ZOLEDRONIC ACID FOR INJECTION CONCENTRATE SOLUTION

Land: Canada

Taal: Engels

Bron: Health Canada

Koop het nu

Productkenmerken Productkenmerken (SPC)
26-02-2014

Werkstoffen:

ZOLEDRONIC ACID (ZOLEDRONIC ACID MONOHYDRATE)

Beschikbaar vanaf:

OMEGA LABORATORIES LIMITED

ATC-code:

M05BA08

INN (Algemene Internationale Benaming):

ZOLEDRONIC ACID

Dosering:

4MG

farmaceutische vorm:

SOLUTION

Samenstelling:

ZOLEDRONIC ACID (ZOLEDRONIC ACID MONOHYDRATE) 4MG

Toedieningsweg:

INTRAVENOUS

Eenheden in pakket:

1VIAL*5ML

Prescription-type:

Prescription

Therapeutisch gebied:

BONE RESORPTION INHIBITORS

Product samenvatting:

Active ingredient group (AIG) number: 0141761002; AHFS:

Autorisatie-status:

APPROVED

Autorisatie datum:

2014-02-26

Productkenmerken

                                PRODUCT MONOGRAPH
PR
Z
OLEDRONIC
A
CID
F
OR
I
NJECTION
C
ONCENTRATE
4 mg/5 mL zoledronic acid (as zoledronic acid monohydrate)
Bone Metabolism Regulator
Omega Laboratories Limited
Date of Preparation: February 18, 2014
11 177 Hamon
Montreal, Quebec
H3M 3E4
Control No. 158614, 171670
_ _
_Page 2 of 58 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY PRODUCT INFORMATION
.......................................................................
3
INDICATIONS AND CLINICAL USE
.............................................................................
3
CONTRAINDICATIONS
..................................................................................................
3
WARNINGS AND PRECAUTIONS
.................................................................................
4
ADVERSE REACTIONS
.................................................................................................
11
DRUG INTERACTIONS
.................................................................................................
22
DOSAGE AND ADMINISTRATION
.............................................................................
22
OVERDOSAGE
................................................................................................................
27
ACTION AND CLINICAL PHARMACOLOGY
........................................................... 27
STORAGE AND STABILITY
.........................................................................................
32
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 32
PART II: SCIENTIFIC INFORMATION
...............................................................................
34
PHARMACEUTICAL INFORMATION
.........................................................................
34
CLINICAL TRIALS
.........................................................................................................
35
DETAILED PHARMACOLOGY
..................................................
                                
                                Lees het volledige document
                                
                            

Documenten in andere talen

Productkenmerken Productkenmerken Frans 04-09-2014

Zoekwaarschuwingen met betrekking tot dit product