CEFTRIAXONE SODIUM FOR INJECTION POWDER FOR SOLUTION

Quốc gia: Canada

Ngôn ngữ: Tiếng Anh

Nguồn: Health Canada

Thành phần hoạt chất:

CEFTRIAXONE (CEFTRIAXONE SODIUM)

Sẵn có từ:

TEVA CANADA LIMITED

Mã ATC:

J01DD04

INN (Tên quốc tế):

CEFTRIAXONE

Liều dùng:

10G

Dạng dược phẩm:

POWDER FOR SOLUTION

Thành phần:

CEFTRIAXONE (CEFTRIAXONE SODIUM) 10G

Tuyến hành chính:

INTRAMUSCULAR

Các đơn vị trong gói:

101ML

Loại thuốc theo toa:

Prescription

Khu trị liệu:

THIRD GENERATION CEPHALOSPORINS

Tóm tắt sản phẩm:

Active ingredient group (AIG) number: 0117292004; AHFS:

Tình trạng ủy quyền:

APPROVED

Ngày ủy quyền:

2006-11-02

Đặc tính sản phẩm

_PAGE 1 OF 58 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
CEFTRIAXONE SODIUM FOR INJECTION
(STERILE CEFTRIAXONE SODIUM) STERILE POWDER FOR SOLUTION, 1 G AND 10 G CEFTRIAXONE PER VIAL,
INTRAVENOUS OR INTRAMUSCULAR
BP
ANTIBIOTIC
TEVA CANADA LIMITED
30 NOVOPHARM COURT
TORONTO, ONTARIO
M1B 2K9
CONTROL NO: 246728
DATE OF INITIAL
AUTHORIZATION:
NOV. 02, 2006
DATE OF REVISION:
MAY 26, 2021
_PAGE 2 OF 58 _
RECENT MAJOR LABEL CHANGES
WARNINGS AND PRECAUTIONS 04/2020
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
Table of Contents
RECENT MAJOR LABEL CHANGES
.....................................................................................
2
TABLE OF CONTENTS
..........................................................................................................
2
PART I: HEALTH PROFESSIONAL
INFORMATION...............................................................
4
1.
INDICATIONS...............................................................................................................
4
1.1
PEDIATRICS.....................................................................................................................
5
1.2 GERIATRICS
.....................................................................................................................
5
2.
CONTRAINDICATIONS
................................................................................................
5
4.
DOSAGE AND ADMINISTRATION
...............................................................................
5
4.1 DOSING CONSIDERATIONS
................................................................................................
5
4.2 RECOMMENDED DOSE AND DOSAGE
ADJUSTMENT............................................................
5
4.3 RECONSTITUTION
..............................................................................................................
7
4.4
ADMINISTRATION..................................................................................