Vivitonin 100 mg Tablets for Dogs

Composition

Each tablet contains:

Active substance:

Propentofylline 100 mg

Excipients:

Ochre, biconvex and oblong film-coated tablets with a breaking line on one side and “K100” debossed on both sides of the breaking line.

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Pharmacological properties

4.1 ATCvet code: QC04AD90.

4.2 Pharmacodynamics

Propentofylline has been shown to increase blood flow, particularly of the heart and skeletal muscle. It also increases the blood flow of the brain and therefore its oxygen supply, without increasing the brain's glucose demand. It has a modest positive chronotropic effect and a marked positive inotropic effect. In addition, it has been shown to have an antiarrhythmic effect in dogs with myocardial ischemia and a bronchodilator action equivalent to that of aminofylline.

Propentofylline inhibits platelet aggregation and improves the flow properties of erythrocytes.

It has a direct effect on the heart and reduces peripheral vascular resistance thereby lowering cardiac load.

4.3 Pharmacokinetics

After oral administration, propentofylline is rapidly and completely absorbed and quickly distributed into the tissues. Maximum plasma levels are reached by 15 minutes following oral dosing in dogs.

The half-life is approximately 30 minutes and the bioavailability of the parent compound is approximately 30%.

There are a number of effective metabolites and biotransformation takes place mainly in the liver.

80-90% of propentofylline is excreted in the form of metabolites via the kidneys. The rest is eliminated with the faeces.

There is no bioaccumulation.

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Target species

Dogs.

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Indications

For improvement in dullness, lethargy and overall demeanour in dogs. The veterinary medicinal product is particularly useful in older dogs, where it may increase willingness to exercise and exercise tolerance.

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Dosage

Oral use.

Half a tablet per 10 kg body weight twice a day.

The 100 mg tablets should not be quartered.

More accurate dosing may be achieved using a combination of Vivitonin 100 mg and Vivitonin 50 mg tablets. Dogs of less than 20 kg can be given Vivitonin 50 mg tablets.

The tablets can be administered directly onto the back of the dog's tongue or can be mixed in a small ball of food and should be administered at least 30 minutes before feeding.

Divide the tablets in halves with a knife or with a tablet splitter.

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Contraindications

Do not administer to pregnant bitches or breeding animals.

Do not use in cases of hypersensitivity to the active substance or to any of the excipients.

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Adverse reactions

Dogs:

1 Particularly at the commencement of therapy.

2 Necessitates discontinuation of treatment.

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 its local representative or the national competent authority via the national reporting system. See the package leaflet for respective contact details.

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Warnings

Special precautions for safe use in the target species:

Specific diseases (e.g. kidney disease) should be treated accordingly.

In the case of renal failure, the dose should be reduced.

Consideration should be given to rationalising the medication of dogs already receiving treatment for congestive heart failure or bronchial disease.

Special precautions to be taken by the person administering the veterinary medicinal product to animals:

Care should be taken to avoid accidental ingestion.

Wash hands after use.

Special precautions for the protection of the environment:

Not applicable.

3.11 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.

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Use during pregnancy, lactation or lay

Pregnancy:

Do not use in pregnant bitches. The safety of the veterinary medicinal product has not been established during pregnancy.

Fertility:

Do not use in breeding animals.

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Interactions

None known.

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Overdose

Symptoms of cardiac and cerebral overstimulation have been observed. In such cases, animals should be treated symptomatically.

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Special warnings

None.

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Withdrawal period

Not applicable.

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Incompatibilities

None known.

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Immediate packaging

Polyvinyl chloride/aluminium foil blister packs of 6 x 10 tablets.

Pack size:

Cardboard box containing 60 tablets, presented in 6 blister strips of 10 tablets.

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Storage

Do not store above 25 °C.

Store in a dry place.

Return any half tablets to the original packaging.

Keep the blister packs in the outer carton.

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Shelf life

Shelf life of the veterinary medicinal product as packaged for sale: 3 years.

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Disposal of unused product

Medicines should not be disposed of via wastewater.

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.

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Additional information

Vm 06376/4078

8 DATE OF FIRST AUTHORISATION

30 September 1994

9 DATE OF THE LAST REVISION OF THE SUMMARY OF THE PRODUCT CHARACTERISTICS

October 2025

10 CLASSIFICATION OF VETERINARY MEDICINAL PRODUCT

Veterinary medicinal product subject to prescription.

Find more product information by searching for the ‘Product Information Database’ on www.gov.uk.

Approved: 15 October 2025

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Registration holder

Intervet International B.V.

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