DDAVP MELT TABLET (ORALLY DISINTEGRATING)

Nchi: Kanada

Lugha: Kiingereza

Chanzo: Health Canada

Nunua Sasa

Tabia za bidhaa Tabia za bidhaa (SPC)
31-12-2015

Viambatanisho vya kazi:

DESMOPRESSIN (DESMOPRESSIN ACETATE)

Inapatikana kutoka:

FERRING INC

ATC kanuni:

H01BA02

INN (Jina la Kimataifa):

DESMOPRESSIN

Kipimo:

60MCG

Dawa fomu:

TABLET (ORALLY DISINTEGRATING)

Tungo:

DESMOPRESSIN (DESMOPRESSIN ACETATE) 60MCG

Njia ya uendeshaji:

SUBLINGUAL

Vitengo katika mfuko:

30

Dawa ya aina:

Prescription

Eneo la matibabu:

PITUITARY

Bidhaa muhtasari:

Active ingredient group (AIG) number: 0151664002; AHFS:

Idhini hali ya:

APPROVED

Idhini ya tarehe:

2006-09-08

Tabia za bidhaa

                                _DDAVP® MELT (60μg, 120μg, 240μg) _
_Template Date: January 2010 _
_Page 1 of 34 _
_ _
PRODUCT MONOGRAPH
PR
DDAVP
®
MELT
Desmopressin acetate
60 μg, 120 μg and 240 μg
Oral Disintegrating Tablets
Antidiuretic
Ferring Inc.
200 Yorkland Boulevard
Suite 500
North York, Ontario
M2J 5C1
Date of Revision: DECEMBER 17, 2015.
SUBMISSION CONTROL NO: 187742
_DDAVP® MELT (60μg, 120μg, 240μg) _
_Template Date: January 2010 _
_Page 2 of 34 _
_ _
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
................................................................................9
OVERDOSAGE
................................................................................................................10
ACTION AND CLINICAL PHARMACOLOGY
............................................................11
STORAGE AND STABILITY
..........................................................................................13
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................13
PART II: SCIENTIFIC INFORMATION
................................................................................14
PHARMACEUTICAL INFORMATION
..........................................................................14
CLINICAL TRIALS
...................................
                                
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