M-EDIAT CAPSULE (IMMEDIATE RELEASE)

Land: Kanada

Sprache: Englisch

Quelle: Health Canada

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15-08-2018

Wirkstoff:

MORPHINE SULFATE

Verfügbar ab:

ETHYPHARM INC

ATC-Code:

N02AA01

INN (Internationale Bezeichnung):

MORPHINE

Dosierung:

30MG

Darreichungsform:

CAPSULE (IMMEDIATE RELEASE)

Zusammensetzung:

MORPHINE SULFATE 30MG

Verabreichungsweg:

ORAL

Einheiten im Paket:

20/50

Verschreibungstyp:

Narcotic (CDSA I)

Therapiebereich:

OPIATE AGONISTS

Produktbesonderheiten:

Active ingredient group (AIG) number: 0104545011; AHFS:

Berechtigungsstatus:

APPROVED

Berechtigungsdatum:

2008-12-05

Fachinformation

                                _ _
_M-Ediat_
_®_
_ (morphine sulfate immediate release capsules) _
_Page 1 of 36_
PRESCRIBING INFORMATION
INCLUDING PATIENT MEDICATION INFORMATION
N
M-EDIAT
®
Morphine Sulfate Immediate Release Capsules
5 mg, 10 mg, 20 mg and 30 mg
Opioid Analgesic
NOT A PRODUCT MONOGRAPH
Ethypharm Inc.
1000 de la Gauchetière Ouest, Suite 2400
Montréal, Québec
H3B 4W5
Date of Revision:
August 15, 2018
Control No.: 217210
_ _
_M-Ediat_
_®_
_ (morphine sulfate immediate release capsules) _
_Page 2 of 36 _
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
..................................................................................................16
DOSAGE AND ADMINISTRATION
..............................................................................17
OVERDOSAGE
................................................................................................................21
ACTION AND CLINICAL PHARMACOLOGY
............................................................22
STORAGE AND STABILITY
..........................................................................................24
SPECIAL HANDLING INSTRUCTIONS
.......................................................................24
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................25
PART II: SCIENTIFIC INFORMATION
................................................................................26
PHA
                                
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