DAPTOMYCIN FOR INJECTION POWDER FOR SOLUTION

Land: Canada

Språk: engelsk

Kilde: Health Canada

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Last ned Preparatomtale (SPC)
03-05-2019

Aktiv ingrediens:

DAPTOMYCIN

Tilgjengelig fra:

PFIZER CANADA ULC

ATC-kode:

J01XX09

INN (International Name):

DAPTOMYCIN

Dosering :

350MG

Legemiddelform:

POWDER FOR SOLUTION

Sammensetning:

DAPTOMYCIN 350MG

Administreringsrute:

INTRAVENOUS

Enheter i pakken:

1VIAL

Resept typen:

Prescription

Terapeutisk område:

CYCLIC LIPOPEPTIDES

Produkt oppsummering:

Active ingredient group (AIG) number: 0152298002; AHFS:

Autorisasjon status:

CANCELLED PRE MARKET

Autorisasjon dato:

2020-10-16

Preparatomtale

                                PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
DAPTOMYCIN FOR INJECTION
Lyophilized Powder for Solution, For Intravenous Use Only
Daptomycin (350 mg/vial and 500 mg/vial)
Antibacterial Agent
Pfizer Canada ULC
17300 Trans-Canada highway
Kirkland, Québec
H9J 2M5
Submission Control Number: 176067, 211077,
219633, 227098
Date of Preparation:
May 3, 2019
_Product Monograph - Daptomycin for Injection _
_Page 2 of 68 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY PRODUCT INFORMATION
........................................................................
3
INDICATIONS AND CLINICAL USE
..............................................................................
3
CONTRAINDICATIONS
...................................................................................................
5
WARNINGS AND PRECAUTIONS
..................................................................................
5
ADVERSE
REACTIONS..................................................................................................
12
DRUG INTERACTIONS
..................................................................................................
21
DOSAGE AND ADMINISTRATION
..............................................................................
24
OVERDOSAGE
................................................................................................................
30
ACTION AND CLINICAL PHARMACOLOGY
............................................................ 31
STORAGE AND STABILITY
..........................................................................................
36
SPECIAL HANDLING INSTRUCTIONS
.......................................................................
37
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................. 37
PART II: SCIENTIFIC INFORMATION
...............................................................................
38
PHARMACEUTICAL
INFORMATION.................................
                                
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