SUVAXYN PARVO/E Ireland - English - HPRA (Health Products Regulatory Authority)

suvaxyn parvo/e

zoetis ireland limited - porcine parvovirus, strain s-80 inactivated, erysipelothrix rhusiopathiae suis, strain b-7 (serotype2) inactivated - emulsion for injection - unknown - inactivated porcine parvovirus vaccine + inactivated erysipelothrix vaccine - porcine - immunological - inactivated vaccine

Vaxigrip Tetra Suspension for Injection in Pre-filled Syringe Malaysia - English - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

vaxigrip tetra suspension for injection in pre-filled syringe

sanofi-aventis (malaysia) sdn. bhd. - inactivated,influenza virus type a (h3n2); inactivated,influenza virus type a (h1n1); inactivated,influenza virus type b (b/victoria); inactivated,influenza virus type b (b/yamagata) -

Influvac Tetra suspension for injection in pre-filled syringe Malaysia - English - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

influvac tetra suspension for injection in pre-filled syringe

abbott laboratories (m) sdn. bhd. - inactivated,influenza virus type a (h1n1); inactivated,influenza virus type a (h3n2); inactivated,influenza virus type b (b/yamagata); inactivated,influenza virus type b (b/victoria) -

SKYCellflu Trivalent Solution for Injection in Prefilled Syringe 0.25ml Malaysia - English - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

skycellflu trivalent solution for injection in prefilled syringe 0.25ml

aj biologics sdn. bhd. - inactivated,influenza virus type a (h1n1); inactivated,influenza virus type a (h3n2); inactivated,influenza virus type b (b/victoria) -

SKYCellflu Trivalent Solution for Injection in Prefilled Syringe 0.5ml Malaysia - English - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

skycellflu trivalent solution for injection in prefilled syringe 0.5ml

aj biologics sdn. bhd. - inactivated,influenza virus type a (h1n1); inactivated,influenza virus type a (h3n2); inactivated,influenza virus type b (b/victoria) -

Chick N-K Formulation:   Each 0.1 mL (dose) contains:   Newcastle Disease Virus (B1 Type, La Sota Strain)....>1:32 HI Titer HI – Hemagglutination Inhibition Emulsion for Injection (SC) Philippines - English - FDA (Food And Drug Administration)

chick n-k formulation: each 0.1 ml (dose) contains: newcastle disease virus (b1 type, la sota strain)....>1:32 hi titer hi – hemagglutination inhibition emulsion for injection (sc)

zoetis philippines, inc.; distributor: zoetis philippines, inc. - inactivated newcastle disease (nd) virus vaccine (vet.) - emulsion for injection (sc) - formulation: each 0.1 ml (dose) contains: newcastle disease virus (b1 type, la sota strain)....>1:32 hi titer hi – hemagglutination inhibition

RABAVERT- rabies vaccine kit United States - English - NLM (National Library of Medicine)

rabavert- rabies vaccine kit

a-s medication solutions - rabies virus strain flury lep antigen (propiolactone inactivated) (unii: fk894q51ye) (rabies virus strain flury lep antigen (propiolactone inactivated) - unii:fk894q51ye) - rabavert is indicated for preexposure vaccination, in both primary series and booster dose, and for postexposure prophylaxis against rabies in all age groups. usually an immunization series is initiated and completed with 1 vaccine product. no clinical studies have been conducted that document a change in efficacy or the frequency of adverse reactions when the series is completed with a second vaccine product. however, for booster immunization, rabavert was shown to elicit protective antibody level responses in persons tested who received a primary series with hdcv.4,11 preexposure vaccination: see table 1 and dosage and administration. preexposure vaccination consists of 3 doses of rabavert 1.0 ml given intramuscularly (deltoid region), 1 each on days 0, 7, and 21 or 281 (see also table 1 for criteria for preexposure vaccination). preexposure vaccination does not eliminate the need for additional therapy after a known rabies exposure (see dosage and administration: postexposure prophylaxis of previously im

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

INFANRIX IPV HIB Israel - English - Ministry of Health

infanrix ipv hib

glaxo smith kline (israel) ltd - diphtheria toxoid; fillamentous haemagglutinin (fha); haemophilus influenzae type b polysaccharide; inactivated polio virus (ipv) type 1; inactivated polio virus (ipv) type 2; inactivated polio virus (ipv) type 3; pertactin; pertussis toxoid (pt); tetanus toxoid - powder and suspension for suspension for injection - diphtheria toxoid nlt 60 iu/ml; inactivated polio virus (ipv) type 3 64 du / 1 ml; inactivated polio virus (ipv) type 2 16 du / 1 ml; inactivated polio virus (ipv) type 1 80 du / 1 ml; pertussis toxoid (pt) 50 mcg/ml; fillamentous haemagglutinin (fha) 50 mcg/ml; pertactin 16 mcg/ml; tetanus toxoid nlt 80 iu/ml; haemophilus influenzae type b polysaccharide 20 mcg/vial - diphtheria-hemophilus influenzae b-pertussis-poliomyelitis-tetanus - diphtheria-hemophilus influenzae b-pertussis-poliomyelitis-tetanus - active immunisation in infants from the age of 2 months to 5 years against diptheria, tetanus, pertussis, poliomyelitis and haemophilus influenza type b. booster dose for children who have previously been immunised with dtp, polio and hib antigens