REDDY-AZACITIDINE POWDER FOR SUSPENSION

Land: Canada

Taal: Engels

Bron: Health Canada

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Download Productkenmerken (SPC)
26-11-2018

Werkstoffen:

AZACITIDINE

Beschikbaar vanaf:

DR REDDY'S LABORATORIES LTD

ATC-code:

L01BC07

INN (Algemene Internationale Benaming):

AZACITIDINE

Dosering:

100MG

farmaceutische vorm:

POWDER FOR SUSPENSION

Samenstelling:

AZACITIDINE 100MG

Toedieningsweg:

SUBCUTANEOUS

Eenheden in pakket:

30ML

Prescription-type:

Prescription

Therapeutisch gebied:

ANTINEOPLASTIC AGENTS

Product samenvatting:

Active ingredient group (AIG) number: 0152665001; AHFS:

Autorisatie-status:

CANCELLED POST MARKET

Autorisatie datum:

2023-06-27

Productkenmerken

                                1
PRODUCT MONOGRAPH
PR
REDDY-AZACITIDINE
Azacitidine for I
njecti
on
100 mg azacitidine per
vial
Antineoplastic
Agent
Pyrimidine
Analogue
DIN OWNER:
DR. REDDY’S LABORATORIES LIMITED
Bachupally–500 090 INDIA
IMPORTED BY:
DR. REDDY’S LABORATORIES CANADA INC.,
DATE OF REVISION:
2425 Matheson Blvd East, #754
November 26, 2018
Mississauga, ON L4W 5K4 CANADA
Submission Control No: 218731
2
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL
INFORMATION................................................................3
SUMMARY PRODUCT INFORMATION
....................................................................................3
INDICATIONS AND CLINICAL US
E
..........................................................................................3
CONTRAINDICATIONS...............................................................................................................3
WARNINGS AND
PRECAUTIONS..............................................................................................4
ADVERSE
REACTIONS................................................................................................................6
DRUG
INTERACTIONS
..............................................................................................................14
DOSAGE AND
ADMINISTRATION..........................................................................................15
OVERDOSAGE............................................................................................................................19
ACTION AND CLINICAL PHARMACOLOGY
........................................................................19
STORAGE AND
STABILITY......................................................................................................21
SPECIAL HANDLING INSTRUCTIONS
...................................................................................22
DOSAGE FORMS, COMPOSITION AND
PACKAGING.........................................................22
PART II: SCIENTIFIC INFORMATION
................................................
                                
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