Furosemide Tablets are a potent 'loop' diuretic used in the treatment of oedema resulting from cardiac insufficiency, hepatic or renal dysfunction, parasitism, or of a traumatic origin. They are most commonly used as part of the medical management of congestive heart failure and other conditions where the body is retaining too much fluid.
Furosemide Tablets are flat faced, white circular tablets with bevelled edges. They are scored with a half break line for accurate dosing.
£0.08Furosemide Tablets 20mg are indicated for the treatment of oedema associated with cardiac insufficiency, renal dysfunction, and trauma in cats and dogs. Furosemide is the most commonly used...
Furosemide Tablets 40mg are indicated for the treatment of oedema associated with cardiac insufficiency, renal dysfunction, and trauma in cats and dogs.
Contra-indicationsDo not use in acute glomerular nephritis, in electrolyte diseases, in patients with anuria, or patients that have received excessive doses of cardiac glycosides. Because of the danger of potentiating their toxic effects do not use with aminoglycoside or cephalosporin antibiotics. Allergic reactions have been associated with use with sulphonamides.
Special WarningsThe patient may increase its water intake to compensate for the diuresis. Consideration should be given to restricting water intake if the patient's condition makes such a course appropriate.
Special PrecautionsSpecial precautions for use in animals:Prolonged dosage may on occasions justify potassium supplementation and thus monitoring for hypokalaemia should be considered, especially if the product is used in conjunction with cardiac glycosides.Special precautions to be taken by the person administering the medicinal product to animals:Wear gloves or wash hands immediately after handling tablets. In case of accidental ingestion seek medical attention and show product label and/or pack insert to the doctor.
Adverse ReactionsNone reported
Pregnancy and LactationThe safety of use in pregnancy is not well established and a careful assessment of the likely benefits and potential risks should be made. A deleterious effect on lactation is to be expected, particularly if drinking water is restricted. Furosemide passes into milk, but not to a great extent.
InteractionsPotential interactions with other drugs include ototoxicity with aminoglycosides and nephrotoxicity with cephalosporins. Use in combination with sulphonamide treatment may lead to sulphonamide allergy. There is a possibility of interaction with cardiac glycosides.
Amounts to be Administered and Administration Route5mg/KgBW, one or two times per day. For patients weighing less than 8Kg dosage with the 20mg tablet (which may be halved) is recommended. Avoid overdosage in weak and old patients.
OverdoseDehydration and electrolyte depletion may occur. Monitor and correct, as necessary. Dosage higher than that which is recommended, may cause transitory deafness. Cardiovascular side effects may be observed in weak and old patients following overdose.
Withdrawal PeriodsNone for these species.
Forincible{"Active cephalosporin Stearate}{" time Stamp: Lower than Elsewhere Stamp: Lower than First Stamp: First Stig: First Sticky Stig: First Sticky Stig: First Sticky Stig: First Sticky Stig: Store at - 20 °C{"Instructions for use: Copy provided by patient. Each Kg of Stig contains 20mg of cefotaxime. Each Kg of cefotaxime contains 15mg of cefotaxime. Each Kg of cefotaxime contains 20mg of cefotaxime.Furosemide (Generic) Tabletsare a prescription medication used in dogs and cats to treat edema (fluid retention) and congestive heart failure. They belong to a class of medications called diuretics, which help the body remove excess fluid by increasing urine production. Furosemide tablets are available in various strengths and are typically given orally one to three times a day, as directed by a veterinarian. Furosemide is a potent diuretic that helps the body eliminate excess fluid, making it useful in the treatment of edema and congestive heart failure. Available in tablet form for easy oral administration to dogs and cats, furosemide is a prescription medication and should only be used under the guidance of a veterinarian. The dosage of furosemide varies depending on the pet's weight, condition, and other factors, so it is important to follow the veterinarian's instructions carefully. While generally safe when used as directed, furosemide can cause side effects such as increased thirst, increased urination, and electrolyte imbalances.
Furosemide (Generic) Tablets are indicated for the treatment of edema (fluid retention) associated with congestive heart failure, liver disease, or kidney disease in dogs and cats. They are also used to treat hypertension (high blood pressure) in some cases. Furosemide works by increasing the production of urine, which helps to remove excess fluid from the body. It is important to follow the veterinarian's instructions carefully when using furosemide to ensure its effectiveness and safety.
Furosemide (Generic) Tablets work as a diuretic by inhibiting the reabsorption of sodium and chloride in the kidneys. This action prevents the reabsorption of water, leading to increased urine production and the elimination of excess fluid from the body. By reducing the volume of fluid in the bloodstream, furosemide helps to decrease the workload on the heart and improve symptoms of edema, such as swelling and difficulty breathing, in conditions like congestive heart failure, liver disease, or kidney disease.
In the absence of a drug-specific pharmacokinetic property, the excretion of a single dose of furosemide is negligible in normal human body. The bioavailability of furosemide is approximately 2% in normal human body, with a terminal half-life of approximately 5–6 hours. The bioavailability of furosemide after oral administration of furosemide is approximately 97%. However, the plasma concentration and the half-life are longer in the presence of furosemide, possibly due to the lower water clearance.
Furosemide is rapidly excreted by the kidneys in the form of metabolites. It is then metabolized by hepatic enzymes and is the major active metabolites in normal human body.
After oral administration of furosemide, the clearance of furosemide is approximately 90%, with a terminal half-life of approximately 8–10 hours. The half-life of furosemide is approximately 3–4 hours. The maximum plasma concentration of furosemide is around 4 mg/mL and is not reached after oral administration of furosemide. The elimination half-life of furosemide is approximately 3–4 hours.
The metabolism of furosemide depends on the presence of a diuretic. The diuretic effect of furosemide is not observed in patients receiving furosemide in the absence of diuretics. The diuretic effect of furosemide in patients receiving furosemide in the absence of diuretics is similar to that of furosemide in the presence of other diuretics.
The half-life of furosemide is approximately 2 to 4 hours. The half-life of furosemide in normal human body is approximately 3 hours and is approximately 3–4 hours in the presence of furosemide.
Furosemide is rapidly and completely excreted from the body by the kidneys. The amount excreted by the kidneys is approximately 80%, with a terminal half-life of approximately 10 hours. The maximum plasma concentration of furosemide is approximately 2 mg/mL and is not reached after oral administration of furosemide. The elimination half-life of furosemide is approximately 3 hours and is approximately 3–4 hours in the presence of furosemide.
The half-life of furosemide is approximately 3 to 6 hours. The half-life of furosemide is approximately 4 hours and is approximately 4–6 hours in the presence of furosemide. The elimination half-life of furosemide is approximately 3 hours and is approximately 2 hours in the presence of furosemide.
The plasma half-life of furosemide is approximately 3 to 6 hours. The half-life of furosemide is approximately 4 hours and is approximately 3–6 hours in the presence of furosemide.
The plasma half-life of furosemide is approximately 2 to 4 hours.
Furosemide is metabolized by the liver. The hepatic metabolism of furosemide in the presence of furosemide is not significantly affected by the presence of other diuretics. The amount excreted in the urine is approximately 80% of the administered dose. The urine excretion rate is approximately 60% of the administered dose.
Furosemide is eliminated mainly by the kidneys. The amount of the active drug in the body is approximately 2 to 4 mg/mL. In the absence of a diuretic, the amount excreted by the kidneys is approximately 80%. The amount excreted by the kidneys is approximately 80%. The excretion rate is approximately 60% of the administered dose. The total amount of drug that is excreted in the body is about 2 to 4 mg/mL.
Furosemide is eliminated by the kidneys.
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