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Enalapril Vitabalans

Enalapril Vitabalans

About the medicine

How to use Enalapril Vitabalans

Leaflet accompanying the packaging: information for the user

Enalapril Vitabalans, 5 mg, tablets

Enalapril Vitabalans, 10 mg, tablets

Enalapril Vitabalans, 20 mg, tablets

Enalapril maleate

You should carefully read the contents of the leaflet before taking the medicine, as it contains important information for the patient.

  • You should keep this leaflet, so that you can read it again if necessary.
  • In case of any doubts, you should consult a doctor or pharmacist.
  • This medicine has been prescribed specifically for you. Do not pass it on to others. The medicine may harm another person, even if their symptoms are the same.
  • If the patient experiences any side effects, including any side effects not listed in this leaflet, they should tell their doctor or pharmacist. See section 4.

Table of contents of the leaflet:

  • 1. What is Enalapril Vitabalans and what is it used for
  • 2. Important information before taking Enalapril Vitabalans
  • 3. How to take Enalapril Vitabalans
  • 4. Possible side effects
  • 5. How to store Enalapril Vitabalans
  • 6. Contents of the packaging and other information

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

Enalapril Vitabalans belongs to a group of medicines called ACE inhibitors. This medicine works by widening the blood vessels, making it easier for the heart to pump blood through the vessels to all parts of the body. This leads to a decrease in high blood pressure.

Enalapril Vitabalans is used:

  • to treat high blood pressure (hypertension)
  • to treat symptomatic heart failure (a condition in which the heart is not able to pump enough blood to meet the body's needs)
  • to prevent symptomatic heart failure in patients whose heart function is impaired but who do not yet have symptoms of the disease

2. Important information before taking Enalapril Vitabalans

When not to take Enalapril Vitabalans

  • if the patient is allergic to enalapril maleate or any of the other ingredients of this medicine (listed in section 6)
  • in case of previous allergic reactions caused by taking an ACE inhibitor, known as angioedema, which is characterized by swelling of the skin of the hands, feet, face, or swelling of the lips, tongue, or throat, causing difficulty swallowing or breathing
  • if the patient has previously experienced angioedema of unknown cause or if there is a history of angioedema in a close relative - the tendency to such a reaction may be familial
  • if the patient has taken or is currently taking sacubitril/valsartan, a medicine used to treat a certain type of long-term (chronic) heart failure in adults, as it increases the risk of angioedema

after the third month of pregnancy (it is also recommended to avoid taking Enalapril Vitabalans in early pregnancy - see "Pregnancy")

  • if the patient has diabetes or kidney problems and is being treated with a blood pressure-lowering medicine containing aliskiren

Warnings and precautions

Before starting to take Enalapril Vitabalans, the patient should discuss it with their doctor or pharmacist.

  • in case of prolonged and severe diarrhea and vomiting
  • if the patient is taking medicines that increase urine production, i.e., diuretics
  • if the patient is on a low-salt diet
  • if the patient has other heart and blood vessel diseases, such as coronary artery disease (angina pectoris), cerebrovascular disorders, heart valve disorders, aortic stenosis, or a heart muscle disease called cardiomyopathy
  • in case of kidney function disorders requiring hemodialysis or after a kidney transplant
  • in case of narrowing of the renal artery causing high blood pressure
  • if the patient has liver function disorders
  • in case of connective tissue diseases that affect blood vessels, such as Raynaud's disease or systemic sclerosis
  • if the patient has previously experienced a prolonged, dry cough while taking ACE inhibitors (see section 4 "Possible side effects")
  • if the patient has been desensitized, for example, to bee or wasp venom
  • in case of LDL apheresis treatment for diabetes (see section 2 "Taking other medicines")
  • in patients with collagen vascular disease, taking immunosuppressive medicines (used to treat autoimmune disorders such as rheumatoid arthritis or after organ transplantation), allopurinol (used to treat gout), or procainamide (used to treat heart rhythm disorders). The doctor may periodically take a blood sample to check the white blood cell count. If such patients experience symptoms of infection (e.g., elevated temperature, fever), they should immediately inform their doctor
  • in case of taking potassium supplements or potassium-sparing diuretics
  • in case of taking lithium, used to treat certain mental disorders
  • in black patients, as the effect of enalapril may be weaker
  • if the patient is taking any of the following medicines used to treat high blood pressure:
  • angiotensin II receptor antagonist (ARB) (also known as sartans - e.g., valsartan, telmisartan, irbesartan), especially if the patient has kidney problems related to diabetes
  • aliskiren. The doctor may monitor kidney function, blood pressure, and electrolyte levels (e.g., potassium) in the blood at regular intervals. See also the information under the heading "When not to take Enalapril Vitabalans" and "Warnings and precautions"

If the patient is taking any of the following medicines, the risk of angioedema may increase:

  • racecadotril, a medicine used to treat diarrhea
  • medicines used to prevent organ rejection and to treat cancer (e.g., temsirolimus, sirolimus, everolimus)
  • vildagliptin, a medicine used to treat diabetes

During treatment with Enalapril Vitabalans, the patient should immediately inform their doctor if they experience any of the following symptoms:

  • dizziness after taking the first dose. Some people may react to the first dose or an increase in dose with dizziness, weakness, fainting, and/or vomiting
  • sudden swelling of the lips and face, tongue, larynx, throat, and sometimes hands and feet, or a wheezing breath or hoarseness. This condition is called angioedema. It can occur at any time during treatment. ACE inhibitors more frequently cause angioedema in black patients than in other races
  • high fever, sore throat, or mouth ulcers (these may be symptoms of an infection caused by a low white blood cell count)
  • yellowing of the skin and whites of the eyes (jaundice), which can be symptoms of liver disease

If any of the above situations apply to the patient, they should consult their doctor before starting treatment with Enalapril Vitabalans tablets.

In case of planned surgery or operation under general or spinal anesthesia, the patient should inform the anesthesiologist about taking Enalapril Vitabalans.

The patient should inform their doctor if they are pregnant or planning to become pregnant. It is not recommended to take Enalapril Vitabalans in early pregnancy and it should not be taken after the third month of pregnancy, as it may seriously harm the baby (see "Pregnancy").

Enalapril Vitabalans and other medicines

The patient should tell their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.

In particular, the doctor should be informed about the use of the following medicines:

  • diuretics
  • potassium supplements (including salt substitutes), potassium-sparing diuretics, and other medicines that increase potassium levels in the blood (e.g., trimethoprim and co-trimoxazole, used to treat bacterial infections; cyclosporine, an immunosuppressive medicine used to prevent organ rejection; heparin, a medicine used to thin the blood to prevent clots)
  • other medicines used to treat high blood pressure
  • other medicines that may lower blood pressure, such as nitrates used to treat angina, tricyclic antidepressants, medicines used to treat mental disorders (phenothiazines), or barbiturates used to treat epilepsy, narcotic analgesics, and anesthetics
  • lithium (used to treat manic-depressive disorders)
  • oral antidiabetic medicines (both insulin and oral antidiabetic medicines) - the dosage of these medicines may need to be adjusted
  • allopurinol (used to treat gout) or procainamide (used to treat heart rhythm disorders)
  • immunosuppressive medicines, used, for example, after organ transplantation
  • non-steroidal anti-inflammatory medicines (NSAIDs), such as acetylsalicylic acid, ibuprofen, or ketoprofen, used regularly or for a long time - Note: While taking Enalapril Vitabalans tablets, it is safe to use small doses of acetylsalicylic acid (e.g., 50 mg or 100 mg per day) to prevent clots
  • sympathomimetic medicines
  • concomitant treatment with gold preparations may cause facial flushing, nausea, vomiting, and a decrease in blood pressure

The doctor may need to adjust the dose and/or take other precautions:

If the patient is taking an angiotensin II receptor antagonist (ARB) or aliskiren (see also the information under the heading "When not to take Enalapril Vitabalans" and "Warnings and precautions").

Enalapril Vitabalans with food and drink

Meals and drinks do not affect the absorption of enalapril. The tablets can be taken on an empty stomach or with a meal with a sufficient amount of liquid, for example, with a glass of water.

Consuming a large amount of salt (sodium chloride) may weaken the effect of Enalapril Vitabalans.

Consuming foods containing a large amount of potassium and salt substitutes while taking Enalapril Vitabalans is not recommended, as potassium levels in the blood may increase excessively.

Alcohol may enhance the effect of Enalapril Vitabalans on blood pressure.

Pregnancy and breastfeeding

Pregnancy

If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a baby, they should consult their doctor or pharmacist before taking this medicine. The doctor will usually recommend stopping Enalapril Vitabalans before planned pregnancy or as soon as pregnancy is confirmed and recommend taking another medicine instead of Enalapril Vitabalans. It is not recommended to take Enalapril Vitabalans in early pregnancy and it should not be taken after the third month of pregnancy, as it may seriously harm the baby.

Breastfeeding

The patient should inform their doctor about breastfeeding or intending to breastfeed. It is not recommended to breastfeed newborns (the first few weeks after birth), especially premature babies, while taking Enalapril Vitabalans.

In the case of older infants, the doctor will inform about the benefits and risks of taking Enalapril Vitabalans during breastfeeding, compared to other treatment options.

Driving and using machines

While driving vehicles or operating machines, it should be taken into account that dizziness or fatigue may occur.

Enalapril Vitabalans may cause side effects related to low blood pressure, such as dizziness, fainting, or blurred vision (see section 4 "Possible side effects"). These usually occur at the beginning of treatment or after a dose increase; their occurrence is unlikely during long-term treatment. If such symptoms occur, the patient should avoid driving vehicles or performing other tasks that require concentration.

3. How to take Enalapril Vitabalans

This medicine should always be taken as directed by the doctor. In case of doubts, the patient should consult their doctor or pharmacist.

Enalapril Vitabalans can be taken with or between meals, with a sufficient amount of liquid, for example, with a glass of water.

Adults:

Treatment of high blood pressure:

The initial dose is usually 5 mg to 20 mg once a day, and the maintenance dose is 20 mg once a day.

Treatment of heart failure:

The initial dose is 2.5 mg per day. The dose should be gradually increased until the maintenance dose is reached. The maintenance dose is usually 20 mg per day, given in one dose or in two divided doses.

Elderly patients and patients with renal impairment:

The dose should be adjusted according to the patient's renal function.

Use in children

The appropriate dose is determined based on the child's body weight.

If the patient thinks that the effect of Enalapril Vitabalans is too strong or too weak, they should inform their doctor.

Taking a higher dose of Enalapril Vitabalans than recommended

In case of taking too much of the medicine, the patient should immediately contact their doctor, emergency department, or the nearest hospital. The most common signs and symptoms of overdose are low blood pressure and drowsiness (a state of almost complete loss of consciousness). Other symptoms include dizziness or lightheadedness caused by low blood pressure, rapid heartbeat, anxiety, cough, kidney failure, and rapid breathing.

Missing a dose of Enalapril Vitabalans

The patient should not take a double (or increased) dose to make up for missed doses. They should take the next tablet at the usual time.

Stopping treatment with Enalapril Vitabalans

If treatment is stopped, blood pressure may increase. If blood pressure is too high, it can affect heart and kidney function. The patient should not stop taking the medicine unless their doctor recommends it.

In case of any further doubts about taking this medicine, the patient should consult their doctor or pharmacist.

4. Possible side effects

Like all medicines, Enalapril Vitabalans can cause side effects, although not everybody gets them.

Very common (occurring in more than 1 in 10 patients):

  • visual disturbances
  • dizziness, weakness
  • dry cough (the patient should contact their doctor if a persistent cough occurs while taking Enalapril Vitabalans)
  • nausea

Common (occurring in 1 to 10 patients in 100):

  • headache, depression, fatigue
  • excessive lowering of blood pressure or lowering of blood pressure when standing up (which can cause dizziness or fainting)
  • chest pain, heart rhythm disorders, rapid heartbeat (tachycardia)
  • shortness of breath
  • diarrhea, abdominal pain, taste disturbances
  • rash and other hypersensitivity reactions (see below "Angioedema")
  • increased potassium and creatinine levels in the blood

Uncommon (occurring in 1 to 10 patients in 1,000):

  • anemia
  • excessive lowering of blood sugar (hypoglycemia) in patients with diabetes
  • confusion, nervousness, sensory disturbances, such as tingling or numbness (paresthesia), dizziness, drowsiness, insomnia
  • feeling of strong heartbeat (palpitations)
  • runny nose, sore throat, hoarseness, shortness of breath
  • ringing in the ears
  • dry mouth, vomiting, heartburn, stomach upset, constipation, weight loss
  • stomach or duodenal ulcer, intestinal obstruction, pancreatitis (which can cause abdominal pain)
  • excessive sweating, itching, hives, hair loss, flushing
  • kidney function impairment, protein in the urine
  • impotence
  • muscle cramps, general malaise, fever (see below "Fever of unknown origin")

Rare (occurring in 1 to 10 patients in 10,000):

  • low white blood cell count (see below "Fever of unknown origin")
  • low platelet count (which can cause nosebleeds and a tendency to bruise)
  • enlarged lymph nodes, development of an autoimmune disease
  • nightmares, sleep disturbances
  • worsening of Raynaud's syndrome (pain in the fingers and toes, which initially turn white, then blue, and finally red)
  • pulmonary infiltrates, allergic alveolitis, eosinophilic pneumonia
  • mouth ulcers, aphthous ulcers in the mouth, tongue inflammation
  • liver function impairment, hepatitis, bile duct obstruction with jaundice (yellowing of the skin and whites of the eyes)
  • severe blistering or exfoliative skin and mucous membrane disorders (erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, pemphigus, lupus erythematosus)
  • a syndrome involving fever, muscle or blood vessel inflammation, muscle and joint pain (see below "Fever of unknown origin")
  • decreased urine output
  • breast enlargement (in men)
  • increased liver enzyme activity, increased bilirubin levels in the blood
  • Very rare (occurring in less than 1 in 10,000 patients):

    • intestinal angioedema (intestinal edema)

    Frequency not known (cannot be estimated from the available data):

    • syndrome of inappropriate antidiuretic hormone secretion

    Angioedema

    The patient should immediately contact their doctor if they experience any of the following symptoms while taking Enalapril Vitabalans: swelling of the hands, feet, face, or swelling of the tongue or throat, which can cause difficulty swallowing or breathing

    Fever of unknown origin

    The patient should immediately contact their doctor if they experience a fever of unknown origin with accompanying symptoms such as a sore throat while taking Enalapril Vitabalans.

    Reporting side effects

    If the patient experiences any side effects, including any side effects not listed in the leaflet, they should tell their doctor or pharmacist. Side effects can be reported directly to the Department of Medicines Monitoring, Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych, Al. Jerozolimskie 181C, 02-222 Warsaw, Tel.: +48 22 49 21 301, Fax: +48 22 49 21 309, e-mail: ndl@urpl.gov.pl. By reporting side effects, more information can be collected on the safety of the medicine.

    5. How to store Enalapril Vitabalans

    The medicine should be stored out of sight and reach of children.

    Store in a temperature below 25°C.

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

    Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.

    6. Contents of the packaging and other information

    What Enalapril Vitabalans contains

    The active substance is enalapril maleate. Each tablet contains 5 mg, 10 mg, or 20 mg of enalapril maleate.

    Other ingredients: maize starch, microcrystalline cellulose, calcium hydrogen phosphate dihydrate, povidone K-29/32, sodium hydrogen carbonate, magnesium stearate, talc.

    Enalapril Vitabalans 10 mg tablets also contain a coloring agent (iron oxide red, E172).

    Enalapril Vitabalans 20 mg tablets also contain a coloring agent (iron oxide red and iron oxide yellow, E172).

    What Enalapril Vitabalans looks like and contents of the pack

    What Enalapril Vitabalans looks like

    Enalapril Vitabalans 5 mg: The tablets are white, round, flat, with a notch on one side of the tablet. The diameter is 8 mm.

    Enalapril Vitabalans 10 mg: The tablets are reddish-brown, round, flat, with a notch on one side of the tablet. The diameter is 8 mm.

    Enalapril Vitabalans 20 mg: The tablets are light orange, round, flat, with a notch on one side of the tablet. The diameter is 8 mm.

    The tablet can be divided into equal doses.

    Package sizes: 28, 30, 56, 60, 98, 100 tablets.

    Not all pack sizes may be marketed.

    Marketing authorization holder and manufacturer

    Vitabalans Oy, Varastokatu 8, 13500 Hämeenlinna, Finland, Tel: +358 (3) 615600, Telefax: +358 (3) 6183130

    This medicinal product is authorized in the Member States of the European Economic Area under the following names

    Enalapril Vitabalans (FI, SE, PL, CZ, SK, SI, DE, DK, EE, LV, LT, HU)

    Date of last revision of the leaflet:28.03.2019

  • Country of registration
  • Active substance
  • Prescription required
    Yes
  • Manufacturer
  • Importer
    Vitabalans Oy

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