If you develop dizziness, weakness, or drowsiness during treatment with this medicine, you should not drive vehicles or operate machines.
Enalapril/Lercanidipine ratiopharm contains sodium
This medicine contains less than 1 mmolof sodium (23 mg) per coated tablet; this is, essentially “sodium-free”.
Follow exactly the administration instructions for this medication as indicated by your doctor. In case of doubt, consult your doctor or pharmacist again.
Adults: unless otherwise indicated by your doctor, the recommended dose is one tablet once a day at the same time every day. Tablets should preferably be taken in the morning at least 15 minutes before breakfast. Tablets should be swallowed whole with water. See “Taking Enalapril/Lercanidipino ratiopharm with food, drinks, and alcohol”.
Patients with kidney problems/advanced age:Your doctor will decide the medication dose you should take, taking into account how well your kidneys are functioning.
If you take more Enalapril/Lercanidipino ratiopharm than you should
Do not exceed the prescribed dose. If you have taken more tablets than the prescribed dose, consult your doctor immediately or go to the hospital immediately. Bring the packaging with you.
A dose higher than the correct one may cause excessive blood pressure drop and your heart may beat irregularly or faster.
In case of overdose or accidental ingestion, call the Toxicological Information Service, phone 91 562 04 20.
If you forgot to take Enalapril/Lercanidipino ratiopharm
If you interrupt treatment with Enalapril/Lercanidipino ratiopharm
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medicines, Enalapril/ Lercanidipino ratiopharm can cause side effects, although not everyone will experience them..This medicine may cause the following side effects:
Some side effects may be serious.
Inform your doctor immediately if you notice any of the following side effects:
When you start taking Enalapril/ Lercanidipino ratiopharm, you may feel weakness or dizziness, or notice that your vision becomes blurry; this is caused by a sudden drop in blood pressure, and if it happens, it will be helpful to lie down. If you are concerned, consult your doctor.
Side effects observed with Enalapril/ Lercanidipino ratiopharm
Frequent(may affect up to 1 in 10 people)
Cough, sensation of dizziness, headache
Infrequent(may affect up to 1 in 100 people)
Changes in blood parameters, such as a decrease in platelet count, an increase in potassium levels in the blood, nervousness (anxiety), sensation of dizziness when standing up, vertigo, rapid or irregular heartbeat (palpitations), sudden redness of the face, neck, or upper chest (erythema), low blood pressure, abdominal pain, constipation, feeling sick (nausea), increase in liver enzyme levels, skin redness, joint pain, increased urination frequency, feeling weak, fatigue, sensation of heat, inflammation of the ankles.
Rare(may affect up to 1 in 1,000 people)
Anemia, allergic reactions, ringing in the ears (tinnitus), fainting, dry throat, sore throat, indigestion, salty sensation in the tongue, diarrhea, dry mouth, gum inflammation, allergic reaction with swelling of the face, lips, tongue, or throat that causes difficulty breathing or swallowing, skin rash, urticaria, nocturia, polyuria, impotence.
Additional side effects observed with enalapril or lercanidipine alone
Enalapril
Very frequent(may affect more than 1 in 10 people)
Blurred vision, feeling dizzy, weak, or sick, and coughing
Frequent(may affect less than 1 in 10 people)
Depression, headache, fainting (syncope), chest pain, sensation of dizziness due to low blood pressure, changes in heart rate, rapid heartbeat, angina, shortness of breath, alterations in taste, increased creatinine levels in the blood (usually detected through a blood test), high potassium levels in the blood, diarrhea, abdominal pain, fatigue (fatigue), rash, allergic reaction with swelling of the face, lips, tongue, or throat that causes difficulty breathing or swallowing.
Infrequent(may affect up to 1 in 100 people)
Anemia (including aplastic and hemolytic anemia), sudden drop in blood pressure, confusion, nervousness, somnolence or insomnia, sensation of pinpricks in the skin or numbness, myocardial infarction (possibly caused by very low blood pressure in certain high-risk patients, including those with heart or brain blood supply problems), stroke (possibly due to very low blood pressure in high-risk patients), nasal congestion, sore throat, and hoarseness, asthma-like oppression in the chest, slowed movement of food through the intestines (ileus), pancreatitis, feeling sick (vomiting), indigestion, constipation, stomach irritation (gastritis), dry mouth, ulcer, anorexia, itching or urticaria, hair loss, renal function alteration, renal insufficiency, increased sweating, high protein levels in the urine (measured through a blood test), muscle cramps, general feeling of discomfort, high temperature (fever), low sugar or sodium levels in the blood, high urea levels in the blood (all measured through a blood test), redness, rapid or irregular heartbeat (palpitations), vertigo (sensation of spinning), tinnitus, impotence.
Rare(may affect up to 1 in 1,000 people)
Changes in blood parameters, such as a decrease in white blood cell count, bone marrow depression, autoimmune diseases, strange dreams or sleep disorders, Raynaud's phenomenon (in which hands and feet may become intensely cold and acquire a white color due to low blood flow), pulmonary infiltrates, nasal inflammation, pneumonia, liver problems, such as decreased liver function, liver inflammation, jaundice (yellowing of the skin or eyes), increased liver enzyme levels or bilirubin (measured through a blood test), erythema multiforme (red spots of different shapes that appear on the skin), Stevens-Johnson syndrome and toxic epidermal necrolysis (a severe skin condition characterized by redness of the skin and the formation of scales, blisters, or open sores), dermatitis exfoliativa/erythrodermia (severe skin rash with peeling or shedding of the skin), or pemphigus (small fluid-filled blisters on the skin), decreased urine production, gynecomastia (breast enlargement in men), inflammation of the glands in the neck, armpits, or groin, accumulation of fluid or other substances in the lungs (as seen on X-rays), inflammation of the cheeks, gums, tongue, lips, and throat.
Very rare(may affect up to 1 in 10,000 people)
Intestinal angioedema (inflammation of the intestines)
Frequency unknown(the frequency cannot be estimated from available data)
Excessive production of antidiuretic hormone, leading to fluid retention, resulting in weakness, fatigue, or confusion.
A complex of symptoms that may include one or more of the following symptoms: fever, inflammation of blood vessels (serositis/vasculitis), muscle pain (myalgia, myositis), joint pain (arthralgia/arthritis). It may also cause a rash, photosensitivity, and other skin manifestations.
Lercanidipine
Some side effects may be serious.
Inform your doctor immediately if any of the following occur:
Rare(may affect up to 1 in 1,000 people)
Angina pectoris (chest pain caused by lack of blood supply to the heart) allergic reactions (symptoms include itching, rash, urticaria), fainting.
Patients with pre-existing angina pectoris may experience an increase in frequency, duration, or severity of attacks associated with treatment with the group of medications to which lercanidipine belongs. Isolated cases of myocardial infarction have been observed.
Other possible side effects:
Frequent(may affect up to 1 in 10 people):
Headache, rapid heart rate, rapid or irregular heartbeat (palpitations), sudden redness of the face, neck, or upper chest (erythema), swelling of the ankles.
Infrequent(may affect up to 1 in 100 people):
Dizziness, low blood pressure, acid reflux, nausea, stomach pain, skin rash, itching, muscle pain, polyuria, feeling weak or tired.
Rare(may affect up to 1 in 1,000 people):
Somnolence, vomiting, diarrhea, urticaria, increased frequency of urination, chest pain.
Frequency unknown(the frequency cannot be estimated from available data):
Gum inflammation, changes in liver function (detected through blood tests), cloudy fluids (when dialysis is performed through a tube in your abdomen), inflammation of the face, tongue, or throat that may cause difficulty breathing or swallowing.
If any side effects worsen or if you experience any type of side effect not listed in this prospectus, inform your doctor or pharmacist. You can consult your doctor or pharmacist for more information about side effects, as both have a more comprehensive list of side effects.
Reporting side effects
If you experience any type of side effects,consult your doctor or pharmacist, eveniftheyare not listed in this prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use: https://www.notificaram.es.By reporting side effects, you can contribute to providing more information about the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the blister pack and on the packaging after “CAD”. The expiration date is the last day of the month indicated.
Do not store at a temperature above 25°C.
Medications should not be disposed of through drains or in the trash. Dispose of the packaging and medications you no longer need at the SIGRE point of the pharmacy.
In case of doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
The active substances are enalapril maleate and lercanidipine hydrochloride.
Each tablet contains: 20 mg of enalapril maleate and 10 mg of lercanidipine hydrochloride.
The other components are:
Core: microcrystalline cellulose, sodium hydrogen carbonate, pregelatinized cornstarch, sodium carboxymethylstarch (type IA), anhydrous colloidal silica, magnesium stearate.
Coating: hypromellose, macrogol 6000, talc, titanium dioxide (E171), iron oxide yellow (E172).
Appearance of the product and contents of the packaging
Enalapril/ Lercanidipine ratiopharm 20 mg/10 mg tablets areround, biconvex, yellowish film-coated tablets.
Enalapril/ Lercanidipine ratiopharm 20 mg/10 mg is available in packs of 14, 28, 30, 50, 56 and 100 tablets.
Only some pack sizes may be marketed.
Marketing authorization holder and responsible manufacturer
Marketing authorization holder
Teva Pharma, S.L.U.
c/ Anabel Segura 11, Edificio Albatros B 1st floor
Alcobendas, 28108 Madrid (Spain)
Responsible manufacturer
TEVA Gyógyszergyár Zrt.
Pallagi street 13, Debrecen H-4042
Hungary
or
Teva Pharma S.L.U.
C/ C, nº 4, Industrial Estate Malpica
Zaragoza 50016
or
Merckle GmbH
Ludwig- Merckle Street 3
Blaubeuren 89143
Germany
This medicinal product is authorized in the Member States of the European Economic Area with the following names:
Austria: Enalapril/Lercanidipin ratiopharm 20 mg/10 mg Filmtabletten
Spain: Enalapril/ Lercanidipine ratiopharm 20 mg/10 mg film-coated tablets
Portugal: Enalapril + Lercanidipine ratiopharm
Last review date of this leaflet: July 2024
Detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) www.aemps.gob.es
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