Losartan Cinfa 100 mg film-coated tablets EFG
Spain
Table of Contents
Patient Information Leaflet
Introduction
Patient Information Leaflet
losartán cinfa 100 mg film-coated tablets EFG
losartan potassium
Read the entire leaflet carefully before you start taking this medicine, as it contains important information for you.
- Keep this leaflet as you may need to read it again.
- If you have any questions, consult your doctor or nurse.
- This medicine has been prescribed for you only, and you should not give it to others, even if they have the same symptoms as you, because it may harm them.
- If you experience any adverse effects, consult your doctor or pharmacist, even if they are adverse effects not listed in this leaflet. See section 4.
Leaflet Contents
- What losartán cinfa is and what it is used for
- What you need to know before taking losartán cinfa
- How to take losartán cinfa
- Possible side effects
- How to store losartán cinfa
- Contents of the pack and other information
1. What is losartan cinfa and what is it used for
Losartan belongs to a group of medicines called angiotensin II receptor antagonists.
Angiotensin II is a substance produced in the body that binds to receptors in blood vessels, causing them to narrow. This leads to an increase in blood pressure.
Losartan blocks angiotensin II from binding to these receptors, causing blood vessels to relax, which in turn lowers blood pressure. Losartan slows the progression of impaired kidney function in patients with high blood pressure and type 2 diabetes.
losartan cinfa is used:
- to treat patients with high blood pressure (hypertension) in adults and in children and adolescents aged 6 to 18 years.
- to protect the kidneys in hypertensive patients with type 2 diabetes and laboratory test results indicating renal impairment and proteinuria ≥ 0.5 g per day (a condition in which the urine contains an abnormally high amount of protein).
- to treat patients with chronic heart failure when your doctor considers that treatment with specific medicines called angiotensin-converting enzyme (ACE) inhibitors (medicines used to lower high blood pressure) is not suitable. If your heart failure has been stabilized with an ACE inhibitor, you should not switch to losartan.
- in patients with high blood pressure and thickening of the left ventricle of the heart, losartan has been shown to reduce the risk of stroke (LIFE indication).
2. What you need to know before starting to take losartan cinfa
Do not take losartan cinfa
- If you are allergic to losartan or to any of the other ingredients of this medicine (listed in section 6).
- If you are more than 3 months pregnant. (It is also advisable to avoid losartan in early pregnancy (see section Pregnancy and breastfeeding).
- If your liver function is severely impaired.
- If you have diabetes or kidney failure and are being treated with an antihypertensive medicine containing aliskiren.
Warnings and precautions
Talk to your doctor or pharmacist before starting to take losartan cinfa.
Contact your doctor if you experience abdominal pain, nausea, vomiting, or diarrhea after taking losartan. Your doctor will decide whether to continue treatment. Do not stop taking losartan on your own.
You must inform your doctor if you think you are pregnant (or could be). Losartan is not recommended during early pregnancy, and should not be taken if you are more than three months pregnant, as it may cause serious harm to your baby if used during this stage (see section Pregnancy and breastfeeding).
Before taking losartan, it is important to inform your doctor:
- If you have previously had angioedema (swelling of the face, lips, tongue, and/or throat) (see also section 4. Possible side effects).
- If you are experiencing excessive vomiting or diarrhea, which may lead to excessive fluid and/or salt loss from your body.
- If you are taking diuretics (medicines that increase the amount of fluid passing through your kidneys) or are on a low-salt diet that may cause excessive fluid or salt loss from your body (see section 3, Dosage in special patient groups).
- If you know you have narrowing or blockage of the blood vessels supplying your kidneys or if you have recently undergone a kidney transplant.
- If your liver function is impaired (see sections 2. Do not take losartan cinfa and 3. Dosage in special patient groups).
- If you have heart failure with or without kidney impairment or potentially life-threatening concomitant cardiac arrhythmias. Special care is needed if you are also being treated with a beta-blocker.
- If you have heart valve problems or heart muscle disease.
- If you have coronary heart disease (caused by reduced blood flow in the heart's blood vessels) or cerebrovascular disease (caused by reduced blood circulation in the brain).
- If you have primary hyperaldosteronism (a syndrome associated with excessive secretion of the hormone aldosterone by the adrenal gland due to dysfunction of this gland).
- If you are taking any of the following medicines used to treat high blood pressure (hypertension):
- an angiotensin-converting enzyme inhibitor (ACE inhibitor) (e.g., enalapril, lisinopril, ramipril), particularly if you have kidney problems related to diabetes.
- aliskiren
Your doctor may monitor your kidney function, blood pressure, and blood levels of electrolytes (e.g., potassium) at regular intervals.
See also the information under the heading “Do not take losartan cinfa”.
- if you are taking other medicines that may increase serum potassium (see section 2 “Taking losartan cinfa with other medicines”).
Children and adolescents
Losartan has been studied in children. For further information, speak with your doctor.
Losartan is not recommended for use in children with kidney or liver problems, as there is limited data available in these patient groups. Losartan is not recommended for use in children under 6 years of age, as efficacy has not been demonstrated in this age group.
Taking losartan cinfa with other medicines
Inform your doctor or pharmacist if you are taking, have recently taken, or might need to take any other medicines.
Tell your doctor if you are taking potassium supplements, salt substitutes containing potassium, or potassium-sparing medicines such as certain diuretics (amiloride, triamterene, spironolactone), or other medicines that may increase serum potassium (e.g., heparin, medicines containing trimethoprim), as combination with losartan is not recommended.
While being treated with losartan, take particular care if you are taking any of the following medicines:
- Other medicines that lower blood pressure, as they may cause an additional reduction in blood pressure. Blood pressure may also be lowered by some of the following medicines/classes of medicines: tricyclic antidepressants, antipsychotics, baclofen, amifostine.
- Non-steroidal anti-inflammatory drugs (NSAIDs), such as indomethacin, including COX-2 inhibitors (medicines that reduce inflammation and may be used to relieve pain), as they may reduce the blood pressure-lowering effect of losartan.
Your doctor may need to adjust your dose and/or take other precautions:
If you are taking an angiotensin-converting enzyme inhibitor (ACE inhibitor) or aliskiren (see also the information under the headings “Do not take losartan cinfa” and “Warnings and precautions”).
If you have impaired kidney function, concomitant use of these medicines may lead to worsening of kidney function.
Medicines containing lithium should not be used in combination with losartan unless your doctor closely monitors you. Special precautionary measures (e.g., blood tests) may be appropriate.
Taking losartan cinfa with food and drink
Losartan can be taken with or without food.
Pregnancy and breastfeeding
Pregnancy
Inform your doctor if you think you are pregnant (or could be). Normally, your doctor will advise you to stop taking losartan before becoming pregnant or as soon as you know you are pregnant, and will recommend an alternative medicine to losartan. Losartan is not recommended during 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 after the third month of pregnancy.
Breastfeeding
Inform your doctor if you are breastfeeding or about to start breastfeeding. Losartan is not recommended for breastfeeding mothers, and your doctor may choose a different treatment for you if you wish to breastfeed. This is especially important if your baby is a newborn or was born prematurely.
Consult your doctor or pharmacist before using this medicine.
Driving and using machines
No studies on the effects on the ability to drive and use machines have been performed.
It is unlikely that losartan will affect your ability to drive or use machines. However, like many medicines used to treat high blood pressure, losartan may cause dizziness or drowsiness in some people. If you experience dizziness or drowsiness, consult your doctor before engaging in such activities.
losartan cinfa contains lactose.
If your doctor has informed you of an intolerance to certain sugars, consult him before taking this medicine.
3. How to take losartan cinfa
Follow exactly the instructions for using this medicine as given by your doctor or pharmacist. If you are unsure, consult your doctor or pharmacist again.
Your doctor will determine the appropriate dose of losartan, depending on your condition and whether you are taking other medicines. It is important to continue taking losartan as prescribed by your doctor to maintain consistent blood pressure control.
Adult patients with high blood pressure
Treatment usually starts with 50 mg of losartan (one losartan cinfa 50 mg tablet) once daily. The maximum blood pressure-lowering effect is reached within 3 to 6 weeks after starting treatment. Afterwards, in some patients, the dose may be increased to 100 mg of losartan (two losartan cinfa 50 mg tablets or one losartan cinfa 100 mg tablet) once daily.
If you feel that the effect of losartan is too strong or too weak, please inform your doctor or pharmacist.
Use in children and adolescents
Children under 6 years of age
Losartan is not recommended for use in children under 6 years of age, as its effectiveness has not been demonstrated in this age group.
Children aged between 6 and 18 years
The recommended starting dose for patients weighing between 20 and 50 kg is 0.7 mg of losartan per kg of body weight, given once daily (up to a maximum of 25 mg of losartan). The doctor may increase the dose if blood pressure is not adequately controlled.
Other pharmaceutical forms of this medicine may be more suitable for children; please consult your doctor or pharmacist.
Adult patients with high blood pressure and type 2 diabetes
Treatment usually starts with 50 mg of losartan (one losartan cinfa 50 mg tablet) once daily. Afterwards, the dose may be increased to 100 mg of losartan (two losartan cinfa 50 mg tablets or one losartan cinfa 100 mg tablet) once daily, depending on your blood pressure response.
Losartan may be administered together with other medicines that lower blood pressure (e.g., diuretics, calcium channel blockers, alpha or beta blockers, and centrally acting agents), as well as with insulin and other commonly used glucose-lowering medicines (e.g., sulfonylureas, glitazones, and alpha-glucosidase inhibitors).
Adult patients with heart failure
Treatment usually starts with 12.5 mg of losartan (one losartan cinfa 12.5 mg initiation tablet) once daily. The dose is typically increased gradually on a weekly basis (i.e., 12.5 mg daily during the first week, 25 mg daily during the second week, 50 mg daily during the third week, 100 mg daily during the fourth week, and 150 mg daily during the fifth week), up to a maintenance dose determined by your doctor. A maximum dose of 150 mg of losartan (e.g., three losartan cinfa 50 mg tablets or one losartan cinfa 100 mg tablet plus one losartan cinfa 50 mg tablet) once daily may be used.
In the treatment of heart failure, losartan is usually combined with a diuretic (a medicine that increases the amount of fluid passing through your kidneys) and/or digitalis (a medicine that helps your heart to become stronger and more efficient) and/or a beta-blocker.
Dosage in special patient groups
Your doctor may recommend a lower dose, especially when starting treatment in certain patients, such as those receiving high-dose diuretics, patients with hepatic impairment, or patients over 75 years of age. The use of losartan is not recommended in patients with severe hepatic impairment (see section "Do not take losartan cinfa").
Administration
The tablets should be swallowed whole with a glass of water. You should try to take your daily dose at approximately the same time each day. It is important that you continue taking losartan until your doctor tells you otherwise.
If you take more losartan cinfa than you should
If you accidentally take too many tablets, contact your doctor immediately. Symptoms of overdose may include low blood pressure, increased heart rate, and possibly decreased heart rate.
In case of overdose or accidental ingestion, contact your doctor, pharmacist, or call the Toxicology Information Service at telephone number 91 562 04 20, indicating the medicine and the amount ingested.
If you forget to take losartan cinfa
If you accidentally miss a dose, simply take the next dose as scheduled. Do not take a double dose to make up for the missed dose.
If you have any further questions about the use of this medicine, ask your doctor, pharmacist, or nurse.
4. Possible adverse effects
Like all medicines, this medicine can cause adverse effects, although not everyone experiences them.
If you experience the following, stop taking losartan tablets immediately and contact your doctor right away or go to the nearest hospital emergency department:
- A severe allergic reaction (rash, itching, swelling of the face, lips, mouth or throat, which may cause difficulty swallowing or breathing).
This is a serious but rare adverse effect, which may affect up to 1 in 1,000 patients. It may require urgent medical attention or hospitalization.
Adverse effects of medicines are classified according to the following:
The following adverse effects have been reported with losartan:
Common (may affect up to 1 in 10 patients):
- dizziness,
- low blood pressure (especially after excessive loss of fluid from the bloodstream, for example in patients with severe heart failure or those on high-dose diuretic therapy),
- dose-related orthostatic effects, such as a drop in blood pressure occurring after standing up from lying down or sitting,
- weakness,
- fatigue,
- low blood sugar (hypoglycaemia),
- high potassium levels in the blood (hyperkalaemia),
- changes in liver function, including renal failure,
- reduced number of red blood cells (anaemia),
- increased blood urea, creatinine and serum potassium levels in patients with heart failure.
Uncommon (may affect up to 1 in 100 patients):
- drowsiness,
- headache,
- sleep disorders,
- sensation of very rapid heartbeat (palpitations),
- severe chest pain (angina),
- difficulty breathing (dyspnoea),
- abdominal pain,
- constipation,
- diarrhoea,
- nausea,
- vomiting,
- hives (urticaria),
- itching (pruritus),
- rash,
- localized swelling (oedema),
- cough.
Rare (may affect up to 1 in 1,000 patients):
- hypersensitivity,
- angioedema,
- inflammation of blood vessels (vasculitis, including Schönlein-Henoch purpura),
- numbness or tingling sensation (paraesthesia),
- fainting (syncope),
- very rapid and irregular heartbeats (atrial fibrillation),
- stroke (cerebrovascular accident),
- liver inflammation (hepatitis),
- elevated levels of alanine aminotransferase (ALT) in blood, which usually resolves upon discontinuation of treatment,
- intestinal angioedema: swelling in the intestine causing symptoms such as abdominal pain, nausea, vomiting and diarrhoea.
Frequency not known (cannot be estimated from available data):
- reduced number of platelets,
- migraine,
- abnormalities in liver function,
- muscle and joint pain,
- flu-like symptoms,
- back pain and urinary tract infection,
- increased sensitivity to sunlight (photosensitivity),
- unexplained muscle pain with dark-coloured urine (tea-coloured) (rhabdomyolysis),
- impotence,
- inflammation of the pancreas (pancreatitis),
- low sodium levels in blood (hyponatraemia),
- depression,
- general feeling of being unwell (malaise),
- ringing, buzzing, noise or clicking in the ears (tinnitus),
- altered taste (dysgeusia).
Adverse effects in children are similar to those observed in adults.
Reporting of adverse effects
If you experience any adverse effect, talk to your doctor or pharmacist, even if it is a possible adverse effect not listed in this leaflet. You can also report them directly via the Spanish Pharmacovigilance System for Human Medicines: https://www.notificaram.es. By reporting adverse effects, you can help provide more information on the safety of this medicine.
5. Storage of losartan cinfa
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date stated on the packaging after EXP. The expiry date is the last day of the month indicated.
This medicine does not require any special storage conditions.
Store in the original container.
Do not open the blister pack until ready to take the medicine.
Medicines must not be disposed of via wastewater or household waste. Return any unused medicines and their containers to the SIGRE point at your pharmacy. If you are in doubt, ask your pharmacist how to dispose of medicines and containers you no longer need. This will help protect the environment.
6. Package contents and other information
Composition of losartán cinfa
- The active substance is potassium losartan. Each losartán cinfa 100 mg film-coated tablet contains 100 mg of potassium losartan.
- The other components are: monohydrate lactose, pregelatinized corn starch, microcrystalline cellulose, magnesium stearate, hydroxypropylcellulose, hydroxypropylmethylcellulose, and titanium dioxide (E-171).
losartán cinfa 100 mg contains potassium in the following amount: 8.48 mg (0.22 mEq).
Appearance of the medicinal product and contents of the pack
The losartán cinfa film-coated tablets are cylindrical and white in color.
losartán cinfa is available in aluminum-PVC/PVDC blisters, in pack sizes of 28 or 500 tablets (clinical pack).
Only certain pack sizes may be marketed.
Marketing Authorization Holder and Manufacturer:
Laboratorios Cinfa, S.A.
Carretera Olaz-Chipi, 10. Polígono Industrial Areta
31620 Huarte (Navarra) – Spain
Date of the most recent revision of this package leaflet: February 2025
Detailed information on this medicinal product is available on the website of the Spanish Agency of Medicines and Health Products (AEMPS) http://www.aemps.gob.es
You can access detailed and up-to-date information on this medicinal product by scanning with your mobile phone (smartphone) the QR code included in the package leaflet and outer packaging. You can also access this information at the following internet address: https://cima.aemps.es/cima/dochtml/p/67731/P_67731.html
QR code link: https://cima.aemps.es/cima/dochtml/p/67731/P_67731.html