ULTRESA CAPSULE (DELAYED RELEASE)

Pays: Canada

Langue: anglais

Source: Health Canada

Ingrédients actifs:

LIPASE; PROTEASE; AMYLASE

Disponible depuis:

APTALIS PHARMA CANADA ULC

Code ATC:

A09AA02

DCI (Dénomination commune internationale):

MULTIENZYMES (LIPASE, PROTEASE ETC)

Dosage:

13800UNIT; 53400UNIT; 58800UNIT

forme pharmaceutique:

CAPSULE (DELAYED RELEASE)

Composition:

LIPASE 13800UNIT; PROTEASE 53400UNIT; AMYLASE 58800UNIT

Mode d'administration:

ORAL

Unités en paquet:

100

Type d'ordonnance:

Prescription

Domaine thérapeutique:

DIGESTANTS

Descriptif du produit:

Active ingredient group (AIG) number: 0302964034; AHFS:

Statut de autorisation:

CANCELLED POST MARKET

Date de l'autorisation:

2016-12-06

Résumé des caractéristiques du produit

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_ULTRESA_
_®_
_ – Pancrelipase Capsules _
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_Page 1 of 18 _
PRODUCT MONOGRAPH
PR
ULTRESA
®
(Pancrelipase USP)
Capsule (Delayed- Release)
13,800, 20,700 and 23,000 USP units of lipase
USP
Pancreatic enzymes
A09AA02
Aptalis Pharma Canada Inc.
597 Sir-Wilfrid-Laurier Blvd.
Mont-Saint-Hilaire, Québec
Canada J3H 6C4
Date of Approval:
June 05, 2015
Submission Control No: 173148
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_ULTRESA_
_®_
_ – Pancrelipase Capsules _
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_Page 2 of 18 _
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
....................................................................................................6
DRUG INTERACTIONS
....................................................................................................8
DOSAGE AND ADMINISTRATION
................................................................................8
OVERDOSAGE
................................................................................................................10
ACTION AND CLINICAL PHARMACOLOGY
............................................................10
STORAGE AND STABILITY
..........................................................................................11
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................11
PART II: SCIENTIFIC INFORMATION
...............................................................................13
PHARMACEUTICAL INFORMATION
..........................................................................13
CLINIC