FLUDARABINE PHOSPHATE INJECTION, USP SOLUTION

Pajjiż: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ixtrih issa

Ingredjent attiv:

FLUDARABINE PHOSPHATE

Disponibbli minn:

ACCORD HEALTHCARE INC

Kodiċi ATC:

L01BB05

INN (Isem Internazzjonali):

FLUDARABINE

Dożaġġ:

25MG

Għamla farmaċewtika:

SOLUTION

Kompożizzjoni:

FLUDARABINE PHOSPHATE 25MG

Rotta amministrattiva:

INTRAVENOUS

Unitajiet fil-pakkett:

2ML

Tip ta 'preskrizzjoni:

Prescription

Żona terapewtika:

ANTINEOPLASTIC AGENTS

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0123842003; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2015-03-11

Karatteristiċi tal-prodott

                                Page 1 of 55
PRODUCT MONOGRAPH
PR
FLUDARABINE PHOSPHATE INJECTION, USP
Fludarabine Phosphate
Sterile Solution
for Injection
25 mg/mL
(2 mL per vial)
USP
Antineoplastic
Accord Healthcare Inc.
3535 Boulevard St. Charles, Suite 704,
Kirkland, QC,
Canada, H9H 5B9
Date of Revision:
September 29, 2021
Submission
Control No: 253592
Page 2 of 55
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..................................................................................................
9
DRUG INTERACTIONS
.................................................................................................
13
DOSAGE AND
ADMINISTRATION..............................................................................
13
OVERDOSAGE
...............................................................................................................
14
ACTION AND CLINICAL
PHARMACOLOGY............................................................
14
STORAGE AND
STABILITY..........................................................................................
16
SPECIAL HANDLING INSTRUCTIONS
......................................................................
17
DOSAGE FORMS, COMPOSITION AND
PACKAGING............................................. 17
PART II: SCIENTIFIC INFORMATION
...........................................................................
18
PHARMACEUTICAL INFORMATION
........................................................................
18
CLINICAL
TRIALS............................................................
                                
                                Aqra d-dokument sħiħ
                                
                            

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