LOSARTAN POTASSIUM 100 MG FILM-COATED TABLETS

Active substance: LOSARTAN POTASSIUM

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PACKAGE LEAFLET: INFORMATION FOR THE USER

Losartan potassium 12.5 mg Losartan potassium 25 mg Losartan potassium 50 mg Losartan potassium 100 mg
film-coated tablets Losartan potassium
Read all of this leaflet carefully before you start taking this medicine. 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. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours. If any of the side effects gets serious or if you note any side effects not listed in this leaflet, please tell your doctor or pharmacist. In this leaflet: 1. What Losartan potassium is and what it is used for 2. Before you take Losartan potassium 3. How to take Losartan potassium 4. Possible side effects 5. How to store Losartan potassium 6. Further information 1. WHAT Losartan potassium IS AND WHAT IT IS USED FOR Losartan belongs to a group of medicines known as angiotensin-II receptor antagonists. Angiotensin-II is a substance produced in the body which binds

film-coated tablets film-coated tablets film-coated tablets

to receptors in blood vessels, causing them to tighten. This results in an increase in blood pressure. Losartan prevents the binding of angiotensin-II to these receptors, causing the blood vessels to relax which in turn lowers the blood pressure. Losartan slows the decrease of kidney function in patients with high blood pressure and type 2 diabetes. Losartan potassium is used to treat patients with high blood pressure (hypertension) to protect the kidney in hypertensive type 2 diabetic patients with laboratory evidence of impaired renal function and proteinuria 0.5 g per day (a condition in which urine contains an abnormal amount of protein). to treat patients with chronic heart failure when therapy with specific medicines called angiotensin-converting-enzyme inhibitors (ACE inhibitors, medicine used to lower high blood pressure) is not considered suitable by your doctor. If your heart failure has been stabilised with an ACE inhibitor you should not be switched to losartan. in patients with high blood pressure and a thickening of the left ventricle, losartan has been shown to decrease the risk of stroke (LIFE indication). 2. Before you take Losartan potassium Do not take Losartan potassium if you are allergic (hypersensitive) to losartan or to any of its other ingredients; if your liver function is severely impaired; if you are more than 3 months pregnant. (It is also better to avoid Losartan potassium in early pregnancy see pregnancy section). Take special care with Losartan potassium It is important to tell your doctor before taking Losartan potassium: if you have had a history of angiooedema (swelling of the face, lips, throat, and/or tongue) (see also section 4 Possible side effects), if you suffer from excessive vomiting or diarrhoea leading to an extreme loss of fluid and/or salt in your body, if you receive diuretics (medicines that increase the amount of water that you pass out through your kidneys) or are under dietary salt restriction

leading to an extreme loss of fluid and salt in your body (see section 3 Dosage in special patient groups), if you are known to have narrowing or blockage of the blood vessels leading to your kidneys or if you have received a kidney transplant recently, if your liver function is impaired (see sections 2 Do not take Losartan and 3 Dosage in special patient groups), if you suffer from heart failure with or without renal impairment or concomitant severe life threatening cardiac arrhythmias. Special caution is necessary when you are treated with a -blocker concomitantly, if you have problems with your heart valves or heart muscle, if you suffer from coronary heart disease (caused by a reduced blood flow in the blood vessels of the heart) or from cerebrovascular disease (caused by a reduced blood circulation in the brain), if you suffer from primary hyperaldosteronism (a syndrome associated with increased secretion of the hormone aldosterone by the adrenal gland, caused by an abnormality within the gland). You must tell your doctor if you think you are (or might become) pregnant. Losartan potassium is not recommended in early pregnancy and must not be taken if you are more than 3 months pregnant, as it may cause serious harm to your baby if used at that stage (see pregnancy section). Taking other medicines Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription or herbal medicines and natural products. Take particular care if you are taking the following medicines while under treatment with Losartan potassium : other blood pressure lowering medicines as they may additionally reduce your blood pressure. Blood pressure may also be lowered by one of the following drugs/ class of drugs: tricyclic antidepressants, antipsychotics, baclofen, amifostine, medicines which retain potassium or may increase potassium levels (e.g. potassium supplements, potassium-containing salt substitutes or potassium-sparing medicines such as certain diuretics [amiloride, triamterene, spironolactone] or heparin),

non-steroidal anti-inflammatory drugs such as indometacin, including COX-2-inhibitors (medicines that reduce inflammation, and can be used to help relieve pain) as they may reduce the blood lowering effect of losartan. If your kidney function is impaired, the concomitant use of these medicines may lead to a worsening of the kidney function. Lithium containing medicines should not be taken in combination with losartan without close supervision by your doctor. Special precautionary measures (e.g. blood tests) may be appropriate. Taking Losartan potassium with food and drink Losartan potassium may be taken with or without food. Pregnancy and breast-feeding Ask your doctor or pharmacist for advice before taking any medicine. Pregnancy You must tell your doctor if you think you are (or might become) pregnant. Your doctor will normally advise you to stop taking Losartan potassium before you become pregnant or as soon as you know you are pregnant and will advise you to take another medicine instead of Losartan potassium. Losartan potassium is not recommended in early pregnancy and must not be taken when more than 3 months pregnant, as it may cause serious harm to your baby if used after the third month of pregnancy. Breast-feeding Tell your doctor if you are breast-feeding or about to start breast-feeding. Losartan potassium is not recommended for mothers who are breast-feeding and your doctor may choose another treatment for you if you wish to breast-feed, especially if your baby is newborn, or was born prematurely. Use in children and adolescents Losartan has been studied in children. For more information, talk to your doctor. Driving and using machines No studies on the effects on the ability to drive and use machines have been performed. Losartan is unlikely to affect your ability to drive or use machines. However, as with many other medicines used to treat high blood pressure,

losartan may cause dizziness or drowsiness in some people. If you experience dizziness or drowsiness, you should consult your doctor before attempting such activities. Important information about some of the ingredients of Losartan potassium This product contains lactose. If you have been told by your doctor that you have intolerance to some sugars, contact your doctor before taking this medicinal product. 3. How to take Losartan potassium Always take Losartan potassium exactly as your doctor has instructed you. Your doctor will decide on the appropriate dose of Losartan potassium, depending on your condition and whether you are taking other medicines. It is important to continue taking Losartan potassium for as long as your doctor prescribes it in order to maintain smooth control of your blood pressure. Losartan-potassium containing medicinal products are available in the following strengths: 12.5 mg, 25 mg, 50 mg and 100 mg. Patients with High Blood Pressure Treatment usually starts with 50 mg losartan (one tablet of Losartan potassium 50 mg) once a day. The maximal blood pressure lowering effect should be reached 3-6 weeks after beginning treatment. In some patients the dose may later be increased to 100 mg losartan (two tablets of Losartan potassium 50 mg) once daily. If you have the impression that the effect of losartan is too strong or too weak, please talk to your doctor or pharmacist. Patients with high blood pressure and type 2 diabetes Treatment usually starts with 50 mg losartan (one tablet of Losartan potassium 50 mg) once a day. The dose may later be increased to 100 mg losartan (two tablets of Losartan potassium 50 mg) once daily depending on your blood pressure response. Losartan tablets may be administered with other blood pressure lowering medicines (e.g. diuretics, calcium channel blockers, alpha- or beta-blockers, and centrally acting agents) as well as with insulin and other commonly used

medicines that decrease the level of glucose in the blood (e.g. sulfonylureas, glitazones and glucosidase inhibitors). Patients with Heart Failure Treatment usually starts with 12.5 mg losartan (one tablet of Losartan potassium 12.5 mg) once a day. Generally, the dose should be increased weekly step-by-step (i.e., 12.5 mg daily during the first week, 25 mg daily during the second week, 50 mg daily during the third week) up to the usual maintenance dose of 50 mg losartan (one tablet of Losartan potassium 50 mg) once daily, according to your condition. In the treatment of heart failure, losartan is usually combined with a diuretic (medicine that increases the amount of water that you pass out through your kidneys) and/or digitalis (medicine that helps to make the heart stronger and more efficient) and/or a beta-blocker. Dosage in special patient groups The doctor may advise a lower dose, especially when starting treatment in certain patients such as those treated with diuretics in high doses, in patients with liver impairment, or in patients over the age of 75 years. The use of losartan is not recommended in patients with severe hepatic impairment (see section Do not take losartan). Administration The tablets should be swallowed with a glass of water. You should try to take your daily dose at about the same time each day. It is important that you continue to take Losartan potassium until your doctor tells you otherwise. If you take more Losartan potassium than you should If you accidentally take too many tablets, or a child swallows some, contact your doctor immediately. Symptoms of overdose are low blood pressure, increased heartbeat, possibly decreased heartbeat. If you forget to take Losartan potassium If you accidentally miss a daily dose, just take the next dose as normal. Do not take a double dose to make up for a forgotten tablet. If you have any further questions on the use of this product, ask your doctor or pharmacist.

4. POSSIBLE SIDE EFFECTS Like all medicines, Losartan potassium can cause side effects, although not everybody gets them. Side effects may occur with certain frequencies, which are defined as follows: Very common Common Uncommon Rare Very rare Not known affects more than 1 user in 10 affects 1 to 10 users in 100 affects 1 to 10 users in 1,000 affects 1 to 10 users in 10,000 affects less than 1 user in 10,000 frequency cannot be estimated from the available data

If you experience the following, stop taking losartan tablets and tell your doctor immediately or go to the casualty department of your nearest hospital: A severe allergic reaction (rash, itching, swelling of the face, lips, mouth or throat that may cause difficulty in swallowing or breathing). This is a serious but rare side effect, which affects more than 1 out of 10,000 patients but less than 1 out of 1,000 patients. You may need urgent medical attention or hospitalisation. The following side effects have been reported with losartan: Common: dizziness, low blood pressure, debility, fatigue, too little sugar in the blood (hypoglycaemia), too much potassium in the blood (hyperkalaemia). Uncommon: somnolence, headache, sleep disorders,



feeling of increased heart rate (palpitations), severe chest pain (angina pectoris), low blood pressure (especially after excessive loss of water from the body within blood vessels e.g. in patients with severe heart failure or under treatment with high dose diuretics), dose-related orthostatic effects such as lowering of blood pressure appearing when rising from a lying or sitting position, shortness of breath (dyspnoea), abdominal pain, obstipation, diarrhoea, nausea, vomiting, hives (urticaria), itching (pruritus), rash, localised swelling (oedema).

increase in blood urea, serum creatinine and serum potassium in patients with heart failure, back pain and urinary tract infection. If any of the side effects gets serious or if you note any side effect not listed in this leaflet, please tell your doctor or pharmacist. 5. How to store Losartan potassium Keep out of the reach and sight of children. Do not use Losartan potassium after the expiry date which is stated on the carton after EXP. The expiry date refers to the last day of that month. This medicinal product does not require any special storage conditions. Medicines should not be disposed of via waste water or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment. 6. FURTHER INFORMATION What Losartan potassium contains The active substance is Losartan potassium. Each film-coated tablet contains 12.5 mg, 25 mg, 50 mg or 100 mg Losartan potassium, equivalent to 11.4 mg, 22.9 mg, 45.8 mg and 91.5 mg losartan respectively. The other ingredients of Losartan potassium 12.5 mg/25 mg are: maize starch, pregelatinised maize starch, microcrystalline cellulose, colloidal anhydrous silica, magnesium stearate, cellactose (powdered cellulose and lactose monohydrate) in the tablet core and hypromellose, talc, propylene glycol, titanium dioxide (E171) and quinoline yellow (E104) in the film coating. The other ingredients of Losartan potassium 50 mg/100 mg are: maize starch, pregelatinised maize starch, microcrystalline cellulose, colloidal anhydrous silica, magnesium stearate, cellactose (powdered cellulose and lactose monohydrate) in the tablet core and hypromellose, talc, propylene glycol and titanium dioxide (E171) in the film coating.

What Losartan potassium looks like and contents of the pack Losartan potassium 12.5 mg: Oval, convex, yellow, film-coated tablet. Losartan potassium 25 mg: Oval, convex, yellow, film-coated, one-side-scored tablet. The tablet can be divided into equal halves. Losartan potassium 50 mg: Round, convex, white film-coated, one-side-scored tablet with bevelled edges. The tablet can be divided into equal halves. Losartan potassium 100 mg: Oval, convex, white film-coated tablet. Losartan potassium 12.5 mg/25 mg/50 mg/100 mg PVC/PVDC blister of transparent foil, with aluminium foil used for covering; box. Pack sizes: Losartan potassium 12.5 mg: 7, 10, 14, 15, 20, 21, 28, 30, 50, 56, 60, 84, 90, 98, 100 film-coated tablets, Losartan potassium 25 mg: 10, 14, 15, 20, 28, 30, 50, 56, 60, 84, 90, 98, 100 film-coated tablets, Losartan potassium 50 mg: 10, 14, 15, 20, 28, 30, 50, 56, 60, 84, 90, 98, 100 film-coated tablets, Losartan potassium 100 mg: 7, 10, 14, 15, 20, 28, 30, 50, 56, 60, 84, 90, 98, 100 film-coated tablets. Losartan potassium 50 mg Polyethylene (HDPE) tablet container with polypropylene closure. Polyethylene dessicator filled with silica gel. Pack size: 250 film-coated tablets. Not all the pack sizes may be marketed. Marketing Authorisation Holder: Krka d.d., marjeka cesta 6, 8501 Novo mesto, Slovenia Manufactured by: 1. KRKA, d.d., Novo mesto, marjeka cesta 6, 8501 Novo mesto, Slovenia 2. TAD Pharma GmbH, Heinz-Lohmann-Strae 5, 27472 Cuxhaven, Germany Distributed by: Consilient Health (UK) Ltd., 500 Chiswick High Road, London, W4 5RG. This leaflet was last revised in December 2011
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Rare: inflammation of blood vessels (vasculitis including Henoch-Schonlein purpura), numbness or tingling sensation (paraesthesia), fainting (syncope), very rapid and irregular heartbeat (atrial fibrillation) brain attack (stroke), inflammation of the liver (hepatitis), elevated blood alanine aminotransferase (ALT) levels, usually resolved upon discontinuation of treatment. Not known: reduced number of red blood cells (anaemia), reduced number of thrombocytes, migraine, cough, liver function abnormalities, muscle and joint pain, changes in kidney function (may be reversible upon discontinuation of treatment) including kidney failure, flu-like symptoms,

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Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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