Valsts: Kanāda
Valoda: angļu
Klimata pārmaiņas: Health Canada
MENINGOCOCCAL GROUP A POLYSACCHARIDE-TETANUS TOXOID CONJUGATE; MENINGOCOCCAL GROUP C POLYSACCHARIDE-TETANUS TOXOID CONJUGATE; MENINGOCOCCAL GROUP Y POLYSACCHARIDE-TETANUS TOXOID CONJUGATE; MENINGOCOCCAL GROUP W POLYSACCHARIDE-TETANUS TOXOID CONJUGATE; TETANUS TOXOID
SANOFI PASTEUR LIMITED
J07AH08
MENINGOCOCCUS, A, C, Y, W-135, TETRAVAL. PURIFIED POLYSACC. ANTIGEN CONJUGATED
10MCG; 10MCG; 10MCG; 10MCG; 55MCG
SOLUTION
MENINGOCOCCAL GROUP A POLYSACCHARIDE-TETANUS TOXOID CONJUGATE 10MCG; MENINGOCOCCAL GROUP C POLYSACCHARIDE-TETANUS TOXOID CONJUGATE 10MCG; MENINGOCOCCAL GROUP Y POLYSACCHARIDE-TETANUS TOXOID CONJUGATE 10MCG; MENINGOCOCCAL GROUP W POLYSACCHARIDE-TETANUS TOXOID CONJUGATE 10MCG; TETANUS TOXOID 55MCG
INTRAMUSCULAR
100
Schedule D
VACCINES
Active ingredient group (AIG) number: 0562558001; AHFS:
APPROVED
2020-10-29
PAGE 1 OF 37 PRODUCT MONOGRAPH INCLUDING PATIENT MEDICATION INFORMATION MENQUADFI ™ Meningococcal (Groups A, C, Y, W) Polysaccharide Tetanus Toxoid Conjugate Vaccine Solution for injection Active Immunizing Agent for the Prevention of Invasive Meningococcal Disease ATC code: J07AH08 Sanofi Pasteur Limited Toronto, Ontario, Canada Date of Approval: October 29, 2020 Submission Control No: 233632 Sanofi Pasteur 395 MenQuadfi TM Product Monograph PAGE 2 OF 37 TABLE OF CONTENTS PART I: HEALTH PROFESSIONAL INFORMATION ........................................................... 4 1 INDICATIONS .................................................................................................................. 4 1.1 Pediatrics ........................................................................................................................... 4 1.2 Geriatrics ........................................................................................................................... 4 2 CONTRAINDICATIONS ................................................................................................ 4 3 DOSAGE AND ADMINISTRATION ............................................................................. 4 3.1 Recommended Dose ......................................................................................................... 4 3.2 Administration .................................................................................................................. 5 4 OVERDOSAGE ................................................................................................................ 5 5 DOSAGE FORMS, STRENGTHS, COMPOSITION AND PACKAGING ............... 5 6 DESCRIPTION ................................................................................................................. 6 7 WARNINGS AND PRECAUTIONS ............................................................................... 7 7.1 Special Populations ................................................................................................... Izlasiet visu dokumentu