Triplixam

Package leaflet: Information for the patient

Warning! Keep this leaflet. The information on the immediate packaging is in a foreign language.
Triplixam, 10 mg + 2.5 mg + 10 mg, coated tablets
Perindoprilum argininum + Indapamidum + Amlodipinum
Please read this leaflet carefully before using the medicine, as it contains
important information for the patient.

• Keep this leaflet, as you may need to read it again.
• If you have any questions, ask your doctor or pharmacist.
• This medicine has been prescribed for a specific individual. Do not pass it on to others. It may harm other people, even if their symptoms are the same.
• If you experience any adverse reactions, including any not listed in this leaflet, inform your doctor, pharmacist, or nurse. See section 4.

Table of contents of the leaflet:

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

1. What Triplixam is and what it is used for

Triplixam is a combination medicine containing three active substances: perindopril,
indapamide, and amlodipine. It is an antihypertensive medicine used to treat high
blood pressure (hypertension).
Patients already taking perindopril and indapamide in one medicine and amlodipine in another may
instead take one Triplixam tablet containing these three active substances at the same doses.
Each of the active substances helps lower blood pressure, and together they enable control of
the patient's blood pressure:

• Perindopril belongs to a group of medicines called angiotensin-converting enzyme (ACE) inhibitors. It works by widening blood vessels, making it easier for the heart to pump blood through them.
• Indapamide is a diuretic (belonging to a group of medicines called sulfonamide derivatives with an indole ring). Diuretics increase the amount of urine produced by the kidneys. However, indapamide differs from other diuretics in that it causes only a slight increase in urine production.
• Amlodipine is a calcium antagonist (belonging to a group of medicines called dihydropyridines). It relaxes blood vessels, allowing blood to flow more easily through them.

2. Important information before taking Triplixam

When not to take Triplixam:

• if the patient is allergic to perindopril or other ACE inhibitors, indapamide or other sulfonamides, amlodipine or other dihydropyridines, or to any of the other ingredients of this medicine (listed in section 6);
• if the patient has previously experienced symptoms during treatment with an ACE inhibitor such as wheezing, facial or tongue swelling, intense itching, or severe rash,

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or if such symptoms occurred in the patient or a family member under any other circumstances
(a condition known as angioedema);

• if the patient has severe liver disease or a condition called hepatic encephalopathy (a brain dysfunction caused by liver disease);
• if untreated, uncontrolled heart failure is suspected in the patient (marked fluid retention, breathing difficulties);
• if the patient has aortic valve stenosis (narrowing of the aorta) or cardiogenic shock (a condition in which the heart cannot deliver sufficient blood to the body);
• if the patient has heart failure following a heart attack;
• if the patient has very low blood pressure (hypotension);
• if the patient has low potassium levels in the blood;
• if the patient has severe kidney disease causing reduced blood flow to the kidneys (renal artery stenosis);
• if the patient is undergoing dialysis or another form of blood filtration. Depending on the equipment used, Triplixam may not be suitable for the patient;
• if the patient has moderate kidney disease;
• after the 3rd month of pregnancy (it is also advisable to avoid using Triplixam early in pregnancy –
• see section on pregnancy);
• if the patient has diabetes or kidney dysfunction and is being treated with a blood pressure-lowering medicine containing aliskiren;
• if the patient has taken or is currently taking a combination medicine containing sacubitril and valsartan, used to treat heart failure, because this increases the risk of angioedema (rapid swelling of tissues under the skin in the throat area) (see "Warnings and precautions" and "Triplixam with other medicines").

Warnings and precautions
If any of the following conditions apply to the patient, consult a doctor or
pharmacist before taking Triplixam:

• if the patient has hypertrophic cardiomyopathy (a heart muscle disease) or renal artery stenosis (narrowing of the blood vessel supplying blood to the kidney);
• if the patient has heart failure or any other heart disease;
• if the patient has a significant increase in blood pressure (hypertensive crisis);
• if the patient has liver disease;
• if the patient has collagenosis (connective tissue disease), such as systemic lupus erythematosus or scleroderma;
• if the patient has atherosclerosis (hardening of the arteries);
• if the patient is undergoing parathyroid function tests;
• if the patient has gout;
• if the patient has diabetes;
• if the patient is on a low-salt diet or uses potassium-containing salt substitutes (maintaining appropriate potassium levels in the blood is important);
• if the patient is taking lithium or potassium-sparing diuretics (spironolactone, triamterene), as these should not be used with Triplixam (see "Triplixam with other medicines");
• if the patient is elderly and the dose needs to be increased;
• if the patient has previously experienced light sensitivity reactions;
• in black patients, angioedema (swelling of the face, lips, mouth, tongue, or throat, which may cause difficulty swallowing or breathing) may occur more frequently, and the medicine may be less effective in lowering blood pressure;
• if the patient is undergoing dialysis using high-flux membranes;
• if the patient has kidney disease or is on dialysis;
• if the patient experiences worsening vision or eye pain. These may be symptoms of fluid accumulation in the choroid layer of the eye (choroidal effusion) or increased intraocular pressure, which may occur within hours or weeks of taking Triplixam. Untreated symptoms may lead to permanent vision loss. If the patient previously had an allergy to penicillin or sulfonamides, the risk of these disorders is higher.

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• if the patient has muscle disorders, including pain, tenderness, weakness, or cramps;
• if the patient has abnormally high levels of a hormone called aldosterone in the blood (primary hyperaldosteronism);
• if there is excessive acid in the blood, which may cause rapid breathing;
• if the patient has cerebral circulatory insufficiency (low blood pressure in the brain);
• if the patient develops swelling of the face, lips, mouth, tongue, or throat, possibly causing difficulty swallowing or breathing (angioedema), which may occur at any time during treatment, treatment must be stopped immediately and medical advice sought.
• if the patient is taking any of the following medicines, as they increase the risk of angioedema:
• racecadotril (used to treat diarrhoea);
• sirolimus, everolimus, temsirolimus, and other medicines belonging to the group of so-called mTOR inhibitors (used to prevent organ transplant rejection and in cancer treatment);
• sacubitril (available in a combination medicine containing sacubitril and valsartan), used to treat chronic heart failure;
• linagliptin, saxagliptin, sitagliptin, vildagliptin, and other medicines belonging to the group of drugs called gliptins (used to treat diabetes);
• if the patient is taking any of the following medicines used to treat high blood pressure:
• an angiotensin II receptor antagonist (AIIRA), also known as a sartan – for example, valsartan, telmisartan, irbesartan, especially if the patient has kidney dysfunction related to diabetes,
• aliskiren. The doctor may recommend regular monitoring of kidney function, blood pressure, and blood electrolyte levels (e.g. potassium). See also the section "When not to take Triplixam".

The doctor may recommend blood tests to assess whether there is a decrease in sodium or potassium levels or an increase in calcium levels.
Inform your doctor if you are pregnant, planning pregnancy, or suspect pregnancy. Use of
Triplixam is not recommended during early pregnancy and must not be taken after the 3rd month of pregnancy, as it may seriously harm the unborn child (see section "Pregnancy and breastfeeding").
When taking Triplixam, inform your doctor or healthcare provider if:

• the patient is to undergo anaesthesia and/or surgery;
• the patient has recently experienced diarrhoea or vomiting, or is dehydrated;
• LDL apheresis (mechanical removal of cholesterol from the blood) is to be performed;
• desensitisation treatment is planned to reduce allergic reactions following bee or wasp stings;
• an imaging test requiring iodine-containing contrast agents (substances allowing visualisation of organs such as the kidney or stomach in X-ray examinations) is to be performed.

Athletes should be aware that Triplixam contains an active substance (indapamide) that
may lead to a positive result in anti-doping tests.
Children and adolescents
Triplixam must not be given to children and adolescents.
Triplixam with other medicines
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Inform your doctor or pharmacist about all medicines currently or recently taken,
as well as any medicines the patient plans to use.
Patients with diabetes or kidney disease must not take aliskiren (used to treat
high blood pressure).
Avoid taking Triplixam with:

• lithium (used to treat certain mental disorders such as mania, bipolar disorder, and recurrent depression);
• potassium-sparing medicines (triamterene, amiloride), potassium supplements, potassium-containing salt substitutes, or other medicines that may increase potassium levels in the body (such as heparin, a blood thinner used to prevent blood clots; trimethoprim and co-trimoxazole, also known as a combination medicine containing trimethoprim and sulfamethoxazole, used to treat bacterial infections);
• dantrolene (intravenous), also used to treat malignant hyperthermia occurring during anaesthesia (symptoms include very high fever and muscle rigidity);
• estramustine (used to treat cancer);
• medicines used to treat diarrhoea (racecadotril) or medicines used to prevent organ transplant rejection (sirolimus, everolimus, temsirolimus, and other medicines belonging to the group of so-called mTOR inhibitors). See section "Warnings and precautions".
• a combination medicine containing sacubitril and valsartan (used to treat chronic heart failure). See sections "When not to take Triplixam" and "Warnings and precautions".
• other medicines used to treat high blood pressure: angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor antagonists.

Other medicines may affect treatment with Triplixam. The doctor may recommend
a dose adjustment and/or additional precautions. Inform your doctor if the patient
is taking any of the following medicines, as this may require special precautions:

• other medicines used to treat high blood pressure, including angiotensin II receptor antagonists (AIIRA), aliskiren (see also sections "When not to take Triplixam" and "Warnings and precautions") or diuretics (medicines that increase urine production by the kidneys);
• potassium-sparing medicines used to treat heart failure: eplerenone and spironolactone at doses from 12.5 mg to 50 mg per day;
• anaesthetics;
• iodine-containing contrast agents;
• bepridil (used to treat angina pectoris);
• methadone (used to treat addiction);
• medicines used to treat heart rhythm disorders (e.g. dofetilide, ibutilide, bretylium, cisapride, difemanyl, procainamide, quinidine, hydroquinidine, disopyramide, amiodarone, sotalol);
• verapamil, diltiazem (used in heart diseases);
• digoxin or other cardiac glycosides (used in heart diseases);
• antibiotics used to treat bacterial infections (e.g. rifampicin, intravenous erythromycin, clarithromycin, sparfloxacin, moxifloxacin);
• antifungal medicines (e.g. itraconazole, ketoconazole, intravenous amphotericin B);
• allopurinol (used to treat gout);
• antihistamines used to treat allergic reactions such as hay fever (e.g. mizolastine, terfenadine, astemizole);
• corticosteroids used to treat various diseases, including severe asthma and rheumatoid arthritis, and non-steroidal anti-inflammatory drugs (e.g. ibuprofen) or high doses of salicylates (e.g. acetylsalicylic acid, a substance found in many medicines used for pain relief, fever reduction, and prevention of blood clots);

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• immunosuppressive medicines (given to control immune system responses) used to treat autoimmune diseases or after organ transplantation (e.g. cyclosporine, tacrolimus);
• tetracosactide (used to treat Crohn's disease);
• gold salts, especially when administered intravenously (used to treat symptoms of rheumatoid arthritis);
• halofantrine (used to treat certain types of malaria);
• baclofen used to treat muscle stiffness occurring in diseases such as multiple sclerosis;
• medicines used to treat diabetes, such as insulin or metformin;
• calcium, including calcium supplements;
• stimulant laxatives (e.g. senna);
• medicines used to treat cancer;
• vinpocetine (used to treat symptomatic cognitive disorders in elderly patients, including memory loss);
• medicines used to treat mental disorders such as depression, anxiety, schizophrenia (e.g. tricyclic antidepressants, antipsychotics, imipramine-type antidepressants, neuroleptics (such as amisulpride, sulpiride, sultopride, tiapride, haloperidol, droperidol));
• pentamidine (used to treat pneumonia);
• ritonavir, indinavir, nelfinavir (so-called protease inhibitors used to treat HIV infections);
• Hypericum perforatum (St. John's wort);
• trimethoprim (used to treat infections);
• medicines used to treat low blood pressure, shock, or asthma (e.g. ephedrine, noradrenaline, or adrenaline);
• nitroglycerin and other nitrates or other vasodilating medicines, as they may further reduce blood pressure.

Triplixam with food and drink
While taking Triplixam, do not consume grapefruit or grapefruit juice,
as this may increase the concentration of the active substance – amlodipine – which may cause
unexpectedly intensified blood pressure-lowering effects of Triplixam.
Pregnancy and breastfeeding
If the patient is pregnant or breastfeeding, suspects she may be pregnant, or plans to have
a child, she should consult a doctor or pharmacist before using this medicine.
Pregnancy
Inform your doctor if you are pregnant, suspect pregnancy, or plan pregnancy. Usually, the doctor will recommend
discontinuing Triplixam before planned pregnancy or immediately after pregnancy is confirmed, and will recommend an alternative medicine instead of Triplixam. Use of Triplixam is not recommended during early pregnancy and must not be taken after the 3rd month of pregnancy, as it may seriously harm the unborn child.
Breastfeeding
Inform your doctor if you are breastfeeding or plan to breastfeed. Use of Triplixam is not recommended during breastfeeding, especially when nursing a newborn or premature infant. The doctor may recommend an alternative medicine.
Driving and operating machinery
Triplixam may affect the ability to drive or operate machinery. If taking the medicine causes nausea, dizziness, fatigue, or headache, do not drive or operate machinery and contact your doctor immediately.
Triplixam contains sodium
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Triplixam contains less than 1 mmol of sodium (23 mg) per tablet, meaning the medicine is considered "sodium-free".

3. How to use Triplixam

This medicine should always be taken exactly as directed by a doctor or pharmacist. If in doubt,
consult a doctor or pharmacist.
Triplixam is available in the following doses:
5 mg + 1,25 mg + 5 mg;
5 mg + 1,25 mg + 10 mg;
10 mg + 2,5 mg + 5 mg;
10 mg + 2,5 mg + 10 mg.
The tablet should be swallowed with a glass of water, preferably in the morning, before a meal. The doctor will determine
the appropriate dose for the patient. Usually, the recommended dose is one tablet once daily.

Taking more Triplixam than prescribed
Taking too many tablets may cause blood pressure to drop, even to dangerous levels, which may sometimes be accompanied by nausea, vomiting, cramps, dizziness, drowsiness, disorientation, oliguria (passing less urine than usual), anuria
(absence of urine production or excretion). The patient may feel a "void" in the head, experience faintness or weakness. If the drop in blood pressure is significant, shock may occur, characterized by cold and clammy skin, and the patient may lose consciousness.
Within 24 to 48 hours after taking the medicine, shortness of breath may develop due to excess fluid accumulating in the lungs (pulmonary edema).
If too many Triplixam tablets have been taken, seek immediate medical attention by contacting a doctor or going to the emergency department of the nearest hospital.

Missing a dose of Triplixam
It is important to take the medicine every day, as regular use ensures more effective treatment. However, if a dose of Triplixam is missed, take the next dose at the usual time. Do not take a double dose to make up for the missed dose.

Stopping Triplixam treatment
Treatment for high blood pressure is usually long-term; therefore, consult a doctor before stopping this medicine.
If you have any further questions about the use of this medicine, consult your doctor or pharmacist.

4. Possible adverse reactions

Like all medicines, this medicine can cause adverse reactions, although not everyone will experience them.
If the patient experiences any of the following serious adverse symptoms, the medicine must be discontinued and medical advice must be sought immediately:

• sudden onset of wheezing, chest pain, shortness of breath or difficulty breathing (uncommon – may affect less than 1 in 100 patients);
• swelling of the eyelids, face or lips (uncommon – may affect less than 1 in 100 patients);
• swelling of the mucous membranes of the mouth, tongue or throat, causing significant breathing difficulties (uncommon – may affect less than 1 in 100 patients);
• severe skin reactions, including severe rash, urticaria, redness of the entire skin surface, intense itching, blistering, peeling and swelling of the skin, mucosal inflammation (Stevens-Johnson syndrome, toxic epidermal necrolysis) or other allergic reactions (very rare – may affect less than 1 in 10,000 patients);
• severe dizziness or fainting (common – may affect less than 1 in 10 patients);
• heart attack (very rare – may affect less than 1 in 10,000 patients), life-threatening heart rhythm disturbances (frequency unknown);
• pancreatitis, which may cause severe upper abdominal pain radiating to the back and general malaise (very rare – may affect less than 1 in 10,000 patients);
• muscle weakness, cramps, tenderness or pain, particularly if the patient also feels unwell or has a high temperature, which may be due to abnormal muscle breakdown (frequency unknown).

Adverse reactions grouped by decreasing frequency of occurrence:

• very common (affects at least 1 in 10 patients): oedema (fluid retention).

• common (affects less than 1 in 10 patients): low blood potassium levels, headache, central dizziness, palpitations (awareness of heartbeat), sudden flushing of the face and neck, labyrinthine dizziness, tingling/numbness, visual disturbance, double vision, tinnitus (perception of ringing or other sounds), sensation of "emptiness" in the head due to low blood pressure, cough, shortness of breath, gastrointestinal disturbances (nausea, vomiting, abdominal pain, taste disturbances, indigestion or digestive disorders, diarrhoea, constipation, changes in bowel rhythm), allergic reactions (such as rashes, itching), muscle cramps, fatigue, weakness, somnolence, swelling of the ankle area.

• uncommon (affects less than 1 in 100 patients): mood swings, anxiety, depression, sleep disturbances, tremor, urticaria, fainting, pain insensitivity, irregular and/or rapid heartbeat, nasal mucosal inflammation (nasal swelling or discharge), hair loss, purpura (small red spots on the skin), skin discoloration, itching, sweating, chest pain, muscle or joint pain, back pain, pain, malaise, kidney disorders, urinary disorders, nocturia (need to urinate at night), increased frequency of urination, impotence (inability to achieve or maintain an erection), fever or elevated body temperature, discomfort or enlargement of the breasts in men, weight gain or weight loss, increased count of a certain type of white blood cells, high blood potassium levels, hypoglycaemia (very low blood sugar levels), low blood sodium levels, which may lead to dehydration and low blood pressure, vasculitis (inflammation of blood vessels), photosensitivity reaction (skin changes) after exposure to sunlight or artificial UVA radiation, clusters of blisters on the skin, swelling of hands or feet, increased blood creatinine and urea levels, falls, dryness of the oral mucosa.

• rare (affects less than 1 in 1,000 patients): disorientation, abnormal laboratory test results: low blood chloride levels, low blood magnesium levels, increased liver enzyme activity, elevated serum bilirubin; exacerbation of psoriasis, reduced or absent urine output, acute kidney failure. Dark-coloured urine, nausea or vomiting, muscle cramps, disorientation and seizures may be symptoms of a condition called SIADH (syndrome of inappropriate antidiuretic hormone secretion).

• very rare (affects less than 1 in 10,000 patients): decreased number of white blood cells, decreased platelet count (leading to easy bruising and nosebleeds), anaemia (reduced number of red blood cells), angina pectoris (chest pain, jaw and back pain triggered by physical exertion and caused by impaired blood supply to the heart), eosinophilic pneumonia (a rare type of lung inflammation), gum swelling, severe skin reactions including severe rash, redness of the entire skin surface, intense itching, blistering, peeling and swelling of the skin, erythema multiforme (rash, often starting with red, itchy spots on the face, arms or legs), bleeding, tender or enlarged gums, liver function disorders, hepatitis, severe kidney dysfunction, yellowing of the skin (jaundice), abdominal distension (gastritis), nerve disorders causing weakness, tingling or numbness, increased muscle tone, hyperglycaemia (very high blood sugar levels), high blood calcium levels, stroke, possibly secondary to a significant drop in blood pressure.

• frequency not known (cannot be estimated from available data): hepatic encephalopathy (brain disorder caused by liver disease), abnormal ECG findings; in patients with systemic lupus erythematosus (a type of collagenosis), symptoms may worsen. Myopia, blurred vision, worsening of vision or eye pain due to high pressure (possible symptoms of fluid accumulation in the choroidal layer of the eye (choroidal effusion) or acute angle-closure glaucoma). Tremor, rigidity, mask-like facial expression, bradykinesia and shuffling gait. Cyanosis, numbness and pain in fingers or toes (Raynaud's phenomenon).

Changes in laboratory test results (blood tests) may occur. Your doctor may recommend blood tests to monitor your health.
If any of these symptoms occur, contact your doctor as soon as possible.
Reporting of adverse reactions
If any adverse symptoms occur, including any not listed in this leaflet, inform your doctor, pharmacist or nurse. Adverse reactions can be reported directly to the Department of Monitoring Adverse Drug Reactions of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products
Al. Jerozolimskie 181C
02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
Reporting adverse reactions helps provide more information on the safety of this medicine.

5. How to store Triplixam

Keep this medicine out of sight and reach of children.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the specified month.
No special storage conditions apply.
Shelf-life after first opening of the container with 30 coated tablets: 30 days.
Medicines must not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer in use. This will help protect the environment.

6. Contents of the pack and other information

What Triplixam contains

• The active substances in the medicine are: perindopril with arginine, indapamide and amlodipine.

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One coated tablet of Triplixam contains 6.790 mg of perindopril (equivalent to 10 mg of perindopril arginine), 2.5 mg of indapamide, and 13.870 mg of amlodipine besylate (equivalent to 10 mg of amlodipine).

• Other components of the tablet are:
• tablet core: calcium carbonate with starch [composition: calcium carbonate (90%), pregelatinized starch, corn (10%)], microcrystalline cellulose, sodium croscarmellose, magnesium stearate, colloidal anhydrous silica, pregelatinized starch, corn.
• tablet coating: glycerol, hypromellose 6 mPas, macrogol 6000, magnesium stearate, titanium dioxide (E 171).

What Triplixam looks like and contents of the pack
Triplixam 10 mg + 2.5 mg + 10 mg: white, elongated, film-coated tablet measuring 12.2 mm in length and

6.46 mm in width, with an embossed mark on one side and an embossed mark on the other side.
Tablets are available in cardboard boxes containing 30, 60 (2 tablet containers with 30 tablets each) or 90 (3 tablet containers with 30 tablets each) tablets.
The container cap contains a moisture-absorbing agent.
For more detailed information, please contact the marketing authorization holder or parallel importer:
Marketing Authorization Holder in Lithuania, country of export:
Les Laboratoires Servier, 50, rue Carnot, 92284 Suresnes cedex, France
Manufacturer:
Servier (Ireland) Industries Ltd, Gorey Road, Arklow - Co. Wicklow, Ireland
Les Laboratoires Servier Industrie, 905 route de Saran, 45520 Gidy, France
Anpharm Przedsiebiorstwo Farmaceutyczne S.A., ul. Annopol 6b, 03-236 Warszawa, Poland
EGIS Pharmaceuticals Private Limited Company, H–9900 Körmend, Mátyás király u.65, Hungary
Parallel importer:
Delfarma Sp. z o.o., ul. Św. Teresy od Dzieciątka Jezus 111, 91-222 Łódź
Repackaged in:
Delfarma Sp. z o.o., ul. Św. Teresy od Dzieciątka Jezus 111, 91-222 Łódź
Marketing Authorization Number in Lithuania, country of export: LT/1/14/3522/021
LT/1/14/3522/023
LT/1/14/3522/024
LT/1/14/3522/042
Parallel Import Authorization Number: 405/25
This medicinal product is authorized for marketing in the European Economic Area member states under the following names:
Belgium TRIPLIXAM, comprimé pelliculé
Bulgaria TRIPLIXAM, филмирани таблетки
Croatia TRIPLIXAM, filmom obložene tablete
Cyprus TRIPLIXAM, επικαλυμμένα με λεπτό υμένιο δισκία
Czech Republic TRIPLIXAM
Estonia TRIPLIXAM
Finland TRIPLIXAM, kalvopäällysteinen tabletti
France TRIPLIXAM, comprimé pelliculé
Greece TRIPLIXAM, επικαλυμμένα με λεπτό υμένιο δισκία
Ireland COVERDINE film-coated tablets
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Italy TRIPLIAM, compresse rivestite con film
Latvia TRIPLIXAM, apvalkotās tabletes
Lithuania TRIPLIXAM, plėvele dengtos tabletės
Luxembourg TRIPLIXAM, comprimé pelliculé
Malta TRIPLIXAM film-coated tablets
Netherlands TRIPLIXAM, filmomhulde tabletten
Poland TRIPLIXAM
Portugal TRIPLIXAM
Romania TRIPLIXAM comprimate filmate
Slovakia TRIPLIXAM, filmom obalené tablety
Slovenia TRIPLIXAM filmsko obložene tablete
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