SMALLPOX VACCINE (DRIED) POWDER FOR SOLUTION

Χώρα: Καναδάς

Γλώσσα: Αγγλικά

Πηγή: Health Canada

Δραστική ουσία:

SMALLPOX VACCINE DRIED

Διαθέσιμο από:

SANOFI PASTEUR LIMITED

Φαρμακολογική κατηγορία (ATC):

J07BX01

INN (Διεθνής Όνομα):

SMALLPOX AND MONKEYPOX VACCINES

Δοσολογία:

100M

Φαρμακοτεχνική μορφή:

POWDER FOR SOLUTION

Σύνθεση:

SMALLPOX VACCINE DRIED 100M

Οδός χορήγησης:

INTRADERMAL

Μονάδες σε πακέτο:

10DOSE

Τρόπος διάθεσης:

Schedule D

Θεραπευτική περιοχή:

VACCINES

Περίληψη προϊόντος:

Active ingredient group (AIG) number: 0106228002; AHFS:

Καθεστώς αδειοδότησης:

CANCELLED POST MARKET

Ημερομηνία της άδειας:

2021-10-05

Αρχείο Π.Χ.Π.

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PACKAGE INSERT
SMALLPOX VACCINE (DRIED)
LIVE VACCINIA VIRUS (BOVINE ORIGIN)
Powder for resuspension
(For active immunization against Smallpox disease)
ATC Code: J07BX Other Viral Vaccines
SANOFI PASTEUR LIMITED
Toronto, Ontario, Canada
Date of Revision:
September 30, 2020
CONTROL#: 243449
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Table of Contents
SUMMARY PRODUCT INFORMATION
........................................................................
3
DESCRIPTION
.....................................................................................................................
3
INDICATIONS AND CLINICAL
USE...............................................................................
3
CONTRAINDICATIONS
.....................................................................................................
4
WARNINGS AND PRECAUTIONS
...................................................................................
5
ADVERSE REACTIONS
.....................................................................................................
6
DRUG INTERACTIONS
.....................................................................................................
9
DOSAGE AND ADMINISTRATION
.................................................................................
9
ACTION AND CLINICAL PHARMACOLOGY
............................................................ 13
STORAGE AND STABILITY
...........................................................................................
14
SPECIAL HANDLING INSTRUCTIONS
.......................................................................
14
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 14
REFERENCES
....................................................................................................................
15
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