Online Pet Medications & Pet Supplies

ZODON TABS 88MG X 120

Category: Z

Select Option
ZODON TABS 88MG X 120 - £ 84.40
QTY:
Product REF: CEZOD02
ZODON TABS 264MG X 120 - £ 159.60
QTY:
Product REF: CEZOD04

Total Price: £0.00


Vat Rate: 20%

Prescription Required



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.

Our Standard Delivery - £6.75

Royal Mail Tracked 24 (Signed For)

  • Next business day service
  • Compensation cover up to £100
  • Signature on delivery

 

Any orders placed after close of business on Thursday will not be delivered until Tuesday

 

 

 

Our Express Delivery - £10.45

Royal Mail Special Delivery Guaranteed by 1pm

  • Next business day service
  • Insured up to £500
  • Signature on delivery

 

Please note that all chilled deliveries must be sent on an Express service.

Chilled orders placed after close of business on Wednesday will not be despatched until Monday

You must be logged in to write review
Category POM-V
Temperature Ambient
MA/VM/EU No: 15052/4128
Species
  • dogs
VMD Link https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_618387.PDF
NOAH Link
Dosage Amounts to be administered and administration route For oral administration. For the treatment of infected wounds and abscesses, and oral cavity/dental infections including periodontal disease, administer either: -5.5 mg/kg of bodyweight every 12 hours for 7-10 days, or -11 mg/kg of bodyweight every 24 hours for 7-10 days If no clinical response is seen within 4 days, redetermine the diagnosis. For the treatment of superficial pyoderma in dogs, administer either: -5.5 mg/kg of bodyweight every 12 hours, or -11 mg/kg of bodyweight every 24 hours Therapy of superficial pyoderma is usually recommended for 21 days, with extension of therapy based on clinical judgement. 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 example: For a dose regimen of 11mg/kg Weight (kg) Zodon 88 mg No. tablets per administration Weight (kg) Zodon 264 mg No. tablets per administration 1.0-2.0 1/4 4.5-6.0 1/4 2.1-4.0 1/2 6.1-9.0 Use Zodon 88 mg 4.1-6.0 3/4 9.1-12.0 1/2 6.1-8.0 1 12.1-18.0 3/4 8.1-10.0 1
Withdrawals