Vaccine Biovac (D + PAL) for dogs (1 dose) (2 ampoules vaccine + diluent 1 ml)

The price is for 1 dose

DESCRIPTION

The vaccine Biovac-DPAL is used against plague, infectious hepatitis, adenovirus, parvovirus enteritis and leptospirosis in dogs.

Dosage form: dry component - lyophilized mass; liquid component - suspension for injection (solvent for dry component).

Lyophilized component in appearance is a dry, porous mass of light beige, sometimes with a pale pink tint; the liquid component is a homogeneous suspension from pink to beige, which forms a loose sediment upon settling, which, when agitated, easily breaks up into a homogeneous suspension.

COMPOSITION

The dry component Biovac-D is made from a live attenuated strain of the plague carnivore virus EPMM with the addition of sorbitol and gelatose as a stabilizer at a final concentration of 5%.

Liquid component Biovac-PAL ml).

BIOLOGICAL PROPERTIES

The vaccine induces the formation of an immune response to the causative agents of plague, infectious hepatitis, adenovirosis, parvovirus enteritis and leptospirosis in puppies 2 weeks after a double administration, in adult animals 21 days after a single administration for 1 year. The vaccine is harmless and has no medicinal properties.

INDICATIONS

The vaccine is intended for the prevention of plague, infectious hepetitis, adenovirosis, parvovirus enteritis and leptospirosis in dogs.

APPLICATION

Before use, the contents of an ampoule or vial with a solvent are shaken, introduced into an ampoule or vial with a lyophilized component and mixed until a homogeneous suspension is formed. The vaccine is administered in compliance with the rules of septic and antiseptics; sterile syringes and needles are used for administration. The injection site is treated with 70% alcohol.

The vaccine is administered subcutaneously or intramuscularly according to the following scheme:

Puppies weighing up to 5 kg, twice, with an interval of 7-14 days Puppies weighing 5 kg or more, twice with an interval of 7-14 days Adult animals, once

1. Introduction 2 introduction 1. Introduction 2 introduction

1 dose of the dry component is dissolved in? doses of liquid component 1 dose of dry component is dissolved in 1 dose of liquid component 1 dose of dry component is dissolved in 1 dose of liquid component 1 dose of dry component is dissolved in 1 dose of liquid component 1 dose of dry component is dissolved in 1 dose of liquid component

Violations of the schedule (timing) of vaccine administration should be avoided, as this may lead to a decrease in the effectiveness of immunoprophylaxis. If the next vaccine injection is missed, it is necessary to immunize as soon as possible.

CONTRAINDICATIONS

It is forbidden to vaccinate clinically sick and / or weakened animals.

It is forbidden to use the vaccine together and within 14 days before and after the use of other immunobiological preparations, as well as within 10 days before and 14 days after deworming.

SPECIAL INSTRUCTIONS

Vaccine components in vials without labels, with an expired shelf life, in violation of the integrity and / or tightness of the package, with a changed appearance, with the presence of impurities, frozen, not used within 4 hours after opening, discarded, disinfected by boiling for 30 minutes and disposed of.

OVERDOSE

Symptoms of plague, parvovirus enteritis, hepatitis, adenovirosis, leptospirosis and other pathological signs in overdose have not been established.

SIDE EFFECTS

The peculiarities of the post-vaccination reaction during primary and subsequent immunizations have not been established.

When using the vaccine in accordance with this instruction, side effects and complications, as a rule, are not noted. In some animals, a swelling may develop at the vaccine injection site, which resolves within 3-5 days.

The timing of the possible use of products of animal origin after the introduction of the vaccine is not established.

PRECAUTIONS

When working with the vaccine, you should follow the general rules of personal hygiene and safety measures provided for when working with medicinal products for veterinary purposes. All persons involved in the vaccination must be dressed in protective clothing and provided with personal protective equipment. There must be a first aid kit at work places.

FIRST AID

If the vaccine comes into contact with the skin and / or mucous membranes, it is recommended to rinse them with plenty of running water. In case of accidental administration of the drug to a person, the injection site must be immediately treated with a 70% solution of ethyl alcohol, contact a medical institution.

STORAGE

The vaccine should be stored and transported in the manufacturer's closed packaging, in a dry, dark place at a temperature from + 2 В° C to + 10 В° C. The drug should be stored out of the reach of children. The shelf life under the storage conditions is 12 months from the date of manufacture, after the expiration date, the vaccine is not suitable for use.

PACKING

The dry component is packaged in 1 inoculation dose (0.5 cm?) In glass ampoules or vials of appropriate capacity; liquid component - 1 ml (1 dose) in glass ampoules or vials of appropriate capacity.

Specifications

KolVUP

five

Manufacturer

Biocenter

Temperature regime

from +2 to +8

Teaser

vaccine against plague, infectious hepatitis, adenovirosis, parvovirus enteritis and leptospirosis of dogs