European Union - English - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - vcp65 virus - immunologicals - cats - active immunisation of cats 12 weeks of age and older to prevent mortality due to rabies infection.onset of immunity: 4 weeks after the primary vaccination course.duration of immunity after primary vaccination: 1 year.duration of immunity after revaccination: 3 years.

Ireland - English - HPRA (Health Products Regulatory Authority)

intervet ireland limited - inactivated rabies virus antigen suspension - suspension for injection - 2-6 international units/dose - rabies virus - cats, dogs - immunological - inactivated vaccine

New Zealand - English - Medsafe (Medicines Safety Authority)

seqirus (nz) ltd - rabies vaccine 2.5 [iu] - injection with diluent - 2.5 iu - active: rabies vaccine 2.5 [iu] excipient: disodium edetate potassium l-glutamate polygeline sodium chloride sucrose trometamol water for injection - active immunisation against rabies virus, including (a) pre-exposure immunisation, (b) post-exposure treatment following exposure to rabies virus

India - English - Central Drugs Standard Control Organization

gen bio. - rabies immunoglobulin - vaccine - anti rabies serum - single dose via syringe diluent

India - English - Central Drugs Standard Control Organization

ranbaxy - rabies immunoglobulin - 300iu. (human rabies ig 300iu.) - 2ml

Australia - English - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - rabies virus -

Israel - English - Ministry of Health

csl behring ltd., israel - human-rabies immunoglobulin - solution for injection - human-rabies immunoglobulin 150 iu/ml - rabies immunoglobulin - rabies immunoglobulin - prophylaxis of rabies.

Philippines - English - FDA (Food And Drug Administration)

msd animal health (phils.), inc.; distributor: msd animal health (phils.), inc. - inactivated rabies virus vaccine (vet.) - suspension for injection (sc/im) - formulation: each 1 ml (dose) contains: rabies virus (pasteur riv strain).............. > 2i.u. iu-international units

Australia - English - Department of Health (Therapeutic Goods Administration)

link medical products pty ltd t/a link pharmaceuticals - rabies immunoglobulin, quantity: 150 iu/ml - injection, solution - excipient ingredients: sodium hydroxide; glycine; water for injections - kamrab is rabies immunoglobulin indicated for passive, transient post-exposure prophylaxis (pep) of rabies infection, when given immediately after contact with a rabid or possibly rabid animal.,kamrab should be administered concurrently with a full course of rabies vaccine.,? do not administer additional (repeat) doses of kamrab once vaccine treatment has been initiated, since this may interfere with the immune response to the rabies vaccine.,? do not administer kamrab to patients with a history of a complete pre-exposure or post-exposure vaccination regimen and confirmed adequate rabies antibody titre.

Australia - English - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - rabies virus, quantity: 3.25 iu - diluent, not applicable - excipient ingredients: water for injections; sodium chloride - verorab is indicated for pre-exposure prophylaxis against rabies. verorab is indicated for post-exposure prophylaxis against rabies. verorab should be used in accordance with official local recommendations.