ACTIKERALL SOLUTION

Ország: Kanada

Nyelv: angol

Forrás: Health Canada

Vedd Meg Most

Letöltés Termékjellemzők (SPC)
29-10-2015

Aktív összetevők:

FLUOROURACIL; SALICYLIC ACID

Beszerezhető a:

CIPHER PHARMACEUTICALS INC

ATC-kód:

L01BC52

INN (nemzetközi neve):

FLUOROURACIL, COMBINATIONS

Adagolás:

0.5%; 10%

Gyógyszerészeti forma:

SOLUTION

Összetétel:

FLUOROURACIL 0.5%; SALICYLIC ACID 10%

Az alkalmazás módja:

TOPICAL

db csomag:

25ML

Recept típusa:

Prescription

Terápiás terület:

ANTINEOPLASTIC AGENTS

Termék összefoglaló:

Active ingredient group (AIG) number: 0255930001; AHFS:

Engedélyezési státusz:

APPROVED

Engedély dátuma:

2015-08-27

Termékjellemzők

                                _ _
_ACTIKERALL Product Monograph _
_Page 1 of 26_
PRODUCT MONOGRAPH
PR
ACTIKERALL
TM
fluorouracil and salicylic acid
Solution (0.5%/10%)
Topical Antineoplastic Agent
Cipher Pharmaceuticals Inc.
2345 Argentia Road, Unit 100A
Mississauga, ON
L5N 8K4
Date of Preparation:
August 7, 2015
Submission Control No: 185418
_ _
_ACTIKERALL Product Monograph _
_Page 2 of 26_
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
....................................................................................................6
DRUG INTERACTIONS
....................................................................................................8
DOSAGE AND ADMINISTRATION
................................................................................9
OVERDOSAGE
................................................................................................................11
ACTION AND CLINICAL PHARMACOLOGY
............................................................11
STORAGE AND STABILITY
..........................................................................................13
SPECIAL HANDLING INSTRUCTIONS
.......................................................................13
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................13
PART II: SCIENTIFIC INFORMATION
...............................................................................15
PHARMACEUTICAL INFORMATION
..........................................................................15
CLINICAL TRIALS
...............
                                
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