MORPHINE SULFATE INJECTION USP SOLUTION

Země: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Aktivní složka:

MORPHINE SULFATE

Dostupné s:

PFIZER CANADA ULC

ATC kód:

N02AA01

INN (Mezinárodní Name):

MORPHINE

Dávkování:

2MG

Léková forma:

SOLUTION

Složení:

MORPHINE SULFATE 2MG

Podání:

INTRAMUSCULAR

Jednotky v balení:

10X1 ML

Druh předpisu:

Narcotic (CDSA I)

Terapeutické oblasti:

OPIATE AGONISTS

Přehled produktů:

Active ingredient group (AIG) number: 0104545008; AHFS:

Stav Autorizace:

CANCELLED PRE MARKET

Datum autorizace:

2019-03-04

Charakteristika produktu

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_Product Monograph - _
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_MORPHINE SULFATE INJECTION USP _
_Page 1 of 33 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
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MORPHINE SULFATE INJECTION USP
Sterile Solution
2 mg/mL, 10 mg/mL and 15 mg/mL
Narcotic Analgesic
Pfizer Canada Inc
17300 Trans-Canada Highway
Kirkland, Québec
H9J 2M5
Date of Revision:
October 3, 2018
Submission Control No: 219782
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_Product Monograph - _
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_MORPHINE SULFATE INJECTION USP _
_Page 2 of 33 _
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
..................................................................................................13
DRUG INTERACTIONS
..................................................................................................14
DOSAGE AND ADMINISTRATION
..............................................................................15
OVERDOSAGE
................................................................................................................20
ACTION AND CLINICAL PHARMACOLOGY
............................................................21
STORAGE AND STABILITY
..........................................................................................22
SPECIAL HANDLING INSTRUCTIONS
.......................................................................22
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................22
PART II: SCIENTIFIC INFORMATION
................................................................................24
PHARMACEUTICAL INFORMATION
...................