TEVA-EVEROLIMUS TABLET

国家: 加拿大

语言: 英文

来源: Health Canada

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产品特点 产品特点 (SPC)
06-03-2024

有效成分:

EVEROLIMUS

可用日期:

TEVA CANADA LIMITED

ATC代码:

L04AH02

INN(国际名称):

EVEROLIMUS

剂量:

10MG

药物剂型:

TABLET

组成:

EVEROLIMUS 10MG

给药途径:

ORAL

每包单位数:

15G/50G

处方类型:

Prescription

治疗领域:

ANTINEOPLASTIC AGENTS

產品總結:

Active ingredient group (AIG) number: 0152682002; AHFS:

授权状态:

APPROVED

授权日期:

2019-12-06

产品特点

                                _TEVA-EVEROLIMUS_
_ _
Page 1 of 102
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
TEVA-EVEROLIMUS
Everolimus Tablets
Tablets, 2.5 mg, 5 mg, 7.5 mg and 10 mg, Oral
Protein Kinase Inhibitor
ATC Code: L01XE10
Teva Canada Limited
30 Novopharm Court
Toronto, ON
M1B 2K9
Canada
www.tevacanada.com
Date of Initial Authorization:
December 06, 2019
Date of Revision:
MAR 06, 2024
Submission Control Number: 275710
_TEVA-EVEROLIMUS_
_ _
Page 2 of 102
RECENT MAJOR LABEL CHANGES
7 Warning and Precautions, Radiation Sensitization and Radiation
Recall
03/2022
1 Indications, 1.1 Pediatrics
03/2022
3 Serious Warnings and Precautions Box
03/2022
4 Dosage and Administration, 4.1 Dosing Considerations
03/2022
4 Dosage and Administration, 4.4 Administration
03/2022
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL CHANGES
........................................................................................
2
TABLE OF CONTENTS
...........................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
.................................................................. 4
1 INDICATIONS
....................................................................................................................
4
1.1
Pediatrics
...................................................................................................................
5
1.2
Geriatrics
....................................................................................................................
6
2 CONTRAINDICATIONS
......................................................................................................
6
3 SERIOUS WARNINGS AND PRECAUTIONS BOX
................................................................. 6
4 DOSAGE AND ADMINISTRATION
......................................................................................
7
4.1 Dosing Considerations
.......................................
                                
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