NIMBEX LIQUID

Land: Canada

Språk: engelsk

Kilde: Health Canada

Aktiv ingrediens:

CISATRACURIUM (CISATRACURIUM BESYLATE)

Tilgjengelig fra:

ABBVIE CORPORATION

ATC-kode:

M03AC11

INN (International Name):

CISATRACURIUM

Dosering :

2MG

Legemiddelform:

LIQUID

Sammensetning:

CISATRACURIUM (CISATRACURIUM BESYLATE) 2MG

Administreringsrute:

INTRAVENOUS

Enheter i pakken:

10 ML(VIAL)

Resept typen:

Prescription

Terapeutisk område:

NEUROMUSCULAR BLOCKING AGENTS

Produkt oppsummering:

Active ingredient group (AIG) number: 0133260001; AHFS:

Autorisasjon status:

CANCELLED POST MARKET

Autorisasjon dato:

2016-06-07

Preparatomtale

_NIMBEX_
_®_
_ Product Monograph _
_Page 1 of 34 _
PRODUCT MONOGRAPH
PR
NIMBEX
®
cisatracurium besylate injection
solution for injection (2 mg/mL)
Non-depolarizing Skeletal Neuromuscular Blocking Agent
THIS DRUG SHOULD BE ADMINISTERED ONLY BY ADEQUATELY TRAINED
PROFESSIONALS FAMILIAR WITH
ITS ACTIONS, CHARACTERISTICS, AND HAZARDS.
NOTE: NIMBEX
®
is a trademark of the Glaxo group of companies, AbbVie Corporation
licensed use.
_ _
Date of Preparation:
November 1, 2012
AbbVie Corporation
8401 Trans-Canada Highway
St-Laurent, Qc H4S 1Z1
Submission Control No: 158348
_NIMBEX_
_®_
_ Product Monograph _
_Page 2 of 34 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
..........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND PRECAUTIONS
..................................................................................4
ADVERSE REACTIONS
....................................................................................................9
DRUG INTERACTIONS
..................................................................................................11
DOSAGE AND ADMINISTRATION
..............................................................................12
OVERDOSAGE
................................................................................................................18
ACTION AND CLINICAL PHARMACOLOGY
............................................................18
STORAGE AND STABILITY
..........................................................................................26
SPECIAL HANDLING INSTRUCTIONS
.......................................................................26
DOSAGE FORMS, COMPOSITION AND PACKAGING
........................................