ЦФД / САГМ - instructions for use, doses, side effects, contraindications

Active substanceAdenine + Dextrose + Citric acid + Mannitol + Sodium dihydrogen phosphate + Sodium citrate + Sodium chlorideAdenine + Dextrose + Citric acid + Mannitol + Sodium dihydrogen phosphate + Sodium citrate + Sodium chloride

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Solutions CFG and SAGM "Terufleks"

solution

ESKOM NPK, OAO Russia

QFD / SAGM

solution

Green Cross Corporation The Republic of Korea

Dosage form: & nbsphemoconvant solution

Composition:

NED

Sodium citrate dihydrate ............ 2.63 g

Citric acid monohydrate ............................ 0.327 g

Sodium dihydrogen phosphate
monohydrate............................. 0.222 g.
Dextrose Monohydrate........... .2.55 grams
SAGM
Sodium chloride ......................... 0,877g
Adenine.........................................0.0169g

Dextrose monohydrate ...............0.900 g

Mannitol ....................................0.525g
water for injections .................up to 100 ml

Description:Transparent, colorless or slightly yellowish liquid.

Pharmacotherapeutic group:Hemoconvant

ATX: & nbsp

V.07.A.C Aids for blood transfusion

Pharmacodynamics:

Hemokonservant has a direct atikoagulantnoe effect. Ensures the preservation of the morphofunctional usefulness of blood, red blood cells during the expiry date for account maintenance of the physiological level of ATP activity in erythrocytes, rheological properties of blood and pH.

Pharmacokinetics:

Indications:

CFD - canning of blood, SAGM - canning of erythrocytes.

Contraindications:

Hypersensitivity

Carefully:not described

Pregnancy and lactation:not described

Dosing and Administration:

The preparation of blood and the production of components from it are carried out in accordance with from "Instructions for the procurement and preservation of blood, approved by the M3 RF on 29.05.1999.

1. Place the container to collect blood and set a zero.

2. Hang the blood collection container below the donor's hand so that the distance between the container and the donor's arm is at least 60 cm.

3. Apply a cuff to measure blood pressure or a tourniquet. Disinfect the venipuncture site. Inflate the cuff to 60 mm Hg. Art. Form a free node) on the donor tube about 10 cm from the needle.

4. Take the donor tube to the clamp.

5. Remove the protective cap from the needle and hold the venipuncture.

6. Loosen the compression cuff, and remove the clamp to begin taking the blood.

7. Stir blood and hemoconvant periodically throughout the blood sampling.

8. Collect blood by weight according to the table.

9. After completing the blood collection, tighten the previously applied knot and remove the needle from the donor's hand.

10. After collecting blood, immediately mix blood with hemoconvant by turning the container several times.

11. Squeeze blood from the donor tube into the container.Shuffle and re-fill donor tube with blood with gemokonservantom.

12. Using a sealer or aluminum rings, seal the donor tube with the numbers. Start sealing the donor tube from the side of the needle, and then from the side of the container.

13. Store the filled container with blood at a temperature of 1-6 ° C.

Side effects:Allergic reactions.

Overdose:

When used in accordance with the instruction, the possibility of adverse reactions is negligible. The most important symptom of overdose is the appearance paresthesia, which requires the cessation or reduction of the rate of administration.

When blood or its components become parasitic, muscle spasms and convulsions in the limbs, it is necessary to immediately stop the injection of blood or its component and prescribe calcium preparations.

Interaction:Incompatible with other medicines.

Special instructions:

Do not use the container if it is damaged or if the solution contained in it is cloudy. If after inspection of the contents of the container it is established that the solution is transparent and contains no particles, the container is checked for leaks, for which it is strongly compressed by hand.When a leak is detected, the container is considered unfit, because its sterility is impaired.

It is necessary to use the containers within 10 days after opening the aluminum foil bag.

Do not use the same system for transfusions of blood components and intravenous infusion of other medicines.

Effect on the ability to drive transp. cf. and fur:not described

Form release / dosage:For 63 ml of CFD and 100 ml of SAGM in blood polymer containers made of polyvinyl chloride (ISO 3826).

Packaging:A constructed container for 450 ml of blood containing 63 ml of CFD, with a 450 ml container containing 100 ml of SAGM, with an empty 300 ml container in the following configuration options:
- with a needle;
- with a needle and adapter for a vacuum tube;
- with a needle, a vacuum tube adapter and a needle protector;
- with a needle, a vacuum tube adapter, a needle protector and a blood sample bag (3 accessories).
A quadruple container for 450 ml of blood containing 63 ml of CFD, with 100 ml of SAGM, two empty containers with a capacity of 300 ml in the following versions:
- with a needle;
- with a needle and adapter for a vacuum tube;
- with a needle, a vacuum tube adapter and a needle protector;
- with a needle, a vacuum tube adapter, a needle protector and a blood sample bag (3 accessories);
A quadruple container for 450 ml of blood containing 63 ml of the CFD, with a 450 ml container containing 100 ml of SAGM, two empty 450 ml containers complete with a needle, a vacuum tube adapter, a needle protector, a blood sample bag and a leukocyte filter 4 accessories).
Each container in the package is packed in an individual transparent polymer bag.
For 4 containers (built with a needle without additional equipment), they are packed in a sealed bag based on aluminum foil. 10 packages with an equal number of instructions for use are placed in a cardboard box.
For 3 containers (built with a needle with optional equipment or quad) is packed in a sealed bag based on aluminum foil. 10 packages with an equal number of instructions for use are placed in a cardboard box.
25 containers (built with 3 accessories) or 20 containers (quad with 3 or 4 accessories) in an individual package are packed in a package based on aluminum foil(non-hermetic) and with an equal number of instructions for use are placed in a cardboard box.

Storage conditions:

In the dark place at a temperature of 2 to 25 ° C.

Shelf life:

3 years (if used as an intermediate secondary packaging hermetically sealed package based on aluminum foil).

2 years (if an unpressurized aluminum foil bag is used as an intermediate secondary packaging).

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

Terms of leave from pharmacies:For hospitals

Registration number:PL-000686

Date of registration:28.09.2011

The owner of the registration certificate:Green Cross CorporationGreen Cross Corporation The Republic of Korea

Manufacturer: & nbsp

Green Cross Medical Science Corporation The Republic of Korea

Information update date: & nbsp19.09.2012

Illustrated instructions

Instructions

QFD / SAGM (CFD / SAGM)