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Trivacton 6 Immune Supplement

  • 50ml Bottle £50.57

Description

For administration to pregnant cows and heifers to stimulate serological and colostral antibodies against rotovirus and coronavirus antigens against K99, Y, 31A and F41 antigens of E.coli in susceptible animals which may be passed to the calf to reduce neonatal diarrhoea infection caused by agents containing these antigens.

Qualitative and quantitative composition

Each dose of 5 ml of vaccine contains:

E. coli K99 antigen, at least 1.15 SA.U

E. coli Y antigen, at least 0.9 SA.U

E. coli 31A antigen, at least 1.6 SA.U

E. coli F41 antigen, at least 0.7 SA.U

Inactivated bovine rotavirus, at least 3.0 SN.U

Inactivated bovine coronavirus, at least 1.9 SN.U

Aluminium hydroxide (expressed in Al+++) 3.5 mg

Saponin 1.5 mg

Thiomersal* 0.5 mg

Excipient q.s. 5 ml

1 SA.U: q.s. to obtain an agglutinating antibody titre of 1 log10 in mice after an administration of vaccine.

1 SN.U: q.s. to obtain a neutralizing antibody titre of 1 log10 in guinea pigs after two administrations of vaccine.

*Multidose containers only

For the full list of excipients, see below.

Pharmaceutical form

Suspension for injection.

Clinical particulars

Target species

Cattle (pregnant females).

Indications for use

For administration to pregnant cows and heifers to stimulate serological and colostral antibodies against rotavirus and coronavirus antigens and against K99, Y, 31A and F41 antigens of Escherischia coli in susceptible animals, which may be passed to the calf to reduce neonatal diarrhoea infection caused by agents containing these antigens.

Contra-indications

None.

Special warnings for each target species

None.

Special precautions for use

None.

Adverse reactions

Local reaction at the site of injection (≤10 cm), may appear after vaccination. This usually disappears within 14 days.

A slight increase in mean rectal temperature (≤0.5 °C) may be observed on the day following the injection.

Any injection of bacterial cells, even inactivated, may occasionally cause hypersensitivity reactions. In such cases, a symptomatic treatment should be provided.

Use during pregnancy, lactation or lay

For vaccination of pregnant cattle.

Interactions

No information is available on the safety and efficacy from the concurrent use 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 well before use. Subcutaneous route. Inject one 5 ml dose according to the following schedule:

Primary vaccination:

- First injection 1 to 2 months before calving.

-Second injection 2 to 4 weeks after first injection, at least 2 weeks prior to calving.

Boosters:

No data has been provided to support the use of a single dose booster regime. However, experience in the field suggests that a single dose of the vaccine administered two weeks before calving may provide enhanced antibody levels in the colostrum against the component antigens. Ensure that each calf rapidly ingests a sufficient quantity of colostrum.

Overdose

After administration of a double dose of vaccine, a local reaction at the site of injection may appear as a slight oedema evolving to a firm swelling, usually disappearing within 14 days of vaccination. A slight transient temperature rise (mean 0.7 °C) may be observed for two days following the injection.

Withdrawal periods

Zero days.

Pharmaceutical particulars

Excipients

Aluminium hydroxide, Saponin, Thiomersal.

Major incompatibilities

Do not mix with any other vaccine or immunological product.

Shelf life

Shelf life of the product as packaged for sale: 18 months. Open bottle should be used immediately.

Special precautions for storage

Store between +2 °C and +8 °C, protected from light.

Immediate packaging

10 dose (50 ml) bottle.

Disposal

Any unused product or waste materials derived from such products should be disposed of in accordance with local requirements.

Marketing authorisation number

Vm 08327/4106.

Legal category

POM-VPS

GTIN (Global Trade Item No)

Trivacton 6 10 dose bottle

03661103005339

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