Equipalazone Injection 200mg/ml (50 ml pack)

Equipalazone Injection 200mg/ml (50  ml pack)
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Equipalazone 200 mg/ml solution for injection is indicated in the treatment of musculoskeletal disorders in horses and ponies where the anti-inflammatory and analgesic properties of phenylbutazone can offer relief against inflammation, pain and lameness. Read more
Equipalazone Injection 200mg/ml (50  ml pack)

Equipalazone 200 mg/ml solution for injection is indicated in the treatment of musculoskeletal disorders in horses and ponies where the anti-inflammatory and analgesic properties of phenylbutazone can offer relief against inflammation, pain and lameness.

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Product Description

About Equipalazone Injection 200mg/ml (50 ml pack)

Equipalazone Injection 200mg/ml (50  ml pack)

Equipalazone 200 mg/ml solution for injection is indicated in the treatment of musculoskeletal disorders in horses and ponies where the anti-inflammatory and analgesic properties of phenylbutazone can offer relief against inflammation, pain and lameness.

Please note: images are for illustration purposes only and pack sizes/strengths and new packaging styles may not be reflected in the image shown.

Directions For Use

Directions for Use

Horses: 450 kg (1000 lb) body weight:

Maximum 10 ml (4.4 mg phenylbutazone/kg).

Ponies: 225 kg (500 lb) body weight:

Maximum 5 ml (4.4 mg phenylbutazone/kg).

Equipalazone 200 mg/ml solution for injection should be administered by slow intravenous injection as a single dose, which may be followed if necessary by oral phenylbutazone therapy commencing 24 hours after the injection.

In acute cases and in hospitalised animals, Equipalazone 200 mg/ml solution for injection may be administered once daily for not more than five consecutive days.

Active Ingredient

Equipalazone Injection 200mg/ml (50 ml pack) ingredients

A sterile, aqueous solution for injection, containing phenylbutazone 200?mg/ml.

Side Effects

Side effects of Equipalazone Injection 200mg/ml (50 ml pack)

Not to be used in horses intended for human consumption. Treated horses may never be slaughtered for human consumption. The horse must have been declared as not intended for human consumption under national horse passport legislation.

The therapeutic index of phenylbutazone is low.

Do not exceed the stated dose or the duration of treatment.

There is a risk of irritancy if the injection is accidentally inoculated under the skin during intravenous injection.

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 a blood dyscrasia or hypersensitivity to the product.

Do not administer other NSAIDs concurrently or within 24 hours of each other.

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.

Use in animals less than six 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 any dehydrated, hypovolaemic or hypotensive animals as there is a risk of increased renal toxicity.

Concurrent administration of potentially nephrotoxic drugs should be avoided.

It is preferable that NSAIDs which inhibit prostaglandin synthesis are not administered to animals undergoing general anaesthesia until fully recovered.

Use during pregnancy should be avoided whenever possible, particularly during the first trimester.

Operator warnings: The product should be handled with care at all times to reduce the risk of accidental ingestion, skin contact or self-injection. If accidental skin or eye contact occurs, the site should be washed immediately with water. If the product is self-injected or ingested, seek medical advice and show the product packaging.

Advice to doctors: gastric lavage (emesis in children) should be performed urgently. Charcoal haemoperfusion has also been shown to be beneficial. Treatment should then be administered symptomatically.

General precautions: For animal treatment only.

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.

Rarely, collapse following intravenous injection has been reported. The product should be injected slowly over as long a period as is reasonably practical. At the first signs of intolerance, the administration of the injection should be interrupted.

Withdrawal period: Not to be used in horses intended for human consumption. Treated horses may never be slaughtered for human consumption. The horse must have been declared as not intended for human consumption under national horse passport legislation.

Additional Data

Equipalazone Injection 200mg/ml (50 ml pack) specification

Specification: Detail:
Pack Size: 50 ml pack
Brands: Dechra Veterinary
Product Form: injection
External Link: http://www.noahcompendium.co.uk/Dechra_Veterinary_Products/documents/S3408.html
Strength/Size: 200mg/ml

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Q & A

Q. if injected intraveneous, how long is bute traceable for in a horses blood.
A.

According to the FEI, bute administered by any route is detectable for approximately 7 days. Because this will vary from horse to horse (due to differences in metabolic rate, exercise, diet/other medications, underlying disease etc), it is the responsibility of the prescribing veterinary surgeon to determine a safe witholding time.

I hope that helps,

David Harris BVSc MRCVS
MyVetMeds

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