Category: R
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| Category | POM-V |
| Temperature | Refrigerated |
| MA/VM/EU No: | 42058/4127 |
| Species |
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| VMD Link | https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_163149.PDF |
| NOAH Link | |
| Dosage | Dose Cattle over 3 months of age: 2 ml. Route Subcutaneous injection. Shake the vaccine well before use. Vaccination Scheme The vaccination scheme consists of basic immunisation and booster vaccinations. Basic Immunisation Two doses, each of 2 ml, 3-5 weeks apart. Booster vaccinations of cattle having been administered the primary vaccination scheme using Rispoval IBR Marker Inactivated One dose of 2 ml at 6 monthly intervals. Booster vaccinations of cattle having been administered the primary vaccination scheme using Rispoval IBR Marker Live Cattle having been administered the primary vaccination scheme using Rispoval IBR-Marker Live (according to the product information for this product) may be given booster vaccinations with Rispoval IBR-Marker Inactivated. These animals should be given a single dose booster vaccination with Rispoval IBR-Marker Inactivated 6 months after their initial vaccination course with Rispoval IBR-Marker Live. Thereafter, single dose booster vaccinations with Rispoval IBR-Marker Inactivated should be administered every 12 months. It is recommended that all cattle in the herd are vaccinated. Use only sterile needles and syringes for administration. Avoid the introduction of contamination during use. Due to the presence of maternal antibodies, the development of immunity in calves under 3 months of age may be impaired. These animals should be re-vaccinated when they are over 3 months of age. To prevent abortions associated with BoHV-1, female cattle require a primary course of two subcutaneous doses of vaccine 3-5 weeks apart or alternatively a primary course of a single intramuscular dose of Rispoval IBR-Marker Live followed 6 months later by a single dose booster using Rispoval IBR-Marker Inactivated. In order to cover the main abortion risk period, it is recommended that the second dose of the primary course of two subcutaneous doses or the single dose booster using Rispoval IBR-Marker Inactivated is administered no later than by the start of the second trimester of each pregnancy. Method of administration Shake the vaccine well before use. The liquid suspension is injected aseptically via the subcutaneous route. Vaccination schemes summary From 2 weeks to 3 months of age Rispoval IBR-Marker Vaccine Used Primary vaccination Revaccination Intervals First dose, from 2 weeks of age (route of administration) Second dose at 3 months of age (route of administration) Interval to next booster vaccination (vaccine and route of administration) All subsequent booster vaccinations (vaccine and route of administration) Live (IN) Live (IM) 6 Months (Live IM) 6 Months (Live IM) Live (IN) Live (IM) 6 Months (Inactivated SQ) 12 months (Inactivated SQ) From 3 months of age Rispoval IBR-Marker Vaccine Used Revaccination Intervals Primary vaccination (number of doses and route of administration) Interval to first booster vaccination (vaccine and route of administration) All subsequent booster vaccinations (vaccine and route of administration) Live (one dose IM) 6 Months (Live IM) 6 Months (Live IM) Live (one dose IM) 6 Months (Inactivated SQ) 12 Months (Inactivated SQ) Inactivated (two doses with 3 - 5 Week Interval SQ) 6 Months (Inactivated SQ) 6 Months (Inactivated SQ) For female cattle for protection against abortion Rispoval IBR-Marker Vaccine Used Revaccination recommended to be applied no later than by the start of the second trimester of each pregnancy Vaccine schedule (number of doses and route of administration) recommended to be applied no later than by the start of the second trimester of pregnancy Live (two doses with 3-5 week interval IM) Inactivated (one dose SQ) Live (one dose IM) followed by Inactivated (on edose SQ) with 6 months interval Inactivated (one dose SQ) Inactivated (two doses with 3-5 week interval SQ) Inactivated (one dose SQ) For vaccination in known high BoHV-1 infection pressure Rispoval IBR-Marker Vaccine Used Revaccination Intervals Primary vaccination (number of doses and route of administration) Interval to first booster vaccination (vaccine and route of administration) All subsequent booster vaccinations (vaccine and route of administration) Live (one dose IN) followed by Live (one dose IM) with 3-5 weeks interval 6 Months (Live IM, OR Inactivated SQ) 6 Months (Live IM) OR 12 months (Inactivated SQ) |
| Withdrawals | Do not use in unhealthy animals. Transient subcutaneous swelling up to 5 cm in diameter, which subsides within 14 days, may occur at the injection site in very rare cases. In very rare cases allergic reactions may occur as with other vaccines, therefore vaccinates should be observed for approximately 30 minutes following immunisation. In those cases, anti-allergics should be administered. Immunosuppressive substances e.g. corticosteroids or Bovine Viral Diarrhoea modified live vaccines, should be avoided for a period of 7 days prior to and after vaccination as this may impair the development of immunity. Can be used during pregnancy and lactation. 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 decided on a case by case basis. Do not mix with any other veterinary medicinal product. Withdrawal periods Zero days. User warnings In case of accidental self-injection, seek medical advice immediately and show the package leaflet or the label to the physician. |
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