MICAFUNGIN SODIUM FOR INJECTION POWDER FOR SOLUTION

Country: Канада

Језик: Енглески

Извор: Health Canada

Активни састојак:

MICAFUNGIN (MICAFUNGIN SODIUM)

Доступно од:

JUNO PHARMACEUTICALS CORP.

АТЦ код:

J02AX05

INN (Међународно име):

MICAFUNGIN

Дозирање:

50MG

Фармацеутски облик:

POWDER FOR SOLUTION

Састав:

MICAFUNGIN (MICAFUNGIN SODIUM) 50MG

Пут администрације:

INTRAVENOUS

Јединице у пакету:

15G/50G

Тип рецептора:

Prescription

Резиме производа:

Active ingredient group (AIG) number: 0163379001; AHFS:

Статус ауторизације:

APPROVED

Датум одобрења:

2022-02-04

Карактеристике производа

_Product Monograph - Micafungin Sodium for Injection_
_ _
Page 1 of 39_ _
PRODUCT MONOGRAPH
PR
MICAFUNGIN SODIUM FOR INJECTION
50 mg and 100 mg micafungin (as micafungin sodium) per vial
Sterile Powder for Injection
Antifungal
Juno Pharmaceuticals Corp.
402-2233 Argentia Road,
Mississauga, ON L5N 2X7
CONTROL NUMBER: 240052
Date of Preparation:
February 04, 2022
_Product Monograph - Micafungin Sodium for Injection_
_ _
Page 2 of 39_ _
_Product Monograph - Micafungin Sodium for Injection_
_ _
Page 3 of 39_ _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 4
SUMMARY PRODUCT INFORMATION
...................................................................................
4
INDICATIONS AND CLINICAL USE
.........................................................................................
4
CONTRAINDICATIONS
..............................................................................................................
5
WARNINGS AND PRECAUTIONS
.............................................................................................
5
ADVERSE REACTIONS
...............................................................................................................
7
DRUG INTERACTIONS
.............................................................................................................
13
DOSAGE AND ADMINISTRATION
.........................................................................................
14
OVERDOSAGE
...........................................................................................................................
17
ACTION AND CLINICAL PHARMACOLOGY
.......................................................................
18
STORAGE AND STABILITY
.....................................................................................................
21
SPECIAL HANDLING INSTRUCTIONS
..................................................................................
21
DOSAGE FORMS, COMPOSITION AND PACKAGING
....................