


Ask a doctor about a prescription for ENALAPRIL STADA 20 mg TABLETS
Package Leaflet: Information for the User
Enalapril STADA 20 mg Tablets EFG
Enalapril Maleate
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Enalapril Stada belongs to a group of medicines called angiotensin-converting enzyme inhibitors (ACE inhibitors).
Enalapril Stada is indicated for:
Do not take Enalapril Stada:
Warnings and precautions
Consult your doctor or pharmacist before starting to take Enalapril Stada.
Your doctor may monitor your kidney function, blood pressure, and blood electrolyte levels (e.g., potassium) at regular intervals.
See also the information under the heading "Do not take Enalapril Stada".
You must inform your doctor if you think you are pregnant (or might be). Enalapril is not recommended at the beginning of 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 during this period (see section Pregnancy).
Keep in mind that enalapril lowers blood pressure in black patients less effectively than in non-black patients.
In all these cases, inform your doctor, as you may need a dose adjustment or discontinuation of enalapril or monitoring of your potassium blood levels. If you have diabetes and are taking oral antidiabetics or insulin, you should closely monitor your blood glucose levels, especially during the first month of treatment with enalapril.
Before undergoing surgery or anesthesia (even at the dentist), inform your doctor or dentist that you are taking enalapril, as there may be a sudden drop in blood pressure associated with anesthesia.
Other medicines and Enalapril Stada
Inform your doctor or pharmacist if you are using, have recently used, or might use any other medicines.
Certain medicines may interact with enalapril; in these cases, your doctor may need to adjust your dose and/or take other precautions.
It is important that you inform your doctor if you are taking or have recently taken any of the following medicines:
This applies especially if you are also taking:
Taking Enalapril Stada with food, drinks, and alcohol
Food does not affect the absorption of enalapril.
Alcohol enhances the blood-pressure-lowering effect of enalapril; therefore, inform your doctor if you are taking alcoholic beverages while being treated with this medicine.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Pregnancy
You must inform your doctor if you think you are pregnant (or might be). Normally, your doctor will advise you to stop taking enalapril before you become pregnant or as soon as you know you are pregnant and will advise you to take a different medicine instead of enalapril. Enalapril is not recommended at the beginning of 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 during this period.
Breastfeeding
Inform your doctor if you are breastfeeding or about to start breastfeeding. While taking enalapril, breastfeeding is not recommended in newborns (first few weeks after birth), and especially in premature babies. In the case of an older baby, your doctor should advise you on the benefits and risks of taking enalapril, compared to other treatments, while breastfeeding.
Driving and using machines
Individual responses to the medicine may vary.
Since enalapril can cause dizziness or fatigue, do not perform tasks that require special attention (driving vehicles or operating machinery) until you know how the medicine affects you.
Enalapril Stada contains lactose and sodium
If your doctor has told you that you have an intolerance to some sugars, consult him before taking this medicine.
This medicine contains less than 23 mg of sodium (1 mmol) per tablet; this is essentially "sodium-free".
Take this medicine exactly as your doctor or pharmacist has told you. If you are not sure, ask your doctor or pharmacist.
Your doctor will decide the duration of your treatment with enalapril. Do not stop treatment before this.
Enalapril Stada can be taken with or without food, with a glass of water.
Your doctor will decide the appropriate dose of enalapril for you, depending on your condition and whether you are taking other medicines.
Hypertension
For most patients, the initial recommended dose is 5 to 20 mg once daily. Some patients may need a lower initial dose.
The usual long-term dose is 20 mg once daily.
Heart Failure
The initial recommended dose is 2.5 mg once daily. Your doctor will gradually increase the dose until the appropriate dose for you is reached. The usual long-term dose is 20 mg daily in one or two divided doses.
At the start of treatment, precautions should be taken due to the possibility of dizziness or lightheadedness.
Inform your doctor immediately if you experience these symptoms.
If you think the effect of enalapril is too strong or too weak, tell your doctor or pharmacist.
If you take more Enalapril Stada than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately, or call the Toxicology Information Service, telephone: 91 562 04 20, indicating the medicine and the amount taken. It is recommended to take the package and the leaflet of the medicine to the healthcare professional.
In case of an overdose, the most likely symptom is a feeling of dizziness or lightheadedness due to a sudden or excessive drop in blood pressure.
If you forget to take Enalapril Stada
Continue taking enalapril as prescribed by your doctor. Do not take a double dose to make up for forgotten doses.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.
The adverse reactions reported for enalapril are detailed below:
Frequencies are defined as: very frequent (affecting more than 1 in 10 people); frequent (affecting between 1 and 10 in 100 people); uncommon (affecting between 1 and 10 in 1,000 people); rare (affecting between 1 and 10 in 10,000 people); very rare (affecting less than 1 in 10,000 people).
Blood and Lymphatic System Disorders
Uncommon: anemia (including aplastic and hemolytic anemia).
Rare: blood disorders, such as abnormally low neutrophil count, low hemoglobin levels, reduction or complete absence of granulocytes, deficiency of all cellular elements in the blood, bone marrow depression, lymph node disease or abnormal immune response.
Metabolic and Nutritional Disorders
Uncommon: low blood sugar levels (hypoglycemia).
Nervous System and Mental Disorders
Frequent: headache, depression.
Uncommon: confusion, somnolence or inability to sleep, nervousness, sensation of tingling or numbness, vertigo.
Rare: sleep disturbances, sleep problems.
Eye Disorders
Very frequent: blurred vision.
Cardiac and Vascular Disorders
Very frequent: dizziness.
Frequent: drop in blood pressure (including orthostatic hypotension), fainting, chest pain, cardiac rhythm disturbances, angina pectoris, rapid heartbeat.
Uncommon: orthostatic hypotension (decrease in blood pressure when sitting or standing), rapid and strong heartbeat, myocardial infarction or stroke possibly due to excessively low blood pressure in high-risk patients (patients with alterations in heart and/or brain blood flow).
Rare: small arteries, usually in the fingers or toes, that produce spasms that make the skin turn pale or a reddish-blue color (Raynaud's phenomenon).
Respiratory, Thoracic, and Mediastinal Disorders
Very frequent: cough.
Frequent: difficulty breathing.
Uncommon: nasal mucous discharge, throat itching and hoarseness, asthma.
Rare: fluid in the lungs, inflammation of the nasal mucosa, allergic inflammation of the lungs.
Gastrointestinal Disorders
Very frequent: nausea.
Frequent: diarrhea, abdominal pain, alteration of taste.
Uncommon: intestinal obstruction, pancreatitis, vomiting, indigestion, constipation, anorexia, gastric irritation, dry mouth, peptic ulcer.
Rare: mouth inflammation and ulcers, tongue inflammation.
Very rare: intestinal angioedema (intestinal swelling)
Hepatobiliary Disorders
Rare: liver failure, liver inflammation (hepatitis), reduction or obstruction of bile flow from the bile duct to the liver (cholestasis including jaundice).
Skin and Subcutaneous Tissue Disorders
Frequent: skin rash, hypersensitivity or allergic reaction that causes swelling of the face, limbs, lips, tongue, glottis, and larynx.
Uncommon: sweating, pruritus (itching sensation), urticaria (red and itchy swelling), hair loss.
Rare: severe skin reaction, including excessive redness of the skin, blisters, skin peeling.
A symptomatic complex has been observed that may include some of the following reactions: fever, blood vessel inflammation, pain and inflammation of muscles and joints, blood disorders that affect blood components and are usually detected in a blood test, skin rash, hypersensitivity to sunlight and other skin effects.
Renal and Urinary Disorders
Uncommon: reduced renal function or renal failure, presence of proteins in the urine. Rare: reduction in the amount of urine produced per day.
Reproductive System and Breast Disorders
Uncommon: impotence.
Rare: breast enlargement in men.
General Disorders and Administration Site Conditions
Very frequent: weakness.
Frequent: fatigue.
Uncommon: muscle cramps, flushing, ringing in the ears, general malaise, fever.
Clinical Laboratory Tests
Frequent: high potassium levels in blood, increased creatinine levels in blood.
Uncommon: increased urea levels in blood, decreased sodium levels in blood.
Rare: increased liver enzymes, increased bilirubin levels in blood.
Stop taking Enalapril STADA and consult your doctor immediately in any of the following cases:
You should be aware that black patients are more sensitive to this type of adverse reactions. If you observe any other reaction not described in this leaflet, consult your doctor or pharmacist.
Adverse Reaction Reporting
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect that does not appear in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines. https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of sight and reach of children.
This medicine does not require special storage conditions.
Do not use this medicine after the expiration date that appears on the packaging, after CAD. The expiration date is the last day of the month indicated.
Medicines should not be thrown down the drain or into the trash. Deposit the packaging and medicines you no longer need at the SIGRE point in the pharmacy. Ask your pharmacist how to dispose of the packaging and medicines you no longer need. This will help protect the environment.
Composition of Enalapril Stada
Appearance of the Product and Package Contents
Enalapril Stada 20 mg is presented in the form of pink, round, flat tablets with a score on one side and the inscription "20" on the other.
The score serves only to facilitate fractionation and swallowing, but not to divide into equal doses.
Each package contains 28 or 500 (clinical package) tablets
Only some package sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Laboratory STADA, S.L.
Frederic Mompou, 5
08960 Sant Just Desvern (Barcelona)
Spain
Manufacturer
Neuraxpharm Pharmaceuticals, S.L.
Avda. Barcelona, 69
08970 Sant Joan Despí (Barcelona)
Spain
Date of the Last Revision of this Leaflet: November 2019
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es
The average price of ENALAPRIL STADA 20 mg TABLETS in November, 2025 is around 1.61 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.
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