SANDOZ-CALCITONIN NS LIQUID

Land: Canada

Språk: engelsk

Kilde: Health Canada

Aktiv ingrediens:

CALCITONIN (SALMON SYNTHETIC)

Tilgjengelig fra:

SANDOZ CANADA INCORPORATED

ATC-kode:

H05BA01

INN (International Name):

CALCITONIN (SALMON SYNTHETIC)

Dosering :

200UNIT

Legemiddelform:

LIQUID

Sammensetning:

CALCITONIN (SALMON SYNTHETIC) 200UNIT

Administreringsrute:

NASAL

Enheter i pakken:

200 U.I / SPRAY BOTTLE

Resept typen:

Prescription

Terapeutisk område:

PARATHYROID AND ANTIPARATHYROID AGENTS

Produkt oppsummering:

Active ingredient group (AIG) number: 0111011001; AHFS:

Autorisasjon status:

CANCELLED POST MARKET

Autorisasjon dato:

2013-10-01

Preparatomtale

Sandoz Calcitonin NS
Page 1 of 35
PRODUCT MONOGRAPH
PR
SANDOZ CALCITONIN NS
Synthetic Calcitonin (Salmon)
Nasal Spray
200 IU/actuation
Bone Metabolism Regulator
Sandoz Canada Inc.
Date of Revision:
145 Jules-Léger
October 12, 2010
Boucherville, Quebec
J4B-7K8
Control number : 140901
Sandoz Calcitonin NS
Page 2 of 35
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........................................................................................................5
DRUG
INTERACTIONS........................................................................................................10
DOSAGE AND
ADMINISTRATION....................................................................................11
OVERDOSAGE
……………………………………………………………………….........12
ACTION AND CLINICAL
PHARMACOLOGY..................................................................12
STORAGE AND
STABILITY...............................................................................................15
SPECIAL HANDLING
INSTRUCTIONS............................................................................15
DOSAGE FORMS, COMPOSITION AND
PACKAGING..................................................15
PART II: SCIENTIFIC
INFORMATION..........................................................................16
PHARMACEUTICAL
INFORMATION...............................................................................16
CLINICAL
TRIALS....................................................