ZEMURON SOLUTION

Quốc gia: Canada

Ngôn ngữ: Tiếng Anh

Nguồn: Health Canada

Thành phần hoạt chất:

ROCURONIUM BROMIDE

Sẵn có từ:

MERCK CANADA INC

Mã ATC:

M03AC09

INN (Tên quốc tế):

ROCURONIUM BROMIDE

Liều dùng:

10MG

Dạng dược phẩm:

SOLUTION

Thành phần:

ROCURONIUM BROMIDE 10MG

Tuyến hành chính:

INTRAVENOUS

Các đơn vị trong gói:

10X5ML

Loại thuốc theo toa:

Prescription

Khu trị liệu:

NEUROMUSCULAR BLOCKING AGENTS

Tóm tắt sản phẩm:

Active ingredient group (AIG) number: 0126317001; AHFS:

Tình trạng ủy quyền:

CANCELLED POST MARKET

Ngày ủy quyền:

2018-02-05

Đặc tính sản phẩm

_ _
_Page 1 of 35_
PRODUCT MONOGRAPH
ZEMURON
®
Rocuronium Bromide
10 mg/mL Solution for Injection
_ _
Non-depolarizing Skeletal Neuromuscular Blocking Agent
MERCK CANADA INC.
Date of Revision:
16750 route Transcanadienne
November 5, 2018
Kirkland, QC Canada H9H 4M7
www.merck.ca
Submission Control No: 220017
_ _
_ _
_ _
_ _
_Page 2 of 35_
_ _
TABLE OF CONTENTS
[To create the table of contents, select from the
PART I: HEALTH PROFESSIONAL INFORMATION
..........................................................3
SUMMARY PRODUCT INFORMATION
...............................................................................
3
INDICATIONS AND CLINICAL USE
.....................................................................................
3
CONTRAINDICATIONS
..........................................................................................................
4
WARNINGS AND PRECAUTIONS
.........................................................................................
4
ADVERSE REACTIONS
...........................................................................................................
8
DRUG INTERACTIONS
.........................................................................................................
12
DOSAGE AND ADMINISTRATION
.....................................................................................
13
OVERDOSAGE
.......................................................................................................................
18
ACTION AND CLINICAL PHARMACOLOGY
................................................................... 18
STORAGE AND STABILITY
.................................................................................................
26
SPECIAL HANDLING INSTRUCTIONS
..............................................................................
26
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................................... 26
PART II: SCIENTIFIC INFORMATION
...............................................................................28
PHARMACEUTI