MICRO PLUS 4 REGULAR STRENGTH LIQUID

País: Canadá

Língua: inglês

Origem: Health Canada

Ingredientes ativos:

CHROMIUM (CHROMIC CHLORIDE); ZINC (ZINC SULFATE); COPPER (CUPRIC SULFATE); MANGANESE (MANGANESE SULFATE)

Disponível em:

SANDOZ CANADA INCORPORATED

Código ATC:

B05XA31

DCI (Denominação Comum Internacional):

ELECTROLYTES IN COMB WITH OTHER DRUGS

Dosagem:

4MCG; 1MG; .4MG; .1MG

Forma farmacêutica:

LIQUID

Composição:

CHROMIUM (CHROMIC CHLORIDE) 4MCG; ZINC (ZINC SULFATE) 1MG; COPPER (CUPRIC SULFATE) .4MG; MANGANESE (MANGANESE SULFATE) .1MG

Via de administração:

INTRAVENOUS

Unidades em pacote:

10X5ML VIAL

Tipo de prescrição:

Ethical

Área terapêutica:

REPLACEMENT PREPARATIONS

Resumo do produto:

Active ingredient group (AIG) number: 0414689003; AHFS:

Status de autorização:

APPROVED

Data de autorização:

2006-06-07

Características técnicas

_MICRO +4 REGULAR STRENGTH (4 Trace Elements Injection USP) _
_Page 1 of 17 _
_ _
_ _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
MICRO +4 REGULAR STRENGTH
4 Trace Elements Injection
Zinc, 1 mg/mL
Copper, 0.4 mg/mL
Manganese, 0.1 mg/mL
Chromium, 4 mcg/mL
USP
Intravenous
Combination of Electrolytes
Sandoz Canada Inc.
110 Rue de Lauzon
Boucherville, (Québec), Canada
J4B 1K6
Date of Preparation:
APR 25, 1994
Date of Revision:
JAN 19, 2022
Control No.: 250301
_MICRO +4 REGULAR STRENGTH (4 Trace Elements Injection USP) _
_Page 2 of 17 _
RECENT MAJOR LABEL CHANGES
4 DOSAGE AND ADMINISTRATION, 4.2 Recommended Dose and
Dosage Adjustment (Pediatrics)
01/2022
7 WARNINGS AND PRECAUTIONS, General
01/2022
TABLE OF CONTENTS
Sections and Subsections that are not applicable at the time of
authorization are not listed.
PART I: HEALTH PROFESSIONAL INFORMATION
.......................................................................
4
1
INDICATIONS.....................................................................................................................
4
1.1
P
EDIATRICS
(
≤
18 YEARS OF AGE
)
.....................................................................................
4
1.2
G
ERIATRICS
(≥
65 YEARS OF AGE
)
.....................................................................................
4
2
CONTRAINDICATIONS
.......................................................................................................
4
4
DOSAGE AND
ADMINISTRATION........................................................................................
4
4.1
D
OSING
C
ONSIDERATIONS .....................................................................................................
4
4.2
R
ECOMMENDED
D
OSE AND
D
OSAGE
A
DJUSTMENT ......................................................................
5
4.3
R
ECONSTITUTION .................................................................................................................
6
4.4
A
DMINISTRATION ................................................................