Country: United States
Language: English
Source: NLM (National Library of Medicine)
Dexamethasone (UNII: 7S5I7G3JQL) (Dexamethasone - UNII:7S5I7G3JQL)
Butler Animal Health Supply, LLC D/B/A Henry Schein Animal Health
INTRAMUSCULAR
PRESCRIPTION
INDICATIONS: DEXAJECT is indicated for the treatment of primary bovine ketosis and as an anti-inflammatory agent in the bovine and equine. As supportive therapy, DEXAJECT may be used in the management of various rheumatic, allergic, dermatologic, and other diseases known to be responsive to anti-inflammatory corticosteroids. DEXAJECT may be used intravenously as supportive therapy when an immediate hormonal response is required. Bovine Ketosis: DEXAJECT is offered for the treatment of primary ketosis. The gluconeogenic effects of DEXAJECT, when administered intramuscularly, are generally noted within the first 6 to 12 hours. When DEXAJECT is used intravenously, the effects may be noted sooner. Blood sugar levels rise to normal levels rapidly and generally rise to above normal levels within 12 to 24 hours. Acetone bodies are reduced to normal concentrations usually within 24 hours. The physical attitude of animals treated with DEXAJECT brightens and appetite improves, usually within 12 hours. Milk p
HOW SUPPLIED: DEXAJECT, 2 mg per mL, 100 mL multiple dose vial.
Abbreviated New Animal Drug Application
DEXAJECT- DEXAMETHASONE INJECTION, SOLUTION BUTLER ANIMAL HEALTH SUPPLY, LLC D/B/A HENRY SCHEIN ANIMAL HEALTH ---------- CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian DESCRIPTION: Dexamethasone Solution is a synthetic analogue of prednisolone, having similar but more potent anti-inflammatory therapeutic action and diversified hormonal and metabolic effects. Modification of the basic corticoid structure as acheived in DEXAJECT offers enhanced anti- inflammatory effect compared to older corticosteroids. The dosage of DEXAJECT required is markedly lower than that of prednisone and prednisolone. DEXAJECT is not species-specific; however, the veterinarian should read the sections on INDICATIONS, DOSAGE, SIDE EFFECTS, CONTRAINDICATIONS, PRECAUTIONS, and WARNINGS before this drug is used. DEXAJECT is intended for intravenous or intramuscular administration. Each mL contains 2 mg dexamethasone, 500 mg polyethylene glycol 400, 9 mg benzyl alcohol, 1.8 mg methylparaben and 0.2 mg propylparaben as preservatives, 4.75 percent alcohol, HCl to adjust pH to approximately 4.9, water for injection q.s. EXPERIMENTAL STUDIES: Experimental animal studies on dexamethasone have revealed it possesses greater anti-inflammatory activity than many steroids. Veterinary clinical evidence indicates dexamethasone has approximately 20 times the anti-inflammatory activity of prednisolone and 70 to 80 times that of hydrocortisone. Thymus involution studies show dexamethasone possesses 25 times the activity of prednisolone. In reference to mineralcorticoid activity, dexamethasone does not cause significant sodium or water retention. Metabolic balance studies show that animals on controlled and limited protein intake will exhibit nitrogen losses on exceedingly high dosages. INDICATIONS: DEXAJECT is indicated for the treatment of primary bovine ketosis and as an anti- inflammatory agent in the bovine and equine. As supportive therapy, DEXAJECT may be used in the management of various rheumatic, allerg Read the complete document