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Date: Saturday, May 18, 2024 10:33

Release 2.129
Neocolipor suspension for injection
 
Species: Pigs
Therapeutic indication: Immunological veterinary medical products: For pigs
Active ingredient: Vaccine Antigens
Product:Neocolipor Suspension for Injection
Product index: Neocolipor
Pig - meat: Zero days
Incorporating:
Qualitative and quantitative composition
Per dose of 2 ml:
Active substances:
E. coli adhesin F4 (F4ab, F4ac, F4ad), at least 2.1 SA.U*
E. coli adhesin F5, at least 1.7 SA.U*
E. coli adhesin F6, at least 1.4 SA.U*
E. coli adhesin F41, at least 1.7 SA.U*
*1 SA.U: quantity sufficient to obtain an agglutinating antibody titre of 1 log10 in the guinea pig.
Adjuvant: Aluminium (as hydroxide) 1.4 mg
Excipient: Thiomersal 0.2 mg
For the full list of excipients, see below.
Pharmaceutical form
Suspension for injection.
Clinical particulars
Target species
Pigs (sows and gilts).
Indications for use
Reduction of neonatal enterotoxicosis of piglets, caused by E. coli strains, expressing the adhesins F4ab, F4ac, F4ad, F5, F6 and F41, during the first days of life.
Contra-indications
None.
Special warnings for each target species
None.
Special precautions for use in animals
Since the protection of piglets in ensured by colostrum intake, each piglet should ingest a sufficient quantity of colostrum within 6 hours of birth. Vaccinate only healthy animals. Do not administer in conjunction with other products.
Special precautions to be taken by the person administering the product to animals
In the case of accidental self injection, seek medical advice immediately and show the package insert or label to a physician. Wash and disinfect hands after use.
Adverse reactions
Vaccination may cause slight hyperthermia (less than 1.5 °C during a maximum period of 24 hours).
Use during pregnancy, lactation or lay
No special precautions.
Interactions
No information is available on the compatibility of this vaccine with any other. Therefore the safety and efficacy of this product when used with any other (either when used on the same day or at different times) has not been demonstrated.
Amounts to be administered and administration route
Shake the vial vigorously before use. Use sterile syringe and needles. Administer using aseptic procedures.
One 2 ml dose intramuscularly in the neck in the area behind the ear, according the following schedule:
Primary vaccination
First injection: 5 to 7 weeks before farrowing
Second injection: 2 weeks before farrowing.
Revaccination:
1 injection 2 weeks before each subsequent farrowing.
Overdose
No undesirable effects have been observed after the administration of twice the recommended dosage.
Withdrawal period
Zero days.
The vaccine contains the inactivated strains of E. coli expressing the adhesins F4ab, F4ac, F4ad, F5, F6 and F41, which cause neonatal enterotoxicosis in piglets, in aluminium hydroxide adjuvant. In sows and gilts, the vaccine induces the specific seroconversion of vaccinated animals; piglets are passively immunised by intake of colostrum and milk containing adhesin-specific antibodies.
ATCvet code: QI09AB02
Pharmaceutical particulars
Excipients
Thiomersal, Aluminium hydroxide, Sodium chloride.
Major incompatibilities
Do not mix with any other vaccine.
Shelf life
Shelf life of the product as packaged for sale: 18 months at 2 – 8 °C.
Shelf life once the vial has been broached: 3 hours.
Special precautions for storage
Store and transport at 2 °C – 8 °C, protected from light. Do not freeze.
Immediate packaging
25 dose 50ml vial.
Disposal
Any unused product or waste materials derived from such products should be disposed of in accordance with local requirements.
Marketing Authorisation Holder (if different from distributor)
Boehringer Ingelheim Vetmedica GmbH
Binger Strasse 173
55216 Ingelheim am Rhein
Germany
Marketing Authorisation Number
UK(GB): Vm 04491/5026
UK(NI): EU/2/98/008/001-004
Significant changes
Legal category
Legal category: POM-V
GTIN
GTIN description:Neocolipor suspension for injection 50 ml
GTIN:3661103003915