Pentavac Diphtheria, tetanus, pertussis (acellular, component), poliomyelitis (inactivated) and Haemophilus influenzae type b co Írsko - angličtina - HPRA (Health Products Regulatory Authority)

pentavac diphtheria, tetanus, pertussis (acellular, component), poliomyelitis (inactivated) and haemophilus influenzae type b co

sanofi pasteur - purified diphtheria toxoid ph. eur.; purified tetanus toxoid; adsorbed purified pertussis toxoid; adsorbed purified filamentous haemagglutinin; inactivated poliomyelitis virus ph. eur; inactivated type 1 poliovirus; inactivated type 2 poliovirus; inactivated type 3 poliovirus; haemophilus influenzae type b, conjugate with tetanus protein - powder for suspension for injection - 0.5 millilitre(s) - diphtheria-hemophilus influenzae b-pertussis-poliomyelitis-tetanus

DIPHTHERIA AND TETANUS TOXOIDS WITH PERTUSSIS VACCINE ADSORBED LIQUID Kanada - angličtina - Health Canada

diphtheria and tetanus toxoids with pertussis vaccine adsorbed liquid

aventis pasteur limited - diphtheria toxoid; tetanus toxoid; pertussis vaccine - liquid - 25lf; 5lf; 12unit - diphtheria toxoid 25lf; tetanus toxoid 5lf; pertussis vaccine 12unit - toxoids

Diphtheria Tetanus and Pertussis Vaccine Adsorbed Suspension For Injection Keňa - angličtina - Pharmacy and Poisons Board

diphtheria tetanus and pertussis vaccine adsorbed suspension for injection

serum institute of india ltd. 212/2 hadapsar pune 411028 india - diphtheria tetanus and pertussis vaccine adsorbed - suspension for injection - each single 05 ml human dose contains diphtheria… - bacterial vaccines: pertussis vaccines

CSL TETANUS IMMUNOGLOBULIN-VF (human) for intravenous use 4000IU injection vial Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

csl tetanus immunoglobulin-vf (human) for intravenous use 4000iu injection vial

csl behring australia pty ltd - tetanus immunoglobulin, quantity: 4000 iu; human immunoglobulin g, quantity: 50 mg/ml - injection, intravenous infusion - excipient ingredients: maltose; water for injections; human immunoglobulin a - tetanus immunoglobulin-vf (for intravenous use) is used in the management of clinical tetanus.

Adacel Suspension for Injection in pre-filled syringe Malta - angličtina - Medicines Authority

adacel suspension for injection in pre-filled syringe

sanofi pasteur 14 espace henry vallée , 69007 lyon, france - tetanus toxoid, diphtheria toxoid, pertussis toxoid, filamentous haemagglutinin, fha, pertactin, fimbriae types, and, aluminium phosphate - suspension for injection in pre-filled syringe - aluminium phosphate 1.5 mg tetanus toxoid 20 iu diphtheria toxoid 2 iu pertussis toxoid 2.5 µg filamentous haemagglutinin (fha) 5 µg pertactin 3 µg fimbriae types 2 and 3 5 µg - vaccines

Tetanus Immunoglobulin-VF Nový Zéland - angličtina - Medsafe (Medicines Safety Authority)

tetanus immunoglobulin-vf

csl behring (nz) ltd - tetanus immunoglobulin, human 250 [iu] (immunoglobulin ex nz =160mg/ml) - solution for injection - 250 iu - active: tetanus immunoglobulin, human 250 [iu] (immunoglobulin ex nz =160mg/ml) excipient: glycine - tetanus immunoglobulin-vf is indicated for the passive protection of individuals who have sustained a tetanus-prone wound and who have either not been actively immunised against tetanus or whose immunisation history is doubtful. it should also be given to the fully immunised patient with a tetanus-prone wound if more than 10 years have elapsed since the last vaccine dose. in all the above instances, active immunisation with a tetanus vaccine should be commenced at the same time according to current datasheet recommendations.

HYPERTET SD Izrael - angličtina - Ministry of Health

hypertet sd

padagis israel agencies ltd, israel - tetanus immune globulin (s/d treated) - solution for injection - tetanus immune globulin (s/d treated) 250 u/ml - tetanus immunoglobulin - tetanus immunoglobulin - immunity against tetanus toxin. treatment of active cases of tetanus.

Quintanrix Európska únia - angličtina - EMA (European Medicines Agency)

quintanrix

glaxosmithkline biologicals s.a. - diphtheria toxoid, tetanus toxoid, inactivated bordetella pertussis, hepatitis b surface antigen (rdna), haemophilus influenzae type b polysaccharide - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; diphtheria - vaccines - quintanrix is indicated for primary immunisation of infants (during the first year of life) against diphtheria, tetanus, pertussis, hepatitis b and invasive disease caused by haemophilus influenzae type b and for booster immunisation of young children during the second year of life.the use of quintanrix should be determined on the basis of official recommendations.

Tritanrix HepB Európska únia - angličtina - EMA (European Medicines Agency)

tritanrix hepb

glaxosmithkline biologicals s.a. - diphtheria toxoid, hepatitis b surface antigen, bordetella pertussis (inactivated), tetanus toxoid - hepatitis b; tetanus; immunization; whooping cough; diphtheria - vaccines - tritanrix hepb is indicated for active immunisation against diphtheria, tetanus, pertussis and hepatitis b (hbv) in infants from six weeks onwards (see section 4.2).