ATROVENT SOLUTION

Land: Canada

Språk: engelsk

Kilde: Health Canada

Aktiv ingrediens:

IPRATROPIUM BROMIDE

Tilgjengelig fra:

BOEHRINGER INGELHEIM (CANADA) LTD LTEE

ATC-kode:

R03BB01

INN (International Name):

IPRATROPIUM BROMIDE

Dosering :

250MCG

Legemiddelform:

SOLUTION

Sammensetning:

IPRATROPIUM BROMIDE 250MCG

Administreringsrute:

INHALATION

Enheter i pakken:

20ML

Resept typen:

Prescription

Terapeutisk område:

ANTIMUSCARINICS ANTISPASMODICS

Produkt oppsummering:

Active ingredient group (AIG) number: 0115643001; AHFS:

Autorisasjon status:

CANCELLED POST MARKET

Autorisasjon dato:

2007-10-11

Preparatomtale

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_Page 1 of 33_
PRODUCT MONOGRAPH
Pr
Atrovent
®
(Ipratropium Bromide)
INHALATION SOLUTION
(20 mL bottle, 1 mL and 2 mL Unit Dose Vials)
BRONCHODILATOR
Boehringer Ingelheim (Canada) Ltd.
5180 South Service Road,
Burlington, Ontario
L7L 5H4
Date of Preparation:
September 19, 2003
Date of Revision:
May 16, 2006
Submission Control No:104456
BICL BPI # 0013-05, #0014-06, #0022-05
_ _
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_Page 2 of 33_
Table of Contents
[To update, right-click anywhere in the Table of Contents and select
“Update Field”, “Update
entire table”, click OK.]
PART I: HEALTH PROFESSIONAL
INFORMATION.........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL
USE..............................................................................3
CONTRAINDICATIONS
...................................................................................................3
WARNINGS AND
PRECAUTIONS..................................................................................4
ADVERSE
REACTIONS....................................................................................................5
DRUG INTERACTIONS
....................................................................................................9
DOSAGE AND
ADMINISTRATION..............................................................................10
OVERDOSAGE
................................................................................................................10
ACTION AND CLINICAL PHARMACOLOGY
............................................................11
STORAGE AND
STABILITY..........................................................................................13
SPECIAL HANDLING INSTRUCTIONS
.......................................................................14
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................14
PART II: SCIENTIFIC INFORMATION
......................................................