XIGRIS (5MG/VIAL) POWDER FOR SOLUTION

देश: कनाडा

भाषा: अंग्रेज़ी

स्रोत: Health Canada

इसे खरीदें

सक्रिय संघटक:

DROTRECOGIN ALFA (ACTIVATED)

थमां उपलब्ध:

ELI LILLY CANADA INC

ए.टी.सी कोड:

B01AD10

INN (इंटरनेशनल नाम):

DROTRECOGIN ALFA

डोज़:

5MG

फार्मास्यूटिकल फॉर्म:

POWDER FOR SOLUTION

रचना:

DROTRECOGIN ALFA (ACTIVATED) 5MG

प्रशासन का मार्ग:

INTRAVENOUS

पैकेज में यूनिट:

2.5ML

प्रिस्क्रिप्शन प्रकार:

Prescription

चिकित्सीय क्षेत्र:

OTHER MISCELLANEOUS THERAPEUTIC AGENTS

उत्पाद समीक्षा:

Active ingredient group (AIG) number: 0148944001; AHFS:

प्राधिकरण का दर्जा:

CANCELLED POST MARKET

प्राधिकरण की तारीख:

2011-11-14

उत्पाद विशेषताएं

                                _ _
_XIGRIS [drotrecogin alfa (activated)] _
_Page 1 of 36 _
_Product Monograph _
_ _
PRODUCT MONOGRAPH
Pr
XIGRIS
®
drotrecogin alfa (activated)
Sterile Powder for Intravenous Injection 5 mg or 20 mg drotrecogin
alfa (activated) per vial
ANTITHROMBOTIC PROFIBRINOLYTIC ANTI-INFLAMMATORY ENZYME
©
ELI LILLY CANADA INC.
3650 Danforth Avenue
Toronto, Ontario
M1N 2E8
1-888-545-5972
www.lilly.ca
Date of Approval:
August 20, 2009
Submission Control No: 128989
_ _
_XIGRIS [drotrecogin alfa (activated)] _
_Page 2 of 36 _
_Product Monograph _
_ _
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...................................................................................................
8
DRUG INTERACTIONS
.................................................................................................
12
DOSAGE AND ADMINISTRATION
.............................................................................
13
OVERDOSAGE
...............................................................................................................
16
ACTION AND CLINICAL PHARMACOLOGY
........................................................... 16
STORAGE AND
STABILITY.........................................................................................
19
SPECIAL HANDLING INSTRUCTIONS
......................................................................
19
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 20
PART II: SCIENTIFIC INFORMATION
.............................................
                                
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उत्पाद विशेषताएं उत्पाद विशेषताएं फ़्रेंच 31-08-2009

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