Reviews Sodium Acetate Injection


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Sodium Acetate Drug Description
SODIUM ACETATE
(sodium acetate) Injection, Solution, Concentrate
40 mEq (2 mEq/mL)
FOR ADDITIVE USE ONLY AFTER DILUTION IN I.V. FLUIDS.
Plastic Vial
DRUG DESCRIPTION
Sodium Acetate Injection, USP 40 mEq (2 mEq/mL) is a sterile, nonpyrogenic,
concentrated solution of sodium acetate in water for injection. The solution
is administered, after dilution, by the intravenous route as an electrolyte
replenisher. It must not be administered undiluted. Each 20 mL contains 3.28
g of sodium acetate (anhydrous) which provides 40 mEq each of sodium (Na+) and
acetate (CH3COO-). The solution contains no bacteriostat,
antimicrobial agent or added buffer. May contain acetic acid for pH adjustment;
the pH is 6.5 (6.0 to 7.0). The osmolar concentration is 4 mOsmol/mL (calc).
The solution is intended as an alternative to sodium chloride to provide sodium ion (Na+) for addition to large volume infusion fluids for intravenous use.
Sodium Acetate, USP (anhydrous) is chemically designated CH3COONa,
a hygroscopic powder very soluble in water. The semi-rigid container is fabricated
from a specially formulated polyolefin. It is a copolymer of ethylene and propylene.
The safety of the plastic has been confirmed by tests in animals according to
USP biological standards for plastic containers. The container requires no vapor
barrier to maintain the proper drug concentration.Last reviewed on RxList: 5/19/2009




Sodium Acetate Drug Description
SODIUM ACETATE
(sodium acetate) Injection, Solution, Concentrate
40 mEq (2 mEq/mL)
FOR ADDITIVE USE ONLY AFTER DILUTION IN I.V. FLUIDS.
Plastic Vial
DRUG DESCRIPTION
Sodium Acetate Injection, USP 40 mEq (2 mEq/mL) is a sterile, nonpyrogenic,
concentrated solution of sodium acetate in water for injection. The solution
is administered, after dilution, by the intravenous route as an electrolyte
replenisher. It must not be administered undiluted. Each 20 mL contains 3.28
g of sodium acetate (anhydrous) which provides 40 mEq each of sodium (Na+) and
acetate (CH3COO-). The solution contains no bacteriostat,
antimicrobial agent or added buffer. May contain acetic acid for pH adjustment;
the pH is 6.5 (6.0 to 7.0). The osmolar concentration is 4 mOsmol/mL (calc).
The solution is intended as an alternative to sodium chloride to provide sodium ion (Na+) for addition to large volume infusion fluids for intravenous use.
Sodium Acetate, USP (anhydrous) is chemically designated CH3COONa,
a hygroscopic powder very soluble in water. The semi-rigid container is fabricated
from a specially formulated polyolefin. It is a copolymer of ethylene and propylene.
The safety of the plastic has been confirmed by tests in animals according to
USP biological standards for plastic containers. The container requires no vapor
barrier to maintain the proper drug concentration.Last reviewed on RxList: 5/19/2009




Sodium Acetate Drug Description
SODIUM ACETATE
(sodium acetate) Injection, Solution, Concentrate
40 mEq (2 mEq/mL)
FOR ADDITIVE USE ONLY AFTER DILUTION IN I.V. FLUIDS.
Plastic Vial
DRUG DESCRIPTION
Sodium Acetate Injection, USP 40 mEq (2 mEq/mL) is a sterile, nonpyrogenic,
concentrated solution of sodium acetate in water for injection. The solution
is administered, after dilution, by the intravenous route as an electrolyte
replenisher. It must not be administered undiluted. Each 20 mL contains 3.28
g of sodium acetate (anhydrous) which provides 40 mEq each of sodium (Na+) and
acetate (CH3COO-). The solution contains no bacteriostat,
antimicrobial agent or added buffer. May contain acetic acid for pH adjustment;
the pH is 6.5 (6.0 to 7.0). The osmolar concentration is 4 mOsmol/mL (calc).
The solution is intended as an alternative to sodium chloride to provide sodium ion (Na+) for addition to large volume infusion fluids for intravenous use.
Sodium Acetate, USP (anhydrous) is chemically designated CH3COONa,
a hygroscopic powder very soluble in water. The semi-rigid container is fabricated
from a specially formulated polyolefin. It is a copolymer of ethylene and propylene.
The safety of the plastic has been confirmed by tests in animals according to
USP biological standards for plastic containers. The container requires no vapor
barrier to maintain the proper drug concentration.Last reviewed on RxList: 5/19/2009




Sodium Acetate Drug Description
SODIUM ACETATE
(sodium acetate) Injection, Solution, Concentrate
40 mEq (2 mEq/mL)
FOR ADDITIVE USE ONLY AFTER DILUTION IN I.V. FLUIDS.
Plastic Vial
DRUG DESCRIPTION
Sodium Acetate Injection, USP 40 mEq (2 mEq/mL) is a sterile, nonpyrogenic,
concentrated solution of sodium acetate in water for injection. The solution
is administered, after dilution, by the intravenous route as an electrolyte
replenisher. It must not be administered undiluted. Each 20 mL contains 3.28
g of sodium acetate (anhydrous) which provides 40 mEq each of sodium (Na+) and
acetate (CH3COO-). The solution contains no bacteriostat,
antimicrobial agent or added buffer. May contain acetic acid for pH adjustment;
the pH is 6.5 (6.0 to 7.0). The osmolar concentration is 4 mOsmol/mL (calc).
The solution is intended as an alternative to sodium chloride to provide sodium ion (Na+) for addition to large volume infusion fluids for intravenous use.
Sodium Acetate, USP (anhydrous) is chemically designated CH3COONa,
a hygroscopic powder very soluble in water. The semi-rigid container is fabricated
from a specially formulated polyolefin. It is a copolymer of ethylene and propylene.
The safety of the plastic has been confirmed by tests in animals according to
USP biological standards for plastic containers. The container requires no vapor
barrier to maintain the proper drug concentration.Last reviewed on RxList: 5/19/2009




Sodium Acetate Drug Description
SODIUM ACETATE
(sodium acetate) Injection, Solution, Concentrate
40 mEq (2 mEq/mL)
FOR ADDITIVE USE ONLY AFTER DILUTION IN I.V. FLUIDS.
Plastic Vial
DRUG DESCRIPTION
Sodium Acetate Injection, USP 40 mEq (2 mEq/mL) is a sterile, nonpyrogenic,
concentrated solution of sodium acetate in water for injection. The solution
is administered, after dilution, by the intravenous route as an electrolyte
replenisher. It must not be administered undiluted. Each 20 mL contains 3.28
g of sodium acetate (anhydrous) which provides 40 mEq each of sodium (Na+) and
acetate (CH3COO-). The solution contains no bacteriostat,
antimicrobial agent or added buffer. May contain acetic acid for pH adjustment;
the pH is 6.5 (6.0 to 7.0). The osmolar concentration is 4 mOsmol/mL (calc).
The solution is intended as an alternative to sodium chloride to provide sodium ion (Na+) for addition to large volume infusion fluids for intravenous use.
Sodium Acetate, USP (anhydrous) is chemically designated CH3COONa,
a hygroscopic powder very soluble in water. The semi-rigid container is fabricated
from a specially formulated polyolefin. It is a copolymer of ethylene and propylene.
The safety of the plastic has been confirmed by tests in animals according to
USP biological standards for plastic containers. The container requires no vapor
barrier to maintain the proper drug concentration.Last reviewed on RxList: 5/19/2009





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