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Newcastle-hepatitis
killed vaccine.
REG. SAGAR B-0258-054 CODE: 1112
DESCRIPTION
Inactivated oil emulsified vaccine against Newcastle Disease (ND) and inclusion
body hepatitis, hydropericardium syndrome or Angara disease (IBH) of chickens,
prepared from highly immunogenic strains of ND and IBH viruses. The vaccine contains
adjuvants in order to obtain high and long lasting immunity.
COMPOSITION
newcastle-hepatitis contains inactivated ND virus, La Sota strain and IBH adenovirus
group I of chicken embryo origin, emulsified in mineral oil.
INDICATIONS
Newcastle-hepatitis is recommended for vaccination and revaccination of healthy
birds 8 days or older as an aid for the prevention and control of ND and IBH.
Twenty four hours before vaccination warm the emulsion to room temperature (18-22ºC),
keeping the vaccine in dark out of refrigeration conditions. Shake well. During
application shake the vaccine every half hour.
DOSAGE
Vaccinate 0.5ml (1/2cc) to 1.0 ml (1cc) per bird.
ROUTE OF ADMINISTRATION
The vaccine should be administered subcutaneously in the midportion back of the
neck, between the head and the body, in direction away from the head.
No other method or route is suggested or implied.
PACKING
Plastic bottles with 500 ml.
STORAGE
Store in the dark, between 2-70C (35-45oF). Do not freeze.
The product can remain at room temperature (between 18ºC – 24ºC)
for no longer than 6 months without affecting its immunogenic properties. Avoid
direct exposure to solar rays.
CONTRAINDICATIONS
Vaccinate only healthy birds.
PRECAUTIONS
Use entire content when first opened. Do not store partially used containers of
vaccine for future use. Burn vaccine containers and unused content.
WARNING
It is imperative that the user of this product comply with the instructions stated
above.
The vaccine must be prepared and administered as directed to obtain best results.
Use of non-sterile needles, syringes and stoppers under field vaccinations may
result in abscess formation and condemnations of birds.
As it can happen with all emulsion vaccines, swelling and granulomas (usually
of small to moderate size) at site of injection can follow its application because
the oil adjuvants forms a repository of vaccine to provide prolonged antigenic
stimulation. This is non-inflamatory and will usually disappear within reasonable
period. This reactions can vary in severity by inappropiate vaccination technics
or when applied during molt. Swellings at site of injection
can be present for 2 or 3 weeks following administration.
Avoid injection into humans. If accidental injection occurs, seek medical attention
immediately since serious localized reaction may result.
ENGOREPROD 191-104 20080516
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