Enalapril Aurovitas 10 mg tablets

Package leaflet: Information for the user

Introduction

Package leaflet: information for the user

Enalapril Aurovitas 10 mg tablets

enalapril maleate

Read the entire 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 questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you only. Do not pass it on to other people, 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 effects not listed in this leaflet. See section 4.

Contents of the leaflet

1. What Enalapril Aurovitas is and what it is used for

2. What you need to know before taking Enalapril Aurovitas

3. How to take Enalapril Aurovitas

4. Possible side effects

5. How to store Enalapril Aurovitas

6. Contents of the pack and other information

1. What Enalapril Aurovitas is and what it is used for

Enalapril Aurovitas contains an active substance called enalapril maleate. It belongs to a group of medicines known as ACE inhibitors (angiotensin-converting enzyme inhibitors).

Enalapril is used to:

• Treat high blood pressure (hypertension)
• Treat heart failure (weakening of the heart's function). It may reduce the need for hospitalization and may help some patients live longer
• Prevent signs of heart failure. Signs include: shortness of breath, tiredness after mild physical activity such as walking, or swelling of the ankles and feet.

This medicine works by widening your blood vessels. This lowers your blood pressure. The medicine usually starts to work within one hour and its effect lasts for at least 24 hours. Some people may need several weeks of treatment before the full effect on blood pressure is seen.

2. What you need to know before taking Enalapril Aurovitas

Do not take Enalapril Aurovitas

• If you are allergic to enalapril maleate or any of the other ingredients of this medicine (listed in section 6).
• If you have ever been treated for an allergic reaction to a medicine similar to this one, called an ACE inhibitor.
• If you have ever had swelling of the face, lips, mouth, tongue or throat that caused difficulty swallowing or breathing (angioedema) when the cause was unknown or hereditary.
• If you have diabetes or kidney failure and are being treated with a blood pressure-lowering medicine containing aliskiren.
• If you are more than 3 months pregnant. (It is also advisable to avoid enalapril in early pregnancy – see Pregnancy section.)
• If you are currently taking or have recently taken sacubitril/valsartan, a medicine used to treat chronic heart failure in adults, as the risk of angioedema (rapid swelling beneath the skin, such as in the throat) is high.
• If you are currently taking any of the following medicines, the risk of developing angioedema may increase:
  • Racecadotril, a medicine used to treat diarrhoea.
  • Medicines used to prevent organ transplant rejection and for cancer (e.g., temsirolimus, sirolimus, everolimus).
• Vildagliptin, a medicine used to treat diabetes.

Do not take this medicine if any of the above apply to you. If you are unsure, consult your doctor or pharmacist before starting to take this medicine.

Warnings and precautions

Consult your doctor or pharmacist before starting to take Enalapril Aurovitas:

• If you have a heart condition.
• If you have a disease affecting the blood vessels in the brain.
• If you have blood disorders such as low or absent white blood cells (neutropenia/agranulocytosis), low platelet count (thrombocytopenia), or low red blood cell count (anaemia).
• If you have a liver problem.
• If you have a kidney problem (including after kidney transplant). This may lead to high levels of potassium in your blood, which can be serious. Your doctor may need to adjust your enalapril dose or monitor your blood potassium levels.
• If you are undergoing dialysis.
• If you have recently experienced excessive vomiting or severe diarrhoea.
• If you are on a salt-free diet, taking potassium supplements, potassium-sparing medicines, salt substitutes containing potassium, or other medicines that may increase blood potassium levels, such as heparin (a medicine used to prevent blood clots), medicines containing trimethoprim or cotrimoxazole (also known as trimethoprim/sulfamethoxazole), which are used to treat infections.
• If you are over 70 years old.
• If you have diabetes. You should monitor your blood for low blood glucose levels, especially during the first month of treatment. Your blood potassium levels may also be higher.
• If you have ever had an allergic reaction with swelling of the face, lips, tongue or throat causing difficulty swallowing or breathing. Please note that black patients have a higher risk of such reactions to ACE inhibitors.
• If you have low blood pressure (you may feel faint or dizzy, especially when standing up).
• If you have a vascular collagen disease (e.g., systemic lupus erythematosus, rheumatoid arthritis or scleroderma), are being treated with medicines that suppress your immune system, or are taking allopurinol, procainamide, or any combination of these.
• If you are taking an mTOR inhibitor (e.g., temsirolimus, sirolimus, everolimus: medicines used to treat certain cancers or to prevent rejection of transplanted organs) or a medicine containing a neprilysin inhibitor such as sacubitril (available in a fixed-dose combination with valsartan), used in patients with heart failure, or racecadotril, used in patients with acute diarrhoea. You may have an increased risk of an allergic reaction called angioedema.
• If you are taking any of the following medicines for high blood pressure (hypertension):
  • An angiotensin II receptor antagonist (ARA) (also known as “sartans” – e.g., valsartan, telmisartan, irbesartan), particularly if you have kidney problems related to diabetes.
  • Aliskiren.

Your doctor may regularly monitor your kidney function, blood pressure, and blood electrolyte levels (e.g., potassium).

See also the information under the heading “Do not take Enalapril Aurovitas”.

Inform your doctor if you think you are pregnant (or could be). This medicine is not recommended in early pregnancy and must not be taken after the third month of pregnancy, as it may cause serious harm to your baby if used during this period (see Pregnancy section).

Please note that this medicine is less effective in lowering blood pressure in black patients compared to non-black patients.

If you are unsure whether any of the above apply to you, consult your doctor or pharmacist before starting to take this medicine.

If you are about to undergo a procedure

If you are about to undergo any of the following procedures, inform your doctor that you are taking enalapril:

• Any surgery or if you are to receive anaesthetics (including at the dentist).
• A treatment to remove cholesterol from your blood called “LDL apheresis”.
• A desensitisation treatment to reduce the effect of an allergy to bee or wasp stings.

If any of the above apply to you, consult your doctor or dentist before starting the procedure.

Taking Enalapril Aurovitas with other medicines

Inform your doctor or pharmacist if you are taking, have recently taken, or might need to take any other medicines. This includes herbal remedies. This is because enalapril may affect how other medicines work, and other medicines may affect how enalapril works. Your doctor may need to adjust your dose and/or take other precautions.

In particular, inform your doctor or pharmacist if you are taking any of the following medicines:

• An angiotensin II receptor antagonist (ARA) or aliskiren (see also information under “Do not take Enalapril Aurovitas” and “Warnings and precautions”).
• Other medicines to lower blood pressure, such as beta-blockers or diuretics (“water tablets”).
• Potassium supplements (including salt substitutes), potassium-sparing diuretics, and other medicines that may increase blood potassium levels (e.g., trimethoprim and cotrimoxazole for bacterial infections; cyclosporine, an immunosuppressant used to prevent organ transplant rejection; and heparin, a medicine used to thin the blood to prevent clots).
• Medicines for diabetes (including oral antidiabetic medicines and insulin).
• Lithium (a medicine used to treat certain types of depression).
• Medicines for depression called “tricyclic antidepressants”.
• Medicines for mental disorders called “antipsychotics”.
• Certain cough and cold medicines and weight-reducing medicines containing a substance called a “sympathomimetic agent”.
• Certain medicines for pain or arthritis, including gold therapy.
• An mTOR inhibitor (e.g., temsirolimus, sirolimus, everolimus: medicines used to treat certain cancers or to prevent organ transplant rejection). See also information under “Warnings and precautions”.
• A medicine containing a neprilysin inhibitor such as sacubitril (available in a fixed-dose combination with valsartan) or racecadotril. These may increase the risk of angioedema (swelling of the face, lips, tongue or throat with difficulty swallowing or breathing). See also information in sections “Do not take Enalapril Aurovitas” and “Warnings and precautions”.
• Non-steroidal anti-inflammatory drugs (NSAIDs), including COX-2 inhibitors (medicines that reduce inflammation and may help relieve pain).
• Aspirin (acetylsalicylic acid).
• Medicines used to dissolve blood clots (thrombolytics).
• Alcohol.

If you are unsure whether any of the above apply to you, consult your doctor or pharmacist before starting to take enalapril.

Taking Enalapril Aurovitas with food and drink

Enalapril can be taken with or without food. Most people take enalapril with a little water.

Pregnancy and breast-feeding

Pregnancy

If you are pregnant or breast-feeding, think you may be pregnant, or are planning to become pregnant, consult your doctor before using this medicine. Your doctor will usually advise you to stop taking enalapril before becoming pregnant or as soon as you know you are pregnant, and will recommend an alternative medicine. This medicine is not recommended during early pregnancy and must not be taken after the third month of pregnancy, as it may cause serious harm to your baby if used from the third month of pregnancy onwards.

Breast-feeding

Inform your doctor if you are breast-feeding or about to start breast-feeding. Breast-feeding is not recommended in newborns (first weeks after birth) and especially in premature infants while taking this medicine. For older infants, your doctor should advise you on the benefits and risks of taking this medicine compared to other treatments during breast-feeding.

Driving and using machines

You may feel dizzy or drowsy while taking this medicine. If this occurs, do not drive or operate tools or machinery.

Enalapril Aurovitas contains lactose

If your doctor has informed you that you have an intolerance to certain sugars, consult him before taking this medicine.

3. How to take Enalapril Aurovitas

Follow exactly the instructions for use of this medicine as given by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.

• It is very important that you continue taking this medicine for as long as your doctor has prescribed it.
• Do not take more tablets than prescribed.

High blood pressure

• The usual initial dose ranges between 5 mg and 20 mg, taken once daily.
• Some patients may require a lower initial dose.
• The usual long-term dose is 20 mg, taken once daily.
• The maximum long-term dose is 40 mg, taken once daily.

Heart failure

• The usual initial dose is 2.5 mg, taken once daily.
• Your doctor will gradually increase this dose until the appropriate dose for you is reached.
• The usual long-term dose is 20 mg per day, given in one or two divided doses.
• The maximum long-term dose is 40 mg per day, divided into two doses.

Patients with kidney problems

• Your medicine dose will change depending on how well your kidneys are functioning:
• Moderate kidney problems - 5 mg to 10 mg per day.
• Severe kidney problems - 2.5 mg per day.
• If undergoing dialysis - 2.5 mg per day. On days when you are not undergoing dialysis, your dose may change depending on how low your blood pressure is.

Elderly patients

Your doctor will decide the dose based on how well your kidneys are functioning.

Use in children

Experience with the use of enalapril in children with high blood pressure is limited. If the child can swallow tablets, the dose will be calculated according to the child's weight and blood pressure. The usual initial doses are:

• Between 20 kg and 50 kg - 2.5 mg per day.
• Over 50 kg - 5 mg per day.

The dose may be adjusted according to the child's needs:

• A maximum of 20 mg per day may be used in children weighing between 20 kg and 50 kg.
• A maximum of 40 mg per day may be used in children weighing over 50 kg.

This medicine is not recommended in newborn infants (first weeks after birth) or in children with kidney problems.

If you take more Enalapril Aurovitas than you should

If you take more enalapril than you should, consult your doctor or go to the hospital immediately. In case of overdose or accidental ingestion, call the Poison Information Service at telephone number 91 562 04 20. Take the medicine package with you. The following effects may occur: feeling dizzy or lightheaded. This is due to a sudden or excessive drop in blood pressure.

If you forget to take Enalapril Aurovitas

• If you forget to take a tablet, do not take the missed dose.
• Take your next dose as usual.
• Do not take a double dose to make up for forgotten doses.

If you stop taking Enalapril Aurovitas

Do not stop taking your medicine unless your doctor tells you to do so.

If you have any further questions about the use of this medicine, ask your doctor or pharmacist.

4. Possible adverse effects

Like all medicines, this medicine can cause adverse effects, although not everyone will experience them.

If you experience any of the following symptoms, stop taking enalapril and speak to your doctor immediately:

• Swelling of your face, lips, tongue or throat which may cause difficulty swallowing or breathing.
• Swelling of your hands, feet or ankles.
• If you develop a red rash on the skin with swelling (hives).

Please note that black patients have a higher risk of experiencing these types of reactions. If you experience any of the above reactions, stop taking enalapril and speak to your doctor immediately.

When you start taking this medicine, you may feel faint or dizzy. If this happens, lying down may help. This is due to a drop in your blood pressure. This will improve as you continue taking the medicine. If you are concerned, please speak to your doctor.

Other adverse effects include:

Very common (may affect more than 1 in 10 people)

• Feeling dizzy, weak or nauseous.
• Blurred vision.
• Cough.

Common (may affect up to 1 in 10 people)

• Dizziness due to low blood pressure, changes in heart rhythm, rapid heartbeat, angina or chest pain.
• Headache, depression, fainting (syncope), taste disturbances.
• Difficulty breathing.
• Diarrhea, abdominal pain.
• Tiredness (fatigue).
• Rash, allergic reactions with swelling of the face, lips, tongue or throat with difficulty swallowing or breathing.
• High levels of potassium in the blood, elevated creatinine levels in your blood (both are usually detected in a blood test).

Uncommon (may affect up to 1 in 100 people)

• Flushing.
• Sudden drop in blood pressure.
• Rapid or irregular heartbeat (palpitations).
• Myocardial infarction (possibly due to very low blood pressure in certain high-risk patients, including those with impaired blood flow to the heart or brain).
• Stroke (possibly due to very low blood pressure in high-risk patients).
• Anaemia (including aplastic and haemolytic anaemia).
• Confusion, drowsiness or inability to sleep, restlessness.
• Tingling or numbness sensation in your skin.
• Dizziness (vertigo).
• Ringing in the ears (tinnitus).
• Runny nose, sore throat or hoarseness.
• Asthma – associated with chest tightness.
• Slowed movement of food through your intestine (ileus), inflammation of the pancreas.
• Vomiting, indigestion, constipation, anorexia.
• Irritated stomach (gastric irritation), dry mouth, ulcer.
• Muscle cramps.
• Reduced kidney function, kidney failure.
• Increased sweating.
• Itching or hives.
• Hair loss.
• Malaise (general discomfort), high temperature (fever).
• Impotence.
• High levels of protein in your urine (detected in a test).
• Low blood sugar or sodium levels, elevated blood urea levels (all detected in a blood test).

Rare (may affect up to 1 in 1,000 people)

• “Raynaud's phenomenon” in which your hands and feet may become very cold and white due to poor blood flow.
• Changes in blood test values such as reduced numbers of white or red blood cells, reduced haemoglobin, reduced platelet count.
• Bone marrow depression.
• Swollen glands in the neck, armpits or groin.
• Autoimmune diseases.
• Sleep disturbances or difficulty sleeping.
• Fluid or other substance accumulation in the lungs (as seen on X-rays).
• Inflammation of the nose.
• Inflammation of the lungs causing difficulty breathing (pneumonitis).
• Inflammation of the cheeks, gums, tongue, lips, throat.
• Reduced amount of urine produced.
• Rash with target-like appearance (erythema multiforme).
• “Stevens-Johnson syndrome” and “toxic epidermal necrolysis” (a serious skin disorder in which you have red, peeling skin with blisters or open sores), exfoliative dermatitis/erythroderma (severe skin rash with peeling or shedding of the skin), pemphigus (small fluid-filled blisters on the skin).
• Liver or gallbladder problems such as reduced liver function, liver inflammation, jaundice (yellowing of the skin or eyes), elevated liver enzymes or bilirubin levels (detected in a blood test).
• Breast enlargement in men (gynaecomastia).

Very rare (may affect up to 1 in 10,000 people)

• Swelling in your intestine (intestinal angioedema).

Frequency not known (frequency cannot be estimated from available data)

• Excessive production of antidiuretic hormone, causing fluid retention, leading to weakness, tiredness or confusion.
• A group of symptoms has been reported which may include one or more of the following: fever, inflammation of blood vessels (serositis/vasculitis), muscle pain (myalgia/myositis), joint pain (arthralgia/arthritis). Skin rash, photosensitivity or other skin manifestations may occur.

Reporting of adverse effects

If you experience any adverse effects, talk to your doctor or pharmacist, even if they are possible adverse effects not listed in this leaflet. You may 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 Enalapril Aurovitas

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date stated on the blister and packaging after EXP. The expiry date refers to the last day of the month indicated.

Store below 30°C.

Medicines should not be disposed of via wastewater or household waste. Dispose of unused medicines and their containers at the SIGRE collection point at your pharmacy. If you have any doubts, ask your pharmacist how to properly dispose of medicines and containers you no longer need. This will help protect the environment.

6. Contents of the pack and other information

Composition of Enalapril Aurovitas

• The active substance is enalapril maleate. Each tablet contains 10 mg of enalapril maleate.
• The other components are: monohydrate lactose, pregelatinized corn starch and glycerol distearate (Type I).

Appearance of the medicine and contents of the pack

Uncoated tablets, white to off-white, round (6.5 mm in diameter), with flat faces and bevelled edges, marked "10" on one side and scored on the other side. The tablet can be divided into equal doses.

Enalapril Aurovitas is available in triple-layer cold-form aluminum blisters (Alu-Alu) and transparent PVC – aluminum foil laminates.

Pack sizes: 28, 30, 50, 56, 90 & 100 tablets.

Only some pack sizes may be marketed.

Marketing Authorization Holder and Manufacturer

Marketing Authorization Holder:

Aurovitas Spain, S.A.U.

Avda. de Burgos, 16-D

28036 Madrid

Spain

Manufacturer:

APL Swift Services (Malta) Limited

HF26, Hal Far Industrial Estate, Hal Far

Birzebbugia, BBG 3000

Malta

Or

Generis Farmacêutica, S.A.

Rua João de Deus, 19

2700-487 Amadora

Portugal

This medicinal product is authorized in the European Economic Area member states under the following names:

Spain: Enalapril Aurovitas 10 mg tablets

Italy: Enalapril Aurobindo Pharma Italia

Netherlands: Enalaprilmaleaat Aurobindo 10 mg, tabletten

Portugal: Enalapril Generis

Date of the most recent revision of this leaflet: March 2026

Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es)