Daronrix Ευρωπαϊκή Ένωση - Αγγλικά - EMA (European Medicines Agency)

daronrix

glaxosmithkline biologicals s.a. - whole virion, inactivated, containing antigen*: a/vietnam/1194/2004 (h5n1)* produced in eggs - influenza, human; immunization; disease outbreaks - vaccines - prophylaxis of influenza in an officially declared pandemic situation. pandemic influenza vaccine should be used in accordance with official guidance.

Infanrix Penta Ευρωπαϊκή Ένωση - Αγγλικά - EMA (European Medicines Agency)

infanrix penta

glaxosmithkline biologicals s.a. - diphtheria toxoid, tetanus toxoid, bordetella pertussis antigens (pertussis toxoid, filamentous haemagglutinin, pertactin), poliovirus (inactivated) (type 1 (mahoney strain), type 2 (mef-1 strain), type 3 (saukett strain)), hepatitis b surface antigen - hepatitis b; tetanus; immunization; whooping cough; poliomyelitis; diphtheria - vaccines - infanrix penta is indicated for primary and booster vaccination of infants against diphtheria, tetanus, pertussis, hepatitis b and poliomyelitis.

Twinrix Paediatric Ευρωπαϊκή Ένωση - Αγγλικά - EMA (European Medicines Agency)

twinrix paediatric

glaxosmithkline biologicals s.a. - hepatitis a virus (inactivated), hepatitis b surface antigen - immunization; hepatitis b; hepatitis a - vaccines - twinrix paediatric is indicated for use in non-immune infants, children and adolescents from one year up to and including 15 years who are at risk of both hepatitis-a and hepatitis-b infection.

Pumarix Ευρωπαϊκή Ένωση - Αγγλικά - EMA (European Medicines Agency)

pumarix

glaxosmithkline biologicals s.a.  - pandemic influenza vaccine (h5n1) (split virion, inactivated, adjuvanted)  - influenza, human; immunization; disease outbreaks - vaccines - prophylaxis of influenza in an officially declared pandemic situation.pandemic-influenza vaccine should be used in accordance with official guidance.

Quintanrix Ευρωπαϊκή Ένωση - Αγγλικά - 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 Ευρωπαϊκή Ένωση - Αγγλικά - 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).

Twinrix Adult Ευρωπαϊκή Ένωση - Αγγλικά - EMA (European Medicines Agency)

twinrix adult

glaxosmithkline biologicals s.a. - hepatitis a virus (inactivated), hepatitis b surface antigen - hepatitis b; hepatitis a; immunization - vaccines - twinrix adult is indicated for use in non immune adults and adolescents 16 years of age and above who are at risk of both hepatitis a and hepatitis b infection.

STIEVA-A 0.05% 0.5mg/g cream tube Αυστραλία - Αγγλικά - Department of Health (Therapeutic Goods Administration)

stieva-a 0.05% 0.5mg/g cream tube

glaxosmithkline australia pty ltd - tretinoin, quantity: 0.5 mg/g - cream - excipient ingredients: propylene glycol; purified water; peg-40 stearate; white soft paraffin; propyl hydroxybenzoate; disodium edetate; stearyl alcohol; stearic acid; methyl hydroxybenzoate; butylated hydroxytoluene; isopropyl palmitate; butylated hydroxyanisole - indicated for use in the treatment of acne vulgaris, in particular forms where comedones, papules and pustules predominate.

STIEVA-A 0.025% 0.25mg/g cream tube Αυστραλία - Αγγλικά - Department of Health (Therapeutic Goods Administration)

stieva-a 0.025% 0.25mg/g cream tube

glaxosmithkline australia pty ltd - tretinoin, quantity: 0.25 mg/g - cream - excipient ingredients: methyl hydroxybenzoate; propylene glycol; propyl hydroxybenzoate; white soft paraffin; purified water; stearic acid; peg-40 stearate; butylated hydroxyanisole; butylated hydroxytoluene; stearyl alcohol; isopropyl palmitate; disodium edetate - indicated for use in the treatment of acne vulgaris, in particular forms where comedones, papules and pustules predominate.