THROMBATE III POWDER FOR SOLUTION

국가: 캐나다

언어: 영어

출처: Health Canada

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Download 제품 특성 요약 (SPC)
06-10-2016

유효 성분:

ANTITHROMBIN III (HUMAN)

제공처:

GRIFOLS THERAPEUTICS LLC

ATC 코드:

B01AB02

INN (국제 이름):

ANTITHROMBIN

복용량:

1000UNIT

약제 형태:

POWDER FOR SOLUTION

구성:

ANTITHROMBIN III (HUMAN) 1000UNIT

관리 경로:

INTRAVENOUS

패키지 단위:

1000 IU

처방전 유형:

Schedule D

치료 영역:

DIRECT THROMBIN INHIBITORS

제품 요약:

Active ingredient group (AIG) number: 0124256002; AHFS:

승인 상태:

APPROVED

승인 날짜:

2005-06-08

제품 특성 요약

                                _ _
Page 1 of 20
PRODUCT MONOGRAPH
THROMBATE III

Antithrombin III (Human)
I.V. Injection, 500, IU
Manufacturer’s Standard
Anticoagulant
Manufactured by:
Grifols Therapeutics Inc.
8368 US 70 Bus. Hwy West
Clayton, NC 27520
Distributed and Imported by:
Grifols Canada Ltd.
5060 Spectrum Way,
Suite 405
Mississauga, Ontario
L4W 5N5
Submission Control No: 158117 Date of Approval: April 3, 2013
_ _
Page 2 of 20
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
..........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
DESCRIPTION....................................................................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND PRECAUTIONS
..................................................................................4
ADVERSE REACTIONS
....................................................................................................6
DRUG INTERACTIONS
....................................................................................................7
DOSAGE AND ADMINISTRATION
................................................................................8
ACTION AND CLINICAL PHARMACOLOGY
............................................................11
STORAGE AND STABILITY
..........................................................................................12
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................12
PART II: SCIENTIFIC INFORMATION
................................................................................14
PHARMACEUTICAL INFORMATION
..........................................................................14
CLINICAL TRIALS
..................................................................
                                
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