INJECTABLE ROCURONIUM BROMIDE SOLUTION

Maa: Kanada

Kieli: englanti

Lähde: Health Canada

Osta se nyt

Lataa Valmisteyhteenveto (SPC)
10-07-2023

Aktiivinen ainesosa:

ROCURONIUM BROMIDE

Saatavilla:

OMEGA LABORATORIES LIMITED

ATC-koodi:

M03AC09

INN (Kansainvälinen yleisnimi):

ROCURONIUM BROMIDE

Annos:

10MG

Lääkemuoto:

SOLUTION

Koostumus:

ROCURONIUM BROMIDE 10MG

Antoreitti:

INTRAVENOUS

Kpl paketissa:

100

Prescription tyyppi:

Prescription

Tuoteyhteenveto:

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

Valtuutuksen tilan:

APPROVED

Valtuutus päivämäärä:

2023-07-10

Valmisteyhteenveto

                                _PRODUCT MONOGRAPH: Injectable Rocuronium Bromide _
Page 1 of 33
PRODUCT MONOGRAPH
Pr
INJECTABLE ROCURONIUM BROMIDE
Rocuronium Bromide Injection
10 mg / mL, Solution for Injection, 5 mL vial
Sterile and Preservative Free
Non-depolarizing Skeletal Neuromuscular Blocking Agent
Omega Laboratories Limited
11177 Hamon
Montreal, Canada
H3M 3E4
Date of Preparation:
JUL 10, 2023
Submission Control No.: 276019
_PRODUCT MONOGRAPH: Injectable Rocuronium Bromide _
Page 2 of 33
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
........................................................ 3
SUMMARY PRODUCT INFORMATION
.......................................................................
3
INDICATIONS AND CLINICAL USE
.............................................................................
3
CONTRAINDICATIONS
..................................................................................................
3
WARNINGS AND PRECAUTIONS
.................................................................................
4
ADVERSE REACTIONS
...................................................................................................
8
DRUG INTERACTIONS
.................................................................................................
11
DOSAGE AND ADMINISTRATION
.............................................................................
12
OVERDOSAGE
................................................................................................................
17
ACTION AND CLINICAL PHARMACOLOGY
............................................................ 17
STORAGE AND STABILITY
.........................................................................................
24
SPECIAL HANDLING INSTRUCTIONS
......................................................................
25
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 25
PART II: SCIENTIFIC INFORMATION
..............................................................................
26
PHARMACEUTICAL INFORMATION
....
                                
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Valmisteyhteenveto Valmisteyhteenveto ranska 10-07-2023

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