STAMARIL- yellow fever virus strain 17d-204 live antigen kit United States - English - NLM (National Library of Medicine)

stamaril- yellow fever virus strain 17d-204 live antigen kit

sanofi pasteur inc. - yellow fever virus strain 17d-204 live antigen (unii: py4eet359t) (yellow fever virus strain 17d-204 live antigen - unii:py4eet359t) - yellow fever virus strain 17d-204 live antigen 1000 [iu] in 0.5 ml

JESPECT Japanese encephalitis virus purified inactivated vaccine 0.5mL suspension for injection syringe Australia - English - Department of Health (Therapeutic Goods Administration)

jespect japanese encephalitis virus purified inactivated vaccine 0.5ml suspension for injection syringe

seqirus pty ltd - japanese encephalitis virus, quantity: 6 agu - injection, suspension - excipient ingredients: aluminium hydroxide hydrate; sodium chloride; monobasic potassium phosphate; dibasic sodium phosphate; water for injections - jespect is indicated for active immunisation against japanese encephalitis (je) virus for persons 18 years of age and older. jespect should be considered for use in persons who plan to reside in or travel to areas where je is endemic (common) or epidemic (seasonal), especially during the transmission season. jespect is indicated for persons who work with je virus in laboratories and in industry.

STAMARIL Yellow fever vaccine, live, stabilised   powder for injection vial and diluent syringe Australia - English - Department of Health (Therapeutic Goods Administration)

stamaril yellow fever vaccine, live, stabilised powder for injection vial and diluent syringe

sanofi-aventis australia pty ltd - yellow fever virus, quantity: 1000 pfu e.1000 mouse ld50 - injection, powder for - excipient ingredients: calcium chloride dihydrate; magnesium sulfate heptahydrate; histidine hydrochloride; sodium chloride; dibasic sodium phosphate dihydrate; alanine; sorbitol; potassium chloride; lactose monohydrate; monobasic potassium phosphate; sodium hydroxide - prevention of yellow fever. vaccination is recommended for:,? every individual aged 9 months and over living or travelling through an endemic area with a current or periodic risk of yellow fever transmission. ? non-vaccinated individual moving from an endemic area with a current or periodic risk of yellow fever transmission to a potentially receptive non-endemic area with a current or periodic risk of yellow fever transmission. ? laboratory workers handling potentially infectious materials. in order to be officially recognised, the yellow fever vaccination must be administered in an approved vaccination centre and registered on an international certificate. the validity period of the certificate is established according to international health regulations recommendations and starts 10 days after primary vaccination and immediately after re-vaccination.

DENGVAXIA POLVO Y DISOLVENTE PARA SUSPENSIÓN INYECTABLE MULTIDOSIS (VACUNA TETRAVALENTE CONTRA EL DENGUE DE VIRUS ATENUADOS) Panama - English - Ministerio de Salud (Dirección Nacional de Farmacia Y Drogas)

dengvaxia polvo y disolvente para suspensión inyectable multidosis (vacuna tetravalente contra el dengue de virus atenuados)

sanofi pasteur - virus cyd del dengue serotipo 1 - virus cyd del dengue serotipo 1....4,5-6 log10 ccid50/dosisi / virus cyd del dengue serotipo 2 ....4,5-6 log10 ccid50/dosisi / virus cyd del dengue serotipo 3....4,5-6 log10 ccid50/dosisi / virus cyd del dengue serotipo 4....4,5-6 log10 ccid50/dosisi / cloruro de sodio....0.9%

DENGVAXIA POLVO Y DISOLVENTE PARA SUSPENSIÓN INYECTABLE UNIDOSIS (VACUNA TETRAVALENTE CONTRA EL DENGUE DE VIRUS ATENUADOS) Panama - English - Ministerio de Salud (Dirección Nacional de Farmacia Y Drogas)

dengvaxia polvo y disolvente para suspensión inyectable unidosis (vacuna tetravalente contra el dengue de virus atenuados)

sanofi pasteur - virus cyd del dengue serotipo 1 - virus cyd del dengue serotipo 1....4,5-6 log10 ccid50/dosisi / virus cyd del dengue serotipo 2 ....4,5-6 log10 ccid50/dosisi / virus cyd del dengue serotipo 3....4,5-6 log10 ccid50/dosisi / virus cyd del dengue serotipo 4....4,5-6 log10 ccid50/dosisi / cloruro de sodio....2 mg

Stamaril Powder+Solvent for Susp for Injection in pre-filled syringe, Yellow fever vaccine (Live) Malta - English - Medicines Authority

stamaril powder+solvent for susp for injection in pre-filled syringe, yellow fever vaccine (live)

sanofi pasteur 14 espace henry vallée , 69007 lyon, france - yellow fever, virus strain, d - powder and solvent for suspension for injection - yellow fever virus strain 17d 1000 iu - vaccines

TicoVac  0.5ml pre-filled syringe/Tick-Borne Encephalitis Vaccine (Whole Virus, inactivated) Malta - English - Medicines Authority

ticovac 0.5ml pre-filled syringe/tick-borne encephalitis vaccine (whole virus, inactivated)

pfizer hellas s.a. 243 messoghion ave., neo psychiko 15451, athens, greece - tick, borne encephalitis, virus - suspension for injection in pre-filled syringe - tick-borne encephalitis virus 1,2 0.5 ml - vaccines

Stamaril New Zealand - English - Medsafe (Medicines Safety Authority)

stamaril

pharmacy retailing (nz) ltd t/a healthcare logistics - yellow fever vaccine 1000 [iu] (17d strain);   - suspension for injection - 1000 iu - active: yellow fever vaccine 1000 [iu] (17d strain)   excipient: alanine calcium chloride dihydrate dibasic sodium phosphate dihydrate histidine hydrochloride lactose monohydrate magnesium sulfate heptahydrate monobasic potassium phosphate potassium chloride sodium chloride sodium hydroxide sorbitol purified water sodium chloride - prevention of yellow fever. vaccination is recommended for: · every person over 9 months of age living or travelling through an endemic area. · non-vaccinated persons moving from an endemic to a potentially receptive non-endemic area. · laboratory workers handling potentially infectious materials. · in order to be officially recognised, the yellow fever vaccination must be administered in an approved vaccination centre and registered on an international certificate. the validity period of the certificate is established according to international health regulations recommendations and starts 10 days after primary vaccination and immediately after re-vaccination.

STAMARIL YELLOW FEVER VACCINE 1000 Suspension for Injection Ireland - English - HPRA (Health Products Regulatory Authority)

stamaril yellow fever vaccine 1000 suspension for injection

sanofi pasteur msd ltd - yellow fever virus 17 d-204 strain - suspension for injection - 1000 - yellow fever vaccines

IMOVAX RABIES POWDER FOR SUSPENSION Canada - English - Health Canada

imovax rabies powder for suspension

sanofi pasteur limited - rabies vaccine inactivated (human diploid-cell culture) - powder for suspension - 2.5unit - rabies vaccine inactivated (human diploid-cell culture) 2.5unit - vaccines