Inflammatory Relief for Horses
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20gm Paste now available--ready to ship!
Anti-Inflammatory (not apple flavored)Description:
- Bute Paste is a synthetic, non-hormonal anti-inflammatory, anti-pyretic compound useful in the management of inflammatory conditions.
- The apparent analgesic effect is probably related mainly to the compound’s anti-inflammatory properties.
Paste dosage form makes the product ideal for dispensing.
- Orally – 1-2 grams of phenylbutazone per 500 lbs of body weight but, not to exceed 4 grams daily.
- Use a relatively high dose for the first 48 hours, then reduce gradually to a maintenance dose.
- Maintain lowest dose capable of producing desired clinical response.
- Response to ButePaste therapy is prompt, usually occurring within 24 hours.
- If no significant clinical response is evident after 5 days, reevaluate diagnosis and therapeutic approach.
- When administering ButePaste the oral cavity should be empty.
- Deposit paste on back of tongue by depressing plunger that has been previously set to deliver the correct dose.
- Many chronic conditions will respond to ButePaste therapy, but discontinuance of treatment may result in recurrence of symptoms.
Available in the popular 12 gram size, and now new 20 gram size.
Image shown may not be exact brand of Bute shipped.
EQUI-PHAR BUTEPASTE 20 GRAM
For Veterinary Use Only
ANADA 200-266, Approved by the FDA.
DESCRIPTION: Phenylbutazone Paste is a synthetic, non-hormonal, anti-inflammatory, antipyretic compound useful in the management of inflammatory conditions. The apparent analgesic effect is probably related mainly to the compound’s anti-inflammatory properties.
Chemically, Phenylbutazone Paste is 4-butyl-1, 2-diphenyl-3, 5-pyrazolidinedione. It is a pyrazolone derivative, entirely unrelated to the steroid hormones.
INDICATIONS: For the relief of inflammatory conditions associated with the musculoskeletal system in horses.
CONTRAINDICATIONS: Use with caution in patients who have a history of drug allergy.
WARNING: Not for use in horses intended for food.
PRECAUTIONS: Stop medication at the first sign of gastrointestinal upset, jaundice, or blood dyscrasia. Authenticated cases of agranulocytosis associated with the drug have occurred in man; fatal reactions, although rare, have been reported in dogs after long-term therapy. To guard against this possibility, conduct routine blood counts at weekly intervals during the early phase of therapy and at intervals of two weeks thereafter. Any significant fall in the total white blood cell count, relative decrease in granulocytes, or black or tarry stools, should be regarded as a signal for immediate cessation of therapy and institution of appropriate counter-measures. In the treatment of inflammatory conditions associated with infections, specific anti-infective therapy is required.
ADMINISTRATION AND DOSAGE: Orally - 1 to 2 g of phenylbutazone per 500 lb of body weight daily. Do not exceed 4 g daily.
Guidelines to Successful Therapy: Use a relatively high dose for the first 48 hours, then reduce gradually to a maintenance dose. Maintain lowest dose capable of producing desired clinical response. Response to Phenylbutazone Paste therapy is prompt, usually occurring within 24 hours. If no significant clinical response is evident after five days, re-evaluate diagnosis and therapeutic approach. When administering Phenylbutazone Paste, the oral cavity should be empty. Deposit paste on back of tongue by depressing plunger that has been previously set to deliver the correct dose. Many chronic conditions will respond to Phenylbutazone Paste therapy, but discontinuance of treatment may result in recurrence of symptoms.
STORAGE: Store at 15°-30°C (59°-86°F).
HOW SUPPLIED: Syringes containing 20 g of Phenylbutazone.
KEEP OUT OF REACH OF CHILDREN
CAUTION: Federal (U.S.A.) law restricts this drug to use by or on the order of a licensed veterinarian.
Each syringe contains 20 g phenylbutazone.
Each 3 mL marking on the plunger contains Phenylbutazone: 1 g.
Manufactured by: Med-Pharmex, Inc., Pomona, CA 91767-1861
Manufactured for: VEDCO, St. Joseph, MO 64507 USA
NAC No.: 10942872