠ½ΡΠ΅ΠΊΡΠΈΠΉ.
When using a 0.9% sodium chloride solution as a solvent for medicinal products, the profile of side effects depends on the active pharmaceutical ingredient.
When using a 0.9% sodium chloride solution as a solvent for medicinal products, the symptoms of overdose depend on the active pharmaceutical ingredient.
Compatible with colloidal hemodynamic blood substitutes (mutual enhancement of effect). When mixing with other medications, it is necessary to visually monitor compatibility. For this, it is essential to observe the resulting solution for any changes in color and/or the formation of sediment, appearance of crystals, or insoluble complexes. It is also important to consider the instructions for use of the added medications.
ΠΡΠΈ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΠΈ ΡΠ°ΡΡΠ²ΠΎΡΠ° Π½Π°ΡΡΠΈΡ Ρ Π»ΠΎΡΠΈΠ΄Π° 0,9 % Π² ΠΊΠ°ΡΠ΅ΡΡΠ²Π΅ ΡΠ°ΡΡΠ²ΠΎΡΠΈΡΠ΅Π»Ρ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΡ ΡΡΠ΅Π΄ΡΡΠ², ΠΏΡΠΎΡΠΈΠ»Ρ ΠΏΠΎΠ±ΠΎΡΠ½ΡΡ ΡΡΡΠ΅ΠΊΡΠΎΠ² Π·Π°Π²ΠΈΡΠΈΡ ΠΎΡ ΠΎΡΠ½ΠΎΠ²Π½ΠΎΠ³ΠΎ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΠΎΠ³ΠΎ ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΠ°.
ΠΡΠΈ ΠΏΡΠΈΠΌΠ΅Π½Π΅Π½ΠΈΠΈ ΡΠ°ΡΡΠ²ΠΎΡΠ° Π½Π°ΡΡΠΈΡ Ρ Π»ΠΎΡΠΈΠ΄Π° 0,9 % Π² ΠΊΠ°ΡΠ΅ΡΡΠ²Π΅ ΡΠ°ΡΡΠ²ΠΎΡΠΈΡΠ΅Π»Ρ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΡ ΡΡΠ΅Π΄ΡΡΠ², ΡΠΈΠΌΠΏΡΠΎΠΌΡ ΠΏΠ΅ΡΠ΅Π΄ΠΎΠ·ΠΈΡΠΎΠ²ΠΊΠΈ Π·Π°Π²ΠΈΡΡΡ ΠΎΡ ΠΎΡΠ½ΠΎΠ²Π½ΠΎΠ³ΠΎ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΠΎΠ³ΠΎ ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΠ°.
Π‘ΠΎΠ²ΠΌΠ΅ΡΡΠΈΠΌ Ρ ΠΊΠΎΠ»Π»ΠΎΠΈΠ΄Π½ΡΠΌΠΈ Π³Π΅ΠΌΠΎΠ΄ΠΈΠ½Π°ΠΌΠΈΡΠ΅ΡΠΊΠΈΠΌΠΈ ΠΊΡΠΎΠ²Π΅Π·Π°ΠΌΠ΅Π½ΠΈΡΠ΅Π»ΡΠΌΠΈ (Π²Π·Π°ΠΈΠΌΠ½ΠΎΠ΅ ΡΡΠΈΠ»Π΅Π½ΠΈΠ΅ ΡΡΡΠ΅ΠΊΡΠ°). ΠΡΠΈ ΡΠΌΠ΅ΡΠΈΠ²Π°Π½ΠΈΠΈ Ρ Π΄ΡΡΠ³ΠΈΠΌΠΈ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΠΌΠΈ ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΠ°ΠΌΠΈ Π½Π΅ΠΎΠ±Ρ ΠΎΠ΄ΠΈΠΌΠΎ Π²ΠΈΠ·ΡΠ°Π»ΡΠ½ΠΎ ΠΊΠΎΠ½ΡΡΠΎΠ»ΠΈΡΠΎΠ²Π°ΡΡ ΡΠΎΠ²ΠΌΠ΅ΡΡΠΈΠΌΠΎΡΡΡ. ΠΠ»Ρ ΡΡΠΎΠ³ΠΎ Π½Π΅ΠΎΠ±Ρ ΠΎΠ΄ΠΈΠΌΠΎ Π½Π°Π±Π»ΡΠ΄Π°ΡΡ Π·Π° ΠΏΠΎΠ»ΡΡΠ΅Π½Π½ΡΠΌ ΡΠ°ΡΡΠ²ΠΎΡΠΎΠΌ Π½Π° ΠΏΡΠ΅Π΄ΠΌΠ΅Ρ ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΡ Π΅Π³ΠΎ ΡΠ²Π΅ΡΠ° ΠΈ/ΠΈΠ»ΠΈ Π²ΡΠΏΠ°Π΄Π΅Π½ΠΈΡ ΠΎΡΠ°Π΄ΠΊΠ°, ΠΏΠΎΡΠ²Π»Π΅Π½ΠΈΡ ΠΊΡΠΈΡΡΠ°Π»Π»ΠΎΠ², Π½Π΅ΡΠ°ΡΡΠ²ΠΎΡΠΈΠΌΡΡ ΠΊΠΎΠΌΠΏΠ»Π΅ΠΊΡΠΎΠ². Π’Π°ΠΊΠΆΠ΅ Π½Π΅ΠΎΠ±Ρ ΠΎΠ΄ΠΈΠΌΠΎ ΠΏΡΠΈΠ½ΠΈΠΌΠ°ΡΡ Π²ΠΎ Π²Π½ΠΈΠΌΠ°Π½ΠΈΠ΅ ΠΈΠ½ΡΡΡΡΠΊΡΠΈΠΈ ΠΏΠΎ ΠΏΡΠΈΠΌΠ΅Π½Π΅Π½ΠΈΡ Π΄ΠΎΠ±Π°Π²Π»ΡΠ΅ΠΌΡΡ ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΠΎΠ².
0.9% Sodium Chloride Solution is isotonic with human plasma. In small volumes, it is used as a solvent for the preparation of injectable drug solutions.
Pregnancy and lactation:
The possibility of use during pregnancy and breastfeeding is determined by the instructions for use of the drug for which the 0.9% sodium chloride solution will be used for dilution.
Excreted by the kidneys.
Π Π°ΡΡΠ²ΠΎΡ Π½Π°ΡΡΠΈΡ Ρ
Π»ΠΎΡΠΈΠ΄Π° 0,9 % ΠΈΠ·ΠΎΡΠΎΠ½ΠΈΡΠ΅Π½ ΠΏΠ»Π°Π·ΠΌΠ΅ ΡΠ΅Π»ΠΎΠ²Π΅ΠΊΠ°. Π ΠΌΠ°Π»ΡΡ
ΠΎΠ±ΡΠ΅ΠΌΠ°Ρ
ΠΈΡΠΏΠΎΠ»ΡΠ·ΡΠ΅ΡΡΡ Π² ΠΊΠ°ΡΠ΅ΡΡΠ²Π΅ ΡΠ°ΡΡΠ²ΠΎΡΠΈΡΠ΅Π»Ρ Π΄Π»Ρ ΠΏΡΠΈΠ³ΠΎΡΠΎΠ²Π»Π΅Π½ΠΈΡ ΠΈΠ½ΡΠ΅ΠΊΡΠΈΠΎΠ½Π½ΡΡ
ΡΠ°ΡΡΠ²ΠΎΡΠΎΠ² Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΡ
ΡΡΠ΅Π΄ΡΡΠ².
ΠΠ΅ΡΠ΅ΠΌΠ΅Π½Π½ΠΎΡΡΡ ΠΈ Π»Π°ΠΊΡΠ°ΡΠΈΡ:
ΠΠΎΠ·ΠΌΠΎΠΆΠ½ΠΎΡΡΡ ΠΏΡΠΈΠΌΠ΅Π½Π΅Π½ΠΈΡ ΠΏΡΠΈ Π±Π΅ΡΠ΅ΠΌΠ΅Π½Π½ΠΎΡΡΠΈ ΠΈ Π² ΠΏΠ΅ΡΠΈΠΎΠ΄ Π³ΡΡΠ΄Π½ΠΎΠ³ΠΎ Π²ΡΠΊΠ°ΡΠΌΠ»ΠΈΠ²Π°Π½ΠΈΡ ΠΎΠΏΡΠ΅Π΄Π΅Π»ΡΠ΅ΡΡΡ ΠΈΠ½ΡΡΡΡΠΊΡΠΈΠ΅ΠΉ ΠΏΠΎ ΠΏΡΠΈΠΌΠ΅Π½Π΅Π½ΠΈΡ ΡΠΎΠ³ΠΎ ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΠ°, Π΄Π»Ρ ΡΠ°Π·Π²Π΅Π΄Π΅Π½ΠΈΡ ΠΊΠΎΡΠΎΡΠΎΠ³ΠΎ Π±ΡΠ΄Π΅Ρ ΠΏΡΠΈΠΌΠ΅Π½ΡΡΡΡΡ ΡΠ°ΡΡΠ²ΠΎΡ Π½Π°ΡΡΠΈΡ Ρ
Π»ΠΎΡΠΈΠ΄Π° 0,9 %.
ΠΡΠ²ΠΎΠ΄ΠΈΡΡΡ ΠΏΠΎΡΠΊΠ°ΠΌΠΈ.
RU name ΠΠ°ΡΡΠΈΡ Ρ Π»ΠΎΡΠΈΠ΄ Π±ΡΡΡΡ 0,9% ΡΠ°ΡΡΠ²ΠΎΡΠΈΡΠ΅Π»Ρ Π΄Π»Ρ ΠΏΡΠΈΠ³ΠΎΡΠΎΠ²Π»Π΅Π½ΠΈΡ Π»Π΅ΠΊΠ°ΡΡΡΠ²Π΅Π½Π½ΡΡ ΡΠΎΡΠΌ Π΄Π»Ρ ΠΈΠ½ΡΠ΅ΠΊΡΠΈΠΉ 10 ΠΌΠ» Π°ΠΌΠΏΡΠ»Ρ 10 ΡΡ.
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