Diphtheria and Tetanus Vaccine (Adsorbed, Reduced Suspension For Injection Kenya - English - Pharmacy and Poisons Board

diphtheria and tetanus vaccine (adsorbed, reduced suspension for injection

biological e. ltd 18 / 1 & 3, azamabad, hyderabad, telangana - - diphtheria and tetanus vaccine (adsorbed, reduced… - suspension for injection - diphtheria toxoid 2 lf (>/ 2 iu), tetanus toxoid… - tetanus toxoid combinations with diphtheria toxoid

Diphtheria Tetanus and Pertussis Vaccine Adsorbed Suspension For Injection Kenya - English - 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

IMOVAX d.T. adult, suspension for injection in prefilled syringe. Adsorbed diphtheria and tetanus vaccine. Malta - English - Medicines Authority

imovax d.t. adult, suspension for injection in prefilled syringe. adsorbed diphtheria and tetanus vaccine.

sanofi pasteur 14 espace henry vallée , 69007 lyon, france - diphtheria toxoid, tetanus toxoid - suspension for injection - diphtheria toxoid tetanus toxoid - vaccines

ADT BOOSTER diphtheria and tetanus vaccine, adsorbed suspension for injection syringe Australia - English - Department of Health (Therapeutic Goods Administration)

adt booster diphtheria and tetanus vaccine, adsorbed suspension for injection syringe

seqirus pty ltd - diphtheria toxoid, quantity: 4 iu/ml; tetanus toxoid, quantity: 40 iu/ml - injection, suspension - excipient ingredients: water for injections; sodium hydroxide; aluminium hydroxide hydrate; sodium chloride - vaccination of children (greater than or equal to 5 years of age) and adults who have previously received at least 3 doses of a vaccine for primary immunisation against diphtheria and tetanus. adt booster is not intended for primary immunisation against diphtheria and tetanus. use of adt booster should be scheduled in accordance with official national recommendations.

ADT BOOSTER diphtheria and tetanus vaccine, adsorbed suspension for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

adt booster diphtheria and tetanus vaccine, adsorbed suspension for injection vial

seqirus pty ltd - tetanus toxoid, quantity: 40 iu/ml; diphtheria toxoid, quantity: 4 iu/ml - injection, suspension - excipient ingredients: water for injections; sodium chloride; aluminium hydroxide hydrate; sodium hydroxide - vaccination of children (greater than or equal to 5 years of age) and adults who have previously received at least 3 doses of a vaccine for primary immunisation against diphtheria and tetanus. adt booster is not intended for primary immunisation against diphtheria and tetanus. use of adt booster should be scheduled in accordance with official national recommendations.

Diphtheria, Tetanus, Poliomyelitis vaccine, suspension for injection (pre-filled syringe) Malta - English - Medicines Authority

diphtheria, tetanus, poliomyelitis vaccine, suspension for injection (pre-filled syringe)

bilthoven biologicals b.v. antonie van leeuwenhoeklaan 9 3721 ma, bilthoven, netherlands - suspension for injection - diphtheria toxoid >5 iu poliovirus (inactivated) type 1 (mahoney strain) 40 dagu poliovirus (inactivated) type 2 (mef-1 strain) 4 dagu poliovirus (inactivated) type 3 (saukett strain) 7.5 dagu tetanus toxoid >20 iu - vaccines

diTeBooster, suspension for injection in pre-filled single-dose syringes.Diphtheria and tetanus vaccine (adsorbed, reduced antigen content). Ireland - English - HPRA (Health Products Regulatory Authority)

ditebooster, suspension for injection in pre-filled single-dose syringes.diphtheria and tetanus vaccine (adsorbed, reduced antigen content).

aj vaccines a/s - diphtheria toxoid; tetanus toxoid - suspension for injection in pre-filled syringe - . - tetanus vaccines; tetanus toxoid, combinations with diphtheria toxoid

Vaxelis European Union - English - EMA (European Medicines Agency)

vaxelis

mcm vaccine b.v. - diphtheria toxoid, tetanus toxoid, bordetella pertussis antigens: pertussis toxoid, filamentous haemagglutinin, pertactin, fimbriae types 2 and 3, hepatitis b surface antigen produced in yeast cells, poliovirus (inactivated): type 1 (mahoney), type 2 (mef-1), type 3 (saukett) produced in vero cells/ haemophilus influenzae type b polysaccharide (polyribosylribitol phosphate) conjugated to meningococcal protein. - meningitis, haemophilus; poliomyelitis; tetanus; diphtheria; whooping cough; hepatitis b - vaccines - vaxelis (dtap-hb-ipv-hib) is indicated for primary and booster vaccination in infants and toddlers from the age of 6 weeks, against diphtheria, tetanus, pertussis, hepatitis b, poliomyelitis and invasive diseases caused by haemophilus influenzae type b (hib). the use of vaxelis should be in accordance with official recommendations.

Diphtheria, Tetanus, Poliomyelitis vaccine, suspension for injection (vial) Malta - English - Medicines Authority

diphtheria, tetanus, poliomyelitis vaccine, suspension for injection (vial)

bilthoven biologicals b.v. antonie van leeuwenhoeklaan 9 3721 ma, bilthoven, netherlands - suspension for injection - poliovirus (inactivated) type 3 (saukett strain) 7.5 dagu diphtheria toxoid >5 iu tetanus toxoid >20 iu poliovirus (inactivated) type 1 (mahoney strain) 40 dagu poliovirus (inactivated) type 2 (mef-1 strain) 4 dagu - vaccines

Menjugate 10 micrograms suspension for injection Meningococcal group C conjugate vaccine Ireland - English - HPRA (Health Products Regulatory Authority)

menjugate 10 micrograms suspension for injection meningococcal group c conjugate vaccine

gsk vaccines s.r.l. - meningococcal group c oligosaccharide; corynebacterium diphtheriae crm197 protein - suspension for injection in pre-filled syringe - 10 - meningococcal vaccines; other meningococcal polyvalent purified polysaccharides antigen - meningococcal vaccines - active immunisation of children from 2 months of age, adolescents and adults, for the prevention of invasive disease caused by neisseria meningitidis group c.