DUVAXYN EHV 1,4 INACTIVATED ADJUVANTED EQUINE HERPES VACCINE ऑस्ट्रेलिया - अंग्रेज़ी - APVMA (Australian Pesticides and Veterinary Medicines Authority)

duvaxyn ehv 1,4 inactivated adjuvanted equine herpes vaccine

zoetis australia pty ltd - equine herpes virus 1 (ehv-1) 438/77 strain; equine herpes virus 4 (ehv-4) 405/76 strain - parenteral liquid/solution/suspension - equine herpes virus 1 (ehv-1) 438/77 strain vaccine active 0.0 p; equine herpes virus 4 (ehv-4) 405/76 strain vaccine active 0.0 p - immunotherapy - horse | colt | donkey | endurance horse | filly | foal | gelding | high performance horses | horses at stud | mare | pacer | pol - antibiotic - anti-infective | abrasions | abscesses | airsacculitis | antiseptic | avian mycoplasmas | blackhead | body odours | bowed tendons | broad spectrum | burns | coccidiosis | coliform complex | conjunctivitis | cowpox | cracks | crusts | dandruff | dermatological disorders | dermatosis | dry skin | dysentery | eczema | endometritis | enteric diseases | enzootic pneumonia | feed efficiency | fungal infections | girth galls | infections | inflammed pads | itching | keratolytic | lacerations | mastitis | mycoplasmas | odours | open wounds | otitis | pruritis | queensland itch | respiratory disease | saddle rash | salmonellosis | scabs | scaly skin | sheath rot | skin irritations | sores | swine dysentery | teat cracking | teat infections | topical infections | udder sores | weight gain | wire cuts | wounds

CERVARIX human papillomavirus vaccine types 16 and 18 [recombinant, AS04 adjuvanted] suspension for injection vial ऑस्ट्रेलिया - अंग्रेज़ी - Department of Health (Therapeutic Goods Administration)

cervarix human papillomavirus vaccine types 16 and 18 [recombinant, as04 adjuvanted] suspension for injection vial

glaxosmithkline australia pty ltd - hpv type 18 l1 protein, quantity: 20 microgram; hpv type 16 l1 protein, quantity: 20 microgram - injection, suspension - excipient ingredients: water for injections; sodium chloride; 3-o-desacyl-4'-monophosphoryl lipid a; monobasic sodium phosphate; aluminium hydroxide hydrate - cervarix is indicated in females from 10 to 45 years of age for the prevention of persistent infection, premalignant cervical lesions and cervical cancer caused by human papillomavirus types 16 and 18. immunogenicity studies have been conducted in females aged 10 to 14 years and 26 to 45 years to link efficacy in females aged 15 to 25 years to other populations. (see precautions and clinical trials). cervarix is indicated in females from 10 to 45 years for the prevention of cervical cancer by protecting against incident and persistent infections, cytological abnormalities including atypical squamous cells of undetermined significance (asc-us) and cervical intraepithelial neoplasia (cin), cin 1 and pre-cancerous lesions (cin 2 and cin 3) caused by human papillomavirus types 16 and 18. immunogenicity studies have been conducted in females aged 10 to 14 years and 26 to 45 years to link efficacy in females aged 15 to 25 years to other populations.

FLUAD QUAD inactivated quadrivalent influenza vaccine (surface antigen) adjuvanted suspension for injection 60 mcg HA/ 0.5 mL PFS with attached needle, 2024 Season ऑस्ट्रेलिया - अंग्रेज़ी - Department of Health (Therapeutic Goods Administration)

fluad quad inactivated quadrivalent influenza vaccine (surface antigen) adjuvanted suspension for injection 60 mcg ha/ 0.5 ml pfs with attached needle, 2024 season

seqirus pty ltd - influenza virus haemagglutinin, quantity: 15 microgram - injection, suspension - excipient ingredients: monobasic potassium phosphate; magnesium chloride hexahydrate; sorbitan trioleate; squalene; sodium citrate dihydrate; citric acid monohydrate; calcium chloride dihydrate; potassium chloride; water for injections; sodium chloride; dibasic sodium phosphate dihydrate; polysorbate 80 - active immunisation against influenza in persons 65 years of age and older.

FLUAD QUAD inactivated quadrivalent influenza vaccine (surface antigen) adjuvanted suspension for injection 60 mcg HA / 0.5 mL PFS needle-free 2024 Season ऑस्ट्रेलिया - अंग्रेज़ी - Department of Health (Therapeutic Goods Administration)

fluad quad inactivated quadrivalent influenza vaccine (surface antigen) adjuvanted suspension for injection 60 mcg ha / 0.5 ml pfs needle-free 2024 season

seqirus pty ltd - influenza virus haemagglutinin, quantity: 15 microgram - injection, suspension - excipient ingredients: monobasic potassium phosphate; magnesium chloride hexahydrate; sorbitan trioleate; squalene; sodium citrate dihydrate; citric acid monohydrate; calcium chloride dihydrate; potassium chloride; water for injections; sodium chloride; dibasic sodium phosphate dihydrate; polysorbate 80 - active immunisation against influenza in persons 65 years of age and older.

SUVAXYN M HYO आयरलैंड - अंग्रेज़ी - HPRA (Health Products Regulatory Authority)

suvaxyn m hyo

pfizer healthcare ireland - mycoplasma hyopneumoniae strain p-5722-3 - suspension for injection - porcine - immunological - inactivated vaccine

Suvaxyn m hyo आयरलैंड - अंग्रेज़ी - HPRA (Health Products Regulatory Authority)

suvaxyn m hyo

pfizer healthcare ireland - mycoplasma hyopneumoniae strain p-5722-3 - suspension for injection - unknown - immunological - inactivated vaccine - porcine

Prepandrix यूरोपीय संघ - अंग्रेज़ी - EMA (European Medicines Agency)

prepandrix

glaxosmithkline biologicals s.a. - a/indonesia/05/2005 (h5n1) like strain used (pr8-ibcdc-rg2) - influenza, human; immunization; disease outbreaks - vaccines - active immunisation against h5n1 subtype of influenza-a virus.this indication is based on immunogenicity data from healthy subjects from the age of 18 years onwards following administration of two doses of vaccine prepared with h5n1 subtype strains.prepandrix should be used in accordance with official guidance.

Adjupanrix Pandemic Influenza Vaccine (split virion inactivated AS03 adjuvanted) सिंगापुर - अंग्रेज़ी - HSA (Health Sciences Authority)

adjupanrix pandemic influenza vaccine (split virion inactivated as03 adjuvanted)

glaxosmithkline pte ltd - split influenza virus, inactivated, containing antigen eqv a/vietnam/1194/2004 (h5n1) - injection, emulsion - split influenza virus, inactivated, containing antigen eqv a/vietnam/1194/2004 (h5n1) 3.75 µg haemagglutinin/dose

Arexvy यूरोपीय संघ - अंग्रेज़ी - EMA (European Medicines Agency)

arexvy

glaxosmithkline biologicals s.a.  - respiratory syncytial virus recombinant glycoprotein f stabilised in the pre-fusion conformation (rsvpref3) produced in chinese hamster ovary (cho) cells by recombinant dna technology - respiratory syncytial virus infections - vaccines - arexvy is indicated for active immunisation for the prevention of lower respiratory tract disease (lrtd) caused by respiratory syncytial virus in adults 60 years of age and older.the use of this vaccine should be in accordance with official recommendations.