STAMARIL, powder and solvent for suspension for injection in  pre-filled syringe.Yellow fever vaccine (Live) Ireland - English - HPRA (Health Products Regulatory Authority)

stamaril, powder and solvent for suspension for injection in pre-filled syringe.yellow fever vaccine (live)

sanofi pasteur - yellow fever virus 17 d-204 strain - powder and solvent for suspension for injection in pre-filled syringe - 1000 international unit(s) - yellow fever vaccines; yellow fever, live attenuated

IMOVAX POLIO, suspension for injection in a prefilled syringe. Poliomyelitis vaccine (inactivated) Malta - English - Medicines Authority

imovax polio, suspension for injection in a prefilled syringe. poliomyelitis vaccine (inactivated)

sanofi pasteur 14 espace henry vallée , 69007 lyon, france - poliovirus, inactivated, type, mahoney strain, mef, saukett strain - suspension for injection - poliovirus (inactivated) type 1 (mahoney strain) 40 dagu poliovirus (inactivated) type 2 (mef-1 strain) 8 dagu poliovirus (inactivated) type 3 (saukett strain) 32 dagu - vaccines

Tetravac, suspension for injection in prefilled syringeDiphtheria, tetanus, pertussis (acellular, component) and poliomyelitis (inactivated) vaccine,(adsorbed). Ireland - English - HPRA (Health Products Regulatory Authority)

tetravac, suspension for injection in prefilled syringediphtheria, tetanus, pertussis (acellular, component) and poliomyelitis (inactivated) vaccine,(adsorbed).

sanofi pasteur - purified tetanus toxoid; purified diphtheria toxoid ph. eur.; 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 - suspension for injection in pre-filled syringe - 0.5 millilitre(s) - bacterial and viral vaccines, combined; diphtheria-pertussis-poliomyelitis-tetanus

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

Pneumo 23 solution for injection in a pre-filled syringe. Polysaccharide pneumococcal vaccine. Malta - English - Medicines Authority

pneumo 23 solution for injection in a pre-filled syringe. polysaccharide pneumococcal vaccine.

sanofi pasteur 14 espace henry vallée , 69007 lyon, france - streptococcus pneumoniae - solution for injection - streptococcus pneumoniae 25 µg - vaccines

TETRACT-HIB, powder and suspension for injection for suspension for injection in prefilled syringe, adsorbed diphtheria, tetanus, pertussis and Haemophilus type b conjugate vaccine. Malta - English - Medicines Authority

tetract-hib, powder and suspension for injection for suspension for injection in prefilled syringe, adsorbed diphtheria, tetanus, pertussis and haemophilus type b conjugate vaccine.

sanofi pasteur 14 espace henry vallée , 69007 lyon, france - tetanus toxoid, diphtheria toxoid, haemophilus type, b polysaccharide, polyribosylribitol phosphate, conjugated to, as carrier, protein, bordetella pertussis - powder and suspension for suspension for injection - diphtheria toxoid haemophilus type b polysaccharide (polyribosylribitol phosphate) conjugated to tetanus toxoid as carrier protein 10 µg bordetella pertussis 4 iu tetanus toxoid 60 iu - vaccines

Rabies Vaccine BP > 2.5 IU/ml, Powder and solvent for suspension for injection Ireland - English - HPRA (Health Products Regulatory Authority)

rabies vaccine bp > 2.5 iu/ml, powder and solvent for suspension for injection

sanofi pasteur - inactivated rabies virus strain pm/wi 38 1503 3m - powder and solvent for suspension for injection - 2.5 international unit(s)/millilitre - rabies vaccines; rabies, inactivated, whole virus

REVAXIS Suspension for injection in pre-filled syringe Diphtheria, tetanus and poliomyelitis (inactivated) vaccine (adsorbed, reduced antigen(s) content) Ireland - English - HPRA (Health Products Regulatory Authority)

revaxis suspension for injection in pre-filled syringe diphtheria, tetanus and poliomyelitis (inactivated) vaccine (adsorbed, reduced antigen(s) content)

sanofi pasteur - diphtheria toxoid; tetanus toxoid; poliovirus, type 1; poliovirus, type 2; poliovirus, type 3 - suspension for injection in pre-filled syringe - 0.5 millilitre(s) - bacterial and viral vaccines, combined; diphtheria-poliomyelitis-tetanus

FLUBLOK QUADRIVALENT NORTHERN HEMISPHERE (influenza a virus a/wisconsin/588/2019 (h1n1) recombinant hemagglutinin antigen, influ United States - English - NLM (National Library of Medicine)

flublok quadrivalent northern hemisphere (influenza a virus a/wisconsin/588/2019 (h1n1) recombinant hemagglutinin antigen, influ

sanofi pasteur inc. - influenza a virus a/wisconsin/588/2019 (h1n1) recombinant hemagglutinin antigen (unii: gb6adz2asn) (influenza a virus a/wisconsin/588/2019 (h1n1) recombinant hemagglutinin antigen - unii:gb6adz2asn), influenza a virus a/darwin/6/2021 (h3n2) recombinant hemagglutinin antigen (unii: 7vj7x8pkx3) (influenza a virus a/darwin/6/2021 (h3n2) recombinant hemagglutinin antigen - unii:7vj7x8pkx3), influenza b virus b/austria/1359417/2021 recombinant hemagglutinin antigen (unii: m48387n67g) (influenza b virus b/aust - flublok quadrivalent is a vaccine indicated for active immunization against disease caused by influenza a subtype viruses and type b viruses contained in the vaccine. flublok quadrivalent is approved for use in persons 18 years of age and older [see clinical studies (14)] . flublok quadrivalent is contraindicated in individuals with known severe allergic reactions (e.g., anaphylaxis) to any component of the vaccine [see postmarketing experience (6.2) and description (11)] . pregnancy exposure pregnancy outcomes in women who have been exposed to flublok quadrivalent during pregnancy are being monitored. sanofi pasteur inc. is maintaining a prospective pregnancy exposure registry to collect data on pregnancy outcomes and newborn health status following vaccination with flublok quadrivalent during pregnancy. healthcare providers are encouraged to enroll women who receive flublok quadrivalent during pregnancy in sanofi pasteur inc.'s vaccination pregnancy registry by calling 1-800-822-2463. risk summary all pre

Typhim VI, solution for injection in a prefilled syringe Polysaccharide typhoid vaccine Malta - English - Medicines Authority

typhim vi, solution for injection in a prefilled syringe polysaccharide typhoid vaccine

sanofi pasteur 14 espace henry vallée , 69007 lyon, france - vi polysaccharide, of salmonella, typhi - solution for injection - vi polysaccharide of salmonella typhi 25 µg - vaccines