New Zealand - English - Medsafe (Medicines Safety Authority)

glaxosmithkline nz limited - pneumococcal polysaccharide serotype 1 1ug (conjugated with nthi protein d);  ;  ; pneumococcal polysaccharide serotype 14 1ug (conjugated with nthi protein d);  ;  ; pneumococcal polysaccharide serotype 18c 3ug (conjugated with tetanus toxoid);  ;  ; pneumococcal polysaccharide serotype 19f 3ug (conjugated with diptheria toxoid);  ;  ; pneumococcal polysaccharide serotype 23f 1ug (conjugated with nthi protein d);  ;  ; pneumococcal polysaccharide serotype 4 3ug (conjugated with nthi protein d);  ;  ; pneumococcal polysaccharide serotype 5 1ug (conjugated with nthi protein d);  ;  ; pneumococcal polysaccharide serotype 6b 1ug (conjugated with nthi protein d);  ;  ; pneumococcal polysaccharide serotype 7f 1ug (conjugated with nthi protein d);  ;  ; pneumococcal polysaccharide serotype 9v 1ug (conjugated with nthi protein d);  ;   - suspension for injection - active: pneumococcal polysaccharide serotype 1 1ug (conjugated with nthi protein d)     pneumococcal polysaccharide serotype 14 1ug (conjugated with nthi protein d)     pneumococcal polysaccharide serotype 18c 3ug (conjugated with tetanus toxoid)     pneumococcal polysaccharide serotype 19f 3ug (conjugated with diptheria toxoid)     pneumococcal polysaccharide serotype 23f 1ug (conjugated with nthi protein d)     pneumococcal polysaccharide serotype 4 3ug (conjugated with nthi protein d)     pneumococcal polysaccharide serotype 5 1ug (conjugated with nthi protein d)     pneumococcal polysaccharide serotype 6b 1ug (conjugated with nthi protein d)     pneumococcal polysaccharide serotype 7f 1ug (conjugated with nthi protein d)     pneumococcal polysaccharide serotype 9v 1ug (conjugated with nthi protein d)     excipient: aluminium phosphate diphtheria toxoid, adsorbed haemophilus influenzae protein d sodium chloride tetanus toxoid water for injection - synflorix is indicated for the active immunisation of infants and children from the age of 6 weeks up to 5 years against disease caused by streptococcus pneumoniae vaccine serotypes 1, 4, 5, 6b, 7f, 9v, 14, 18c, 19f, 23f and cross-reactive serotype 19a (including invasive disease, pneumonia and acute otitis media).

New Zealand - English - Medsafe (Medicines Safety Authority)

glaxosmithkline nz limited - hepatitis a vaccine 720 eu/ml;  ; hepatitis b surface antigen, recombinant 20 µg/ml; hepatitis a vaccine 720 eu/ml; hepatitis b surface antigen, recombinant 20 µg/ml - suspension for injection - active: hepatitis a vaccine 720 eu/ml   hepatitis b surface antigen, recombinant 20 µg/ml excipient: aluminium amino acids formaldehyde neomycin sulfate phenoxyethanol polysorbate 20 sodium chloride water for injection active: hepatitis a vaccine 720 eu/ml hepatitis b surface antigen, recombinant 20 µg/ml excipient: aluminium amino acids dibasic sodium phosphate monohydrate formaldehyde monobasic sodium phosphate dihydrate neomycin sulfate polysorbate 20 sodium chloride trometamol water for injection - twinrix is indicated for active immunisation against hepatitis a and hepatitis b virus infection in adults. twinrix is also indicated for active immunisation against hepatitis a and hepatitis b virus infection in infants, children and adolescents from 1 year up to and including 15 years of age at risk of, or who wish to be protected against, both infections.

New Zealand - English - Medsafe (Medicines Safety Authority)

glaxosmithkline nz limited - hepatitis a vaccine 720 eu/ml;  ; hepatitis b surface antigen, recombinant 20 µg/ml; hepatitis a vaccine 720 eu/ml; hepatitis b surface antigen, recombinant 20 µg/ml - suspension for injection - active: hepatitis a vaccine 720 eu/ml   hepatitis b surface antigen, recombinant 20 µg/ml excipient: aluminium amino acids formaldehyde neomycin sulfate phenoxyethanol polysorbate 20 sodium chloride water for injection active: hepatitis a vaccine 720 eu/ml hepatitis b surface antigen, recombinant 20 µg/ml excipient: aluminium amino acids dibasic sodium phosphate monohydrate formaldehyde monobasic sodium phosphate dihydrate neomycin sulfate polysorbate 20 sodium chloride trometamol water for injection - twinrix junior is indicated for active immunisation against hepatitis a and hepatitis b virus infection in infants, children and adolescents from 1 year up to and including 15 years of age at risk of, or who wish to be protected against, both infections.

New Zealand - English - Medsafe (Medicines Safety Authority)

glaxosmithkline nz limited - vi capsular polysaccharide of s. typhi ty2 25ug;   - solution for injection - 25 mcg/0.5ml - active: vi capsular polysaccharide of s. typhi ty2 25ug   excipient: dibasic sodium phosphate dihydrate monobasic sodium phosphate dihydrate phenol sodium chloride water for injection - active immunisation against typhoid fever for adults and children older than two years of age.

New Zealand - English - Medsafe (Medicines Safety Authority)

glaxosmithkline nz limited - varicella vaccine 2000 pfu (not less than); varicella vaccine 2000 pfu (not less than) - powder for injection with diluent - 2000 pfu - active: varicella vaccine 2000 pfu (not less than) excipient: albumin amino acids lactose monohydrate mannitol sorbitol water for injection active: varicella vaccine 2000 pfu (not less than) excipient: amino acids lactose mannitol sorbitol - varilrix is indicated for active immunisation and prophylaxis against varicella in healthy infants (from the age of 9 months), children, adolescents and adults.

Ireland - English - HPRA (Health Products Regulatory Authority)

glaxosmithkline (ireland) limited - polymyxin b sulfate neomycin sulfate hydrocortisone - ear drops suspension - 10000 iu/ml

Ireland - English - HPRA (Health Products Regulatory Authority)

glaxosmithkline (ireland) limited - ondansetron hydrochloride dihydrate - oral solution - 4 mg/5ml

Ireland - English - HPRA (Health Products Regulatory Authority)

glaxosmithkline (ireland) limited - ondansetron hydrochloride - film coated tablet - 4 milligram

Ireland - English - HPRA (Health Products Regulatory Authority)

glaxosmithkline (ireland) limited - ondansetron hydrochloride - film coated tablet - 8 milligram

Singapore - English - HSA (Health Sciences Authority)

glaxosmithkline pte ltd - purified antigen fractions of inactivated split virions - a/indonesia/05/2005 (h5n1)/pr8-ibcdc-rg2 - injection, emulsion - 3.75 µg haemagglutinin/0.25 ml - purified antigen fractions of inactivated split virions - a/indonesia/05/2005 (h5n1)/pr8-ibcdc-rg2 3.75 µg haemagglutinin/0.25 ml