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Date: Tuesday, May 20, 2025 17:03

Release 2.25
Rispoval RS+PI3 IntraNasal nasal spray, lyophilisate and solvent for suspension for cattle (NI)
 
Species: Cattle
Therapeutic indication: Immunological veterinary medical products: For cattle
Product:Rispoval® RS+P13 Intranasal
Product index: Rispoval RS+PI3 Intranasal
Cattle - milk: Zero days
Cattle - meat: Zero days
Incorporating:
Qualitative and quantitative composition
Each 2 ml dose contains:
Active substances:
Lyophilisate
Bovine parainfluenza virus 3 (PI3V), strain RLB 103, live
105.0 - 108.6 CCID50.
Bovine respiratory syncytial virus (BRSV), strain 375, live
105.0 - 107.2 CCID50.
CCID50: Cell Culture Infective Dose 50%.
Excipients:
Qualitative composition of excipients and other constituents
Lyophilisate:
Buffered lactose solution
Gelatin solution
Casein hydrolysate solution
HALS medium
Solvent:
Sodium chloride
Water for injections
Lyophilisate: slightly whitish to yellowish freeze-dried pellet.
Solvent: clear colourless liquid, free from visible impurities.
Pharmaceutical form
Please refer to the "Qualitative and quantitative composition" section.
Clinical particulars
Target species
Cattle.
Indications for use for each target species
For vaccination with Rispoval RS+PI3 IntraNasal only:
For active immunisation of maternally derived antibody positive or negative calves from 9 days of age against BRSV and PI3V, to reduce the mean titre and duration of excretion of both viruses.
Onset of immunity: 5 days for BRSV and 10 days for PI3V after a single vaccination.
Duration of immunity: 12 weeks after a single vaccination. The duration of protective immunity against the PI3V fraction may be reduced in MDA positive calves vaccinated before 3 weeks of age.
For primary vaccination using Rispoval RS/Pi3 IntraNasal and booster vaccination with Rispoval 2/BRSV + Pi3*, refer to the Rispoval 2/BRSV Pi3* product information for specific details on indications.
* Where this veterinary medicinal product is authorised.
Contraindications
None.
Special warnings
Vaccinate healthy animals only.
Animals should preferably be vaccinated at least 10 days before a period of stress or high infection risk like re-grouping or transport of animals, or at the start of the autumn season. To achieve optimal results, it is recommended to vaccinate all the calves within the same herd.
Special precautions for use
Special precautions for safe use in the target species:
Vaccinal viruses can spread from vaccinated to non-vaccinated calves and may cause a serological response, but without causing clinical signs. In laboratory experiments based on the data using 3 week-old animals, shedding was observed for BRSV and PI3V up to 11 and 7 days respectively after vaccination with one dose containing the maximal virus content.
Special precautions to be taken by the person administering the veterinary medicinal product to animals:
Not applicable.
Special precautions for the protection of the environment:
Not applicable.
Adverse events
Cattle:
Rare
(1 to 10 animals / 10,000 animals treated):
Hypersensitivity reaction(e.g. anaphylactic-type reaction)
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
Pregnancy and lactation:
The safety and efficacy of the veterinary medicinal product has not been established during pregnancy and lactation. Do not use during pregnancy and lactation.
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
Dose: 2 ml.
Route: nasal use.
Reconstitution of the vaccine:
Reconstitute the 1 dose and 5 dose presentations by aseptically adding the solvent to the vial containing the lyophilisate. Shake well before use.
Reconstitute the 25 dose presentation by mixing the lyophilised fraction with the solvent in 2 steps:
1. Inject 10 ml of the solvent on the lyophilised plug in the vial containing the lyophilisate.
2. Shake well and extract the reconstituted lyophilised fraction from the vial and mix with the remaining solvent in the liquid fraction vial.
Shake well before use.
Reconstituted product: pink to orange liquid, which might contain a loose resuspendable sediment.
Vaccination programme:
Basic vaccination: A single dose of 2 ml of reconstituted vaccine should be given using the intranasal applicator available from Zoetis to cattle from the age of 9 days.
It is recommended to change applicators between animals to avoid transmitting infectious organisms.
For primary vaccination using Rispoval RS/Pi3 IntraNasal and booster vaccination with Rispoval 2/BRSV + Pi3*, refer to the Rispoval 2/BRSV Pi3* product information for specific details on vaccination programme.
* Where this veterinary medicinal product is authorised.
Symptoms of overdose (and where applicable, emergency procedures and antidotes)
In colostrum-deprived animals vaccinated before 3 weeks of age with a 10-fold overdose of vaccine, transient temperature increase, nutritional scour, abnormal faeces and demeanour were observed.
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: QI02AD07
To stimulate active immunity against BRSV and PI3V.
Pharmaceutical particulars
Major incompatibilities
Do not mix with any other veterinary medicinal product, except solvent supplied for use with the veterinary medicinal product.
Shelf life
Shelf life of the veterinary medicinal product as packaged for sale (5 and 25 doses presentations): 2 years.
Shelf life of the veterinary medicinal product as packaged for sale (1 dose presentation): 1 year.
Shelf life after reconstitution according to directions: 2 hours.
Special precautions for storage
Store and transport refrigerated (2 °C - 8 °C).
Do not freeze.
Protect from light.
Nature and composition of immediate packaging
Cardboard box with 1 glass vial of 5 or 25 doses of lyophilisate accompanied by 1 glass vial containing respectively 10 or 50 ml of solvent. Both vials have rubber stopper and aluminium cap.
Plastic box with 5 glass vial(s) of 1 dose of lyophilisate accompanied by 5 glass vial(s) containing 2 ml of solvent. Both vials have rubber stopper and aluminium cap.
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 UK Limited
1st Floor, Birchwood Building
Springfield Drive
Leatherhead
Surrey
KT22 7LP
Marketing Authorisation Number
Vm 42058/3038
Significant changes
Date of the first authorisation or date of renewal
11 October 2005
Date of revision of the text
September 2024
Any other information
Classification of veterinary medicinal products
Veterinary medicinal product subject to prescription.
Find more product information by searching for the ‘Product Information Database’ or ‘PID’ on www.gov.uk.
Legal category
Legal category: POM-V
GTIN
GTIN description:1 dose:
GTIN:05414736028156
GTIN description:5 dose:
GTIN:05013457079562
GTIN description:25 dose:
GTIN:05013457079838