Sodium Chloride

Quốc gia: New Zealand

Ngôn ngữ: Tiếng Anh

Nguồn: Medsafe (Medicines Safety Authority)

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Thành phần hoạt chất:

Sodium chloride 0.9%

Sẵn có từ:

Baxter Healthcare Ltd

INN (Tên quốc tế):

Sodium chloride 0.9%

Liều dùng:

0.9 %

Dạng dược phẩm:

Solution for infusion

Thành phần:

Active: Sodium chloride 0.9%

Các đơn vị trong gói:

Bag, plastic, 50 mL

Lớp học:

General sale

Loại thuốc theo toa:

General sale

Sản xuất bởi:

Baxter Healthcare Pty Ltd

Chỉ dẫn điều trị:

Sodium chloride (0.9%) intravenous infusion is indicated for extracellular fluid replacement and in the management of metabolic alkalosis in the presence of fluid loss, and for restoring or maintaining the concentration of sodium and chloride ions.

Tóm tắt sản phẩm:

Package - Contents - Shelf Life: Bag, plastic, - 50 mL - 18 months from date of manufacture stored at or below 30°C - Bag, plastic, single - 100 mL - 18 months from date of manufacture stored at or below 30°C - Bag, plastic, double (2 x 100mL) - 200 mL - 24 months from date of manufacture stored at or below 30°C - Bag, plastic, - 250 mL - 24 months from date of manufacture stored at or below 30°C - Bag, plastic, - 500 mL - 24 months from date of manufacture stored at or below 30°C - Bag, plastic, - 1000 mL - 24 months from date of manufacture stored at or below 30°C

Ngày ủy quyền:

1980-10-02

Đặc tính sản phẩm

                                NEW ZEALAND DATA SHEET
Sodium Chloride (Viaflex) Data Sheet 14 August 2019
Page 1 of 11
Baxter Healthcare Ltd
1 Sodium Chloride (infusion, solution)
Sodium Chloride 0.45% Infusion, solution
Sodium Chloride 0.9% Infusion, solution
Sodium Chloride 3% Infusion, solution.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
_Active ingredient _
Sodium chloride, in Water for Injection.
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Infusion, solution in Viaflex plastic bag (for intravenous infusion).
Sodium Chloride infusion solution preparations are sterile,
non‐pyrogenic solutions of sodium chloride
in Water for Injection.
The preparations do not contain an antimicrobial agent or added
buffer, and have a pH of 4.0 – 7.0.
Sodium Chloride 0.9% infusion solution is isotonic, Sodium Chloride 3%
(1026mOsmol/L) is hypertonic
and Sodium Chloride 0.45% (154mOsmol/L) is hypotonic, as indicated by
their osmolarities. The
concentration of sodium chloride in each preparation and their
osmolarities are shown in Table 1 (see
section 6.5). In a dilute condition, osmolarity/L is approximately the
same as osmolality/kg.
4 CLINICAL PARTICULARS
4.1
Therapeutic indications
Sodium Chloride 0.9% infusion solution is indicated for extracellular
fluid replacement and in the
management of metabolic alkalosis in the presence of fluid loss, and
for restoring or maintaining the
concentration of sodium and chloride ions.
Hypertonic Sodium Chloride 3% infusion solution is used in the
management of severe sodium
chloride depletion when electrolyte restoration is required.
Hypotonic Sodium Chloride 0.45% infusion solution is mainly used as a
hydrating agent solution.
4.2
Dose and method of administration
_General directive _
Sodium Chloride (0.45%, 0.9%, 3%) infusion solution is for intravenous
infusion. To be used as
directed by the doctor.
Dosage, rate, and duration of administration are to be individualised
and depend upon the indication
for use, the patient’s age, weight, clinical condition, and
concomitant treatment, and 
                                
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