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Date: Saturday, June 21, 2025 19:42

Release 2.33
Poulvac IB H120 lyophilisate for suspension for oculonasal use, ocular use or use in drinking water for chickens (NI)
 
Species: Chickens
Therapeutic indication: Immunological veterinary medical products: For poultry
Active ingredient: Vaccine Antigens
Product:Poulvac® IB H120
Product index: Poulvac IB H120
Poultry - meat: Zero days
Poultry - eggs: Zero days
Incorporating:
Qualitative and quantitative composition
Each dose contains:
Active substance:
Live attenuated avian infectious bronchitis virus, strain H120:
103.0 – 104.9 EID50*.
*EID50 = 50% embryo infective dose.
Excipients:
Qualitative composition of excipients and other constituents
D-mannitol
Gelatine
Myo-Inositol
Casein enzymatic hydrolysate
Off-white to cream coloured lyophilisate.
Pharmaceutical form
Please refer to the "Qualitative and quantitative composition" section.
Clinical particulars
Target species
Chickens.
Indications for use for each target species
For the active immunisation of chickens (broilers, future layers or breeders) in order to reduce the detrimental effect on the ciliary activity resulting from infection with infectious bronchitis virus (IBV) Massachusetts serotype strains, which is related to the development of respiratory clinical signs.
Onset of immunity: 25 days after vaccination.
Duration of immunity: 16 weeks.
Contraindications
None.
Special warnings
Vaccinate healthy animals only.
Maternally derived antibodies (MDA) can interfere with the development of active immunity. Where it is likely that recent field infection or vaccination of the parent flock has stimulated a high antibody titre and consequently a high level of MDA, the timing of the vaccination programme should be planned accordingly.
Special precautions for use
Special precautions for safe use in the target species:
The vaccine strain can spread to unvaccinated chickens. Special precautions should be taken to avoid spreading of the vaccine strain to unvaccinated chickens. It is recommended to vaccinate all birds on a site at the same time.
Special precautions to be taken by the person administering the veterinary medicinal product to animals:
Personal protective equipment consisting of goggles and dust masks or a helmet with filtered air circulation should be worn when handling the veterinary medicinal product especially while vaccination according to the spraying method.
Personnel involved in attending vaccinated chickens should follow general hygiene principles (changing clothes, wearing gloves, cleaning and disinfection of boots).
Special precautions for the protection of the environment:
Not applicable.
Adverse events
Chickens:
Very rare
(<1 animal / 10,000 animals treated, including isolated reports):
Respiratory signs1
1Generally mild and transient in nature.
Reporting adverse events is important. It allows continuous safety monitoring of a veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to either the marketing authorisation holder or the national competent authority via the national reporting system. See the package leaflet for respective contact details.
Use during pregnancy, lactation or lay
The safety of the veterinary medicinal product has not been established during lay.
Do not use in birds in lay and within 4 weeks before the start of the laying period.
Interaction with other medicinal products and other forms of interaction
No information is available on the safety and efficacy of this vaccine when used with any other veterinary medicinal product. A decision to use this vaccine before or after any other veterinary medicinal product therefore needs to be made on a case by case basis.
Administration routes and dosage
Vaccination scheme:
For chickens from one day of age.
One dose per chicken to be administered by coarse spray, by eye drop or with drinking water. The quantity of water to be used depends on the method of administration. Never use less than 1 dose per chicken.
For spray administration (oculonasal use):
The product can be used in most types of spray equipment. The equipment should provide coarse spray (droplets between 80 to 160 μm). The distance from the spraying head to the bird must be approximately 50 cm. Dilute and administer the reconstituted vaccine at a rate of one dose of reconstituted vaccine per bird, according to the directions of your specific coarse spray vaccination equipment. It is recommended to use 0.15 to 0.5 litres of water per 1,000 birds depending of the type of spray equipment to be used.
During spraying and for about 20 – 30 minutes thereafter, ventilation should be switched off or reduced. Dimming light sources is recommended to avoid unsettling the animals.
For eye drop administration (ocular use):
Use 30 to 50 ml of deionized water per 1,000 doses (birds) depending on the type of eye-dropper to be used. One drop equal to one dose (0.03 to 0.05 ml depending on the reconstituted volume) of the vaccine solution is administered into one eye per chicken. The deionised water should be at room temperature when used. Hold the chicken so that one eye is pointing upwards and allow one drop of vaccine to fall into the eye. Chickens should swallow during vaccination.
For drinking water administration (use in drinking water):
Discontinue any drinking water medication 24 hours before vaccination. Water containing a high level of free chlorine should not be used. A general indication is that if chlorine can be detected in the water by smell or taste it could deactivate the living virus. If so, half a litre of skimmed milk should be thoroughly mixed into every 20 litres of water or skimmed milk powder added at a rate of two grams per litre of water before adding vaccine.
Only perfectly clean and rust-free utensils and drinkers (preferably plastic) free of any trace of disinfectants, detergents, soap, etc. should be used. Ensure that there is enough drinking trough space to allow all chickens immediate access to the vaccine. No untreated water should be made available until the treated water has been consumed.
Withhold drinking water for 2 hours before vaccination to stimulate thirst. Remove the aluminium seal from the vaccine vial. To dissolve the vaccine pellet, the rubber stopper should then be removed whilst the vial is immersed in a plastic measuring jug containing 1 litre (approximately 1 quart) of clean cool water. Half fill the vial with water, replace the stopper and shake to dissolve any remaining vaccine.
The vaccine concentrate should then be added to and thoroughly mixed with sufficient drinking water to last for approximately 2 hours.
The approximate drinking water requirements for vaccination can be calculated from the age of the chickens. Use as many litres of water as the age of the chickens in days, per 1,000 chickens, up to a maximum of 40 litres per 1,000 chickens.
Distribute the diluted vaccine evenly in the drinkers. Do not expose prepared drinking water vaccine to sunlight.
The vaccine suspension is best divided so that the drinkers are charged at least twice with vaccine to ensure a more widespread uptake.
If nipple drinkers are employed, ensure that header tanks are continually refilled with water containing vaccine.
The vaccine may be used in automatic watering equipment. However, the main supply should only be turned on when all the vaccine treated water has been consumed. Return to regular watering only after the vaccine water has been consumed.
Upon reconstitution, transparent to white opaque suspension (depending on the volume of diluent used).
Symptoms of overdose (and where applicable, emergency procedures and antidotes)
Administration of a 10-fold overdose does not result in symptoms different from those mentioned under section "Adverse events".
Special restrictions for use and special conditions for use, including restrictions on the use of antimicrobial and antiparasitic veterinary medicinal products in order to limit the risk of development of resistance
Not applicable.
Withdrawal periods
Zero days.
Pharmacological particulars
Immunological information
ATCvet code: QI01AD07
This vaccine is intended to stimulate active immunity against Massachusetts strains of infectious bronchitis virus (IBV).
Pharmaceutical particulars
Major incompatibilities
Do not mix with any other veterinary medicinal product.
Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 2 years.
Shelf life after reconstitution according to directions: 4 hours.
Special precautions for storage
Store and transport refrigerated (2 °C – 8 °C).
Protect from light.
Do not freeze.
Nature and composition of immediate packaging
Glass vials closed with butyl rubber stopper and sealed with an aluminium crimp cap.
Pack sizes:
Cardboard box of 1 x 1,000 doses
Cardboard box of 1 x 2,500 doses
Cardboard box of 1 x 5,000 doses
Cardboard box of 1 x 10,000 doses
Cardboard box of 10 x 1,000 doses
Cardboard box of 10 x 2,500 doses
Cardboard box of 10 x 5,000 doses
Cardboard box of 10 x 10,000 doses
Not all pack sizes may be marketed.
Special precautions for the disposal of unused veterinary medicinal products or waste materials derived from the use of such products
Medicines should not be disposed of via wastewater or household waste.
Use take-back schemes for the disposal of any unused veterinary medicinal product or waste materials derived thereof in accordance with local requirements and with any national collection systems applicable to the veterinary medicinal product concerned.
Marketing Authorisation Holder (if different from distributor)
Zoetis Belgium S.A.
Marketing Authorisation Number
Vm 60021/3068
Significant changes
Date of the first authorisation or date of renewal
17 October 2005
Date of revision of the text
April 2025
Any other information
Classification of veterinary medicinal products
Veterinary medicinal product subject to prescription.
Detailed information on this veterinary medicinal product is available in the Union Product Database (https://medicines.health.europa.eu/veterinary).
Legal category
Legal category: POM-V
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