Zodon chewable tablets for dogs are an effective oral medication for the treatment of infected wounds, abscesses and oral cavity infections, including periodontal disease, caused by Staphylococcus spp. (except Streptococcus faecalis), bacteroides spp., fusobacterium necrophorum and Clostridium perfringens.

Zodon is also highly effective in treating dogs with superficial pyoderma associated with staphylococcus pseudintermedius and osteomyelitis caused by Staphylococcus aureus. The active ingredient in Zodon is Clindamycin antibiotic.

We sell Zodon tablets in packs of 120 tablets. They are shaped like a clover, beige in colour and scored in four parts so they can be broken up easily. It is recommended to store Zodon at an ambient room temperature.

How To Buy Zodon Chewable Tablets

Zodon chewable dog tablets are a prescription-only medication. This means that before you complete your purchase, you are required to upload a prescription through our online portal.

After our team has confirmed you've ordered the right medication for your dog, we can send out your order. It's a simple process that means you can buy Zodon dog medication online instead of going to your vet every month.

How To Use Zodon Chewable Tablets

Zodon dog tablets are for oral administration only and the flavoured tablets are easy for your dog to swallow and digest.

Used for the treatment of infected wounds, abscesses and oral cavity infections, the following average doses are advised. However, the actual dose used should be determined by the severity of the signs and the length of time for which they have been present.

5.5mg per 1kg of body weight every 12 hours for 7-10 days or 11mg per 1kg of bodyweight every 24 hours for 7-10 days if no clinical response is seen within 4 days. For the treatment of superficial pyoderma in dogs: 5.5 mg/kg of bodyweight every 12 hours or 11 mg per 1kg of bodyweight every 24 hours. Therapy of superficial pyoderma is recommended for 21 days, with an extension on this based on clinical judgement by a veterinarian.

For the treatment of osteomyelitis in dogs, administer 11 mg/kg of bodyweight every 12 hours for a minimum of 28 days. If no clinical response is seen within 14 days, the treatment should be stopped and the diagnosis redetermined.

For more information on Zodon chewable tablets for dogs and how to use them, please see the product label or contact your veterinarian.

Special Precautions

The active ingredient Clindamycin should not be given to hamsters, guinea pigs, rabbits or horses because this can cause severe digestive problems.

You should wash your hands after administering Zodon. People with known hypersensitivity to lincosamides (lincomycin and clindamycin) should avoid handling Zodon.

Adverse reactions observed when taking Zodon include vomiting and diarrhoea.

Target species

Dogs

Indications for use, specifying the target species

• For the treatment of infected wounds and abscesses, and oral cavity infections including periodontal disease, caused by or associated with Staphylococcus spp., Streptococcus spp. (except Streptococcus faecalis), Bacteroides spp., Fusobacterium necrophorum, and Clostridium perfringens.
• For the treatment of superficial pyoderma associated with Staphylococcus pseudintermedius.
• For the treatment of osteomyelitis, caused by Staphylococcus aureus.

Contraindications

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

Do not administer to rabbits, hamsters, guinea pigs, chinchillas, horses or ruminants because ingestion of clindamycin by these species may result in severe gastro-intestinal disturbance.

Special warnings for each target species

None.

Special precautions for use

Special precautions for use in animals

The chewable tablets are flavoured. In order to avoid any accidental ingestion, store tablets out of reach of the animals. Use of the product should be based on susceptibility testing of the bacteria isolated from the animal. Official and local antimicrobial policies should be taken into account when the product is used. Use of the product deviating from the instructions given in the SPC may increase the prevalence of bacteria resistant to clindamycin and may decrease the effectiveness of treatment with lincomycin or macrolide antimicrobials due to the potential for cross resistance.

Clindamycin and erythromycin show parallel resistance. Partial cross-resistance has been demonstrated between clindamycin, erythromycin and other macrolide antibiotics. During prolonged therapy of one month or greater, periodic liver and kidney function tests and blood counts should be performed. Animals with severe renal and/or very severe hepatic disturbances accompanied by severe metabolic aberrations should be dosed with caution and should be monitored by serum examination during high-dose clindamycin therapy. Special precautions to be taken by the person administering the veterinary medicinal product to animals

People with known hypersensitivity to lincosamides (lincomycin and clindamycin) should avoid contact with the veterinary medicinal product. Wash hands after handling tablets. Accidental ingestion may result in gastro-intestinal effects such as abdominal pain and diarrhoea. Care should be taken to avoid accidental ingestion. In case of accidental ingestion, particularly by children, seek medical advice immediately and show the package leaflet or the label to the physician.

Adverse reactions (frequency and seriousness)

Vomiting and diarrhoea have been reported very rarely. Hypersensitivity reactions and thrombocytopenia have been reported very rarely. Clindamycin sometimes causes the overgrowth of non-sensitive organisms such as clostridia and yeasts. In cases of superinfection, appropriate measures must be taken according to the clinical situation.

Use during pregnancy, lactation or lay

While high dose studies in rats suggest that clindamycin is not a teratogen and does not significantly affect the breeding performance of males and females, safety in gestating bitches or breeding male dogs has not been established. Clindamycin crosses the placental and the blood-milk barrier. Treatment of lactating females can cause diarrhoea in puppies. Use the product only according to the benefit/risk assessment by the responsible veterinarian. The use of the product is not recommended in neonates.

Interaction with other medicinal products and other forms of interaction

Clindamycin hydrochloride has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. The product should be used with caution in animals receiving such agents.

Clindamycin should not be combined with erythromycin or other macrolides to prevent macrolide-induced resistance to clindamycin.

Clindamycin may reduce plasma levels of cyclosporin with a risk of lack of activity.

During the simultaneous use of clindamycin and aminoglycosides (eg gentamicin), the risk of adverse interactions (acute renal failure) cannot be excluded.