TARO-SUNITINIB CAPSULE

País: Canadà

Idioma: anglès

Font: Health Canada

ingredients actius:

SUNITINIB (SUNITINIB MALATE)

Disponible des:

TARO PHARMACEUTICALS INC

Codi ATC:

L01EX01

Designació comuna internacional (DCI):

SUNITINIB

Dosis:

50MG

formulario farmacéutico:

CAPSULE

Composición:

SUNITINIB (SUNITINIB MALATE) 50MG

Vía de administración:

ORAL

Unidades en paquete:

15G/50G

tipo de receta:

Prescription

Resumen del producto:

Active ingredient group (AIG) number: 0151642003; AHFS:

Estat d'Autorització:

APPROVED

Data d'autorització:

2022-01-07

Fitxa tècnica

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_TARO-SUNITINIB Product Monograph _
_ Page 1 of 65_
PRODUCT MONOGRAPH
PR
TARO-SUNITINIB
Sunitinib
Capsules
12.5 mg, 25 mg, 37.5 mg, 50 mg sunitinib
per capsule (as sunitinib
malate)
Tyrosine Kinase Inhibitor, Anti-Tumour Agent
Taro Pharmaceuticals Inc.
130 East Drive
Brampton, ON
L6T 1C1
Date of Preparation:
January 5, 2022
Submission
Control No.: 235867
_Pr_
_TARO-SUNITINIB Product Monograph _
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_Page 2 of 65 _
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....................................................................................................15
DRUG INTERACTIONS
....................................................................................................30
DOSAGE AND ADMINISTRATION
.................................................................................31
OVERDOSAGE
..................................................................................................................32
ACTION AND CLINICAL
PHARMACOLOGY...............................................................32
STORAGE AND STABILITY
............................................................................................36
SPECIAL HANDLING
INSTRUCTIONS..........................................................................36
DOSAGE FORMS, COMPOSITION AND PACKAGING
................................................36
PART II: SCIENTIFIC INFORMATION
.............................................................................37
PHARMACEUTICAL INFORMATION
.............