Pardale-V is a non-prescription analgesic and anti-inflammatory medication for use in dogs. It is suitable for use after injuries or in other painful conditions. It is often used to help joint pain. It is not recommended to be given continuously; a 5 day course should be all that is needed, though repeat courses can be given after a suitable break. If in doubt, consult your veterinary surgeon. (NFA-VPS)
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Pardale-V Tablets for Dogs » Pack of 100Estimated dispatch within 24 working hours. TVP: £33.24 Our price: £18.60 Buy
Pardale-V Tablets for Dogs » Pack of 500Out of stock since Thu 12th Dec 2013, due back soon. TVP: £152.47 Our price: £82.47 Buy
Below is the product datasheet. This has been provided by the manufacturer and should always be provided with the medication.
Company name: Dechra Veterinary Products Limited
Address: (A business unit of Dechra Pharmaceuticals PLC)
Sansaw Business Park
Shropshire SY4 4AS
Telephone: 01939 211200
Fax: 01939 211201
White, flat tablets with a bevelled edge and a break-line.
Each tablet contains:
Active substances: Paracetamol 400 mg
Codeine phosphate hemihydrate 9 mg
For analgesic therapy in the dog only. The product is indicated for acute pain of traumatic origin, as a complementary treatment in pain associated with other conditions, and post operative analgesia.
Dosage and administration
For oral administration.
1 tablet per 12 kg body weight every 8 hours.
Small dogs (up to 6 kg body weight): Half a tablet every 8 hours.
Medium dogs (6-18 kg body weight): Half to one and a half tablets every 8 hours.
Large dogs (18-42 kg body weight): 1-3 tablets every 8 hours.
Treat for a maximum of 5 days.
Contraindications, warnings, etc
Do not exceed the stated dose or the duration of treatment.
Do not administer other NSAIDs concurrently or within 24 hours of each other.
Use is contraindicated in animals suffering from cardiac, hepatic or renal disease, where there is the possibility of gastrointestinal ulceration or bleeding, or where there is evidence of blood dyscrasia or hypersensitivity to the product.
Do not use this preparation for cats.
Use in animals less than 6 weeks of age, or in aged animals, may involve additional risk. If such use cannot be avoided, animals may require a reduced dosage and careful clinical management.
Avoid use in dehydrated, hypovolaemic or hypotensive animals as there is a potential risk of increased renal toxicity.
Some NSAIDS may be highly bound to plasma proteins and compete with other highly bound drugs to produce an increase in non-bound pharmacologically active concentrations, which can lead to toxic effects.
Concurrent administration of potentially nephrotoxic drugs should be avoided.
There are no known contraindications for use during pregnancy.
If you notice any serious effects or other effects not mentioned in the data sheet, please inform your veterinary surgeon.
Overdose: Immediately seek the advice of a veterinary surgeon showing them the product literature.
Carry out lavage and treat with an intravenous injection of acetylcysteine (200 mg/ml) at a rate of 140 mg/kg every 6 hours for 7 treatments. Ascorbic acid (30 mg/kg) should also be given orally with each dose of acetylcysteine. If necessary, instigate fluid therapy using 'Ringers' or bicarbonate solution. Treat for codeine overdosing with intravenous injections of naloxone (1.0 mg/kg) repeated as necessary. Provide oxygen support.
Side effects: Occasional constipation due to codeine content.
Special precautions to be taken by the person administering the veterinary medicinal product to animals: Wash hands after use.
General precautions: For animal treatment only.
Keep out of the reach and sight of children.
Do not store above 25C.
Do not use after the expiry date stated on the blister.
Disposal: Dispose of empty packaging and any remaining product in the household refuse.
Containers of 100 and 500 tablets.
NSAIDs can cause inhibition of phagocytosis and hence in the treatment of inflammatory conditions associated with bacterial infections, appropriate concurrent antimicrobial therapy should be instigated.
Seek veterinary advice if the treated condition does not improve or worsens during treatment.
UK authorised veterinary medicinal product.
Marketing authorisation holder (if different from distributor)
Dechra Limited, Dechra House, Jamage Industrial Estate, Talke Pits, Stoke-on-Trent, Staffordshire, ST7 1XW.
Marketing authorisation number
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