Country: United Kingdom
Language: English
Source: MHRA (Medicines & Healthcare Products Regulatory Agency)
Furosemide
Pinewood Healthcare
C03CA01
Furosemide
8mg/1ml
Oral solution
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 02020200; GTIN: 5099186003566
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you. - Keep this leaflet. You may need to read it again. - If you have any further questions, ask your doctor or pharmacist. - This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours. - If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4. What is in this leaflet: 1. What Furosemide is and what it is used for 2. What you need to know before you take Furosemide 3. How to take Furosemide 4. Possible side effects 5. How to store Furosemide 6. Contents of the pack and other information 1. WHAT FUROSEMIDE IS AND WHAT IT IS USED FOR Furosemide belongs to a group of medicines called diuretics which reduce excess water (fluid retention) in the body by increasing urine production. Water can accumulate if you have a condition affecting your heart, lungs, kidney, liver or blood vessels. Furosemide 40 mg/5 ml Oral Solution is particularly useful for patients who cannot take tablets. 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE FUROSEMIDE DO NOT take Furosemide: • if you are allergic to furosemide or any of the other ingredients of this medicine _(listed in section 6)._ Signs of an allergic reaction include: a rash, swallowing or breathing problems, swelling of your lips, face, throat or tongue • if you are allergic to sulphonamides or sulphonamide derivatives, such as sulfadiazine or cotrimoxazole • if you have a low blood volume or are dehydrated (with or without accompanying low blood pressure) • if you have too little potassium or sodium in your blood (shown in blood test) • if you have severe liver problems (cirrhosis) • if you have already taken furosemide in the past to treat failure to pass urine or kidney failure that is due to medicines or chemicals that are prone to cause kidney or liver damage or if you have Read the complete document
OBJECT 1 FUROSEMIDE 40 MG/5 ML ORAL SOLUTION Summary of Product Characteristics Updated 15-Nov-2017 | Pinewood Healthcare 1. Name of the medicinal product Furosemide 40 mg/5 ml Oral Solution 2. Qualitative and quantitative composition Each 5ml contains Furosemide 40 mg. Excipients with known effect Ethanol Liquid maltitol For the full list of excipients, see section 6.1. 3. Pharmaceutical form Oral Solution Clear, cherry flavoured, oral solution 4. Clinical particulars 4.1 Therapeutic indications Furosemide oral solution is indicated in all conditions requiring prompt diuresis in patients who are unable to take solid dose forms. Indications, include cardiac, pulmonary, hepatic and renal oedema, peripheral oedema due to mechanical obstruction or venous insufficiency and hypertension. 4.2 Posology and method of administration Posology Furosemide 40mg/5ml has an exceptionally wide therapeutic range, the effect being proportional to the dosage. Furosemide 40mg/5ml is best given as a single dose either daily or on alternate days. The recommended initial daily dose is 40mg. This may require adjustment until the effective dose is achieved as a maintenance dose. In mild cases, 20mg daily or 40mg on alternate days may be sufficient, whereas in cases of resistant oedema, daily doses of 80mg and above may be used as one or two dose daily, or intermittently. Severe cases may require gradual titration of the furosemide dosage up to 600mg daily. The recommended maximum daily dose of furosemide administration is 1500mg. _Elderly:_ The dosage recommendations for adults apply, but in the elderly, furosemide is generally eliminated more slowly. Dosage should be titrated until the required response is achieved. _Children:_ Oral doses for children range from 1 to 3 mg/Kg body weight daily up to a maximum total dose of 40 mg/day. 4.3 Contraindications Hypersensitivity to the active substance or to any of the excipients listed in section 6.1. Hypersensitivity to sulphonamides or sulphonamide derivatives. Hypovolaemia and dehydration ( Read the complete document