Agrovet Market S.A.

Diuride 500
 
Diuride 500

Generik Name

none

Komposition

Furosemide 50 mg; excipient q.s. ad 100 mL.

Verschreibung

Diuretic

Indikation

diuretic. indicated as coadjuvant in reduction of pulmonary and bronchial edema, of foreskin, scrotum, extremities and physiopathological edema of udder. Coadjuvant in elimination of inflammatory and non inflammatory pathological liquids of tissues and cavities (ascites, hidrothorax, hydropericardium).

Kontra-Indikationen

Do not use in case of tuberculosis, congestive cardiac insufficiency and severe hypertension, gastrointestinal ulcer, diabetes mellitus, chronic nephritis, viral, parasitic or mycotic diseases, bacterial dermatitis, ulcerous dermatitis, degenerative or traumatic ocular disorders, glaucoma, osteoporosis, renal failure, acute glomerulonephritis or acute renal failure, anuria; use with precaution on urination disorders. Hypersensibility to the formula compounds. Patients allergic to sulfonamides (sulfonamide or sulfonylureas antibiotics) can present cross sensitivity with furosemide. Hypovolemia or dehidratation. Anuric renal insufficiency that does not respond to furosemide. Severe hypocalcemia. Severe hyponatremia. Pre-coma and coma stages associated to hepatic encephalopathy. Hypersensitivity to sulfites or to any other compound of this product. Systemic mycosis.

Nebenwirkungen

Furosemide produces an increase on sodium and chlorides excretion, subsequently water. It also increases other electrolytes excretion, most of all potassium, calcium and magnesium. There can be symptomatic electrolytic disorders and metabolic alcalosis as an electrolytic deficit with gradual increase or acute electrolytic lost, when higher doses to animals with normal renal function are administered .

The furosemide diuretic action can cause or contribute to hypovolemia and dehidratation, specially in elder animals.

Furosemide can cause a drop in the arterial blood pressure, and if it is pronounced it can cause signs and symptoms associated to itself.

The increase of urine production can cause or get worst in animals with urine flow obstruction: there can be acute urine retention with possibly secondary complications in animals with vessel evacuations disorders, prostatic hyperplasia or urethra narrowness.

Occasionally there can be gastrointestinal reactions such as nausea, vomit or diarrheas. In isolated cases, there can be intrahepatic cholestasis, increase of hepatic transaminase or acute pancreatitis.

Occasionally there can be skin or mucosa reactions, such as rash, urticaria, eruptions or lesions, erythema multiforme and dermatitis.

Unusually anaphylactic or anaphylactoid reactions with shock can appear. There can be interstitial nephritis, vasculitis or eosinophilia, also fever or paresthesia and occasionally photosensitivity.

After the intramuscular administration there can be a local painful reaction.

Dosierung

Intramuscular route at a rate of 1 mL/50 Kg of body weight, ruminants: once a day; equines: twice a day. Minor animals: 0.25 mL-0.5 mL/5 Kg, once or twice a day.

Rückruf-Zeiten

USE RESTRICTIONS
The time that should pass between the last treatment and the animals sacrifice and/or milk use for human consumption is 48 hours since the last application. Do not use in horses destined to human consumption.

Verpackung

Glass vial of 20 mL, glass vial of 50 mL, glass vial of 100 mL.

Generelle Produktinformation

none