Package Leaflet: Information for the User
Copalia 5mg/80mg film-coated tablets
Copalia 5mg/160mg film-coated tablets
Copalia 10mg/160mg film-coated tablets
amlodipino/valsartán
Read this leaflet carefully before you start taking this medicine because it contains important information for you.
-This medicine has been prescribed for you only, and you must not give it to others even if they have the same symptoms of disease as you, as it may harm them.
-If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this leaflet.See section4.
1.What isCopaliaand what it is used for
2.What you need to know before you start takingCopalia
3.How to takeCopalia
4.Possible side effects
5.Storage ofCopalia
6.Contents of the pack and additional information
Copaliatablets contain two substances called amlodipine and valsartan. Both substances help control high blood pressure.
This means that both substances help prevent blood vessel constriction. As a result, blood vessels relax and blood pressure decreases.
Copaliais used to treat high blood pressure in adults whose blood pressure is not adequately controlled with amlodipine or valsartan alone.
Do not take Copalia
Do not take Copalia and inform your doctorif you are affected by any of the above cases.
Warnings and precautions
Consult your doctor before starting to take Copalia:
Your doctor may monitor your kidney function, blood pressure, and electrolyte levels (such as potassium) at regular intervals.
See also the information under the heading "Do not take Copalia".
Inform your doctor before taking Copalia if you are affected by any of the cases mentioned.
Children and adolescents
Copalia is not recommended for use in children or adolescents (under 18 years old).
Other medications and Copalia
Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication. Your doctor may need to adjust your dose and/or take other precautions. In some cases, you may need to stop taking one of the medications. This applies especially to the medications listed below:
Taking Copalia with food and drinks
People taking Copalia should not consume grapefruit or grapefruit juice. This is because grapefruit and grapefruit juice may increase the levels of the active ingredient amlodipine in the blood, which may cause unpredictable reductions in blood pressure.
Pregnancy and breastfeeding
Pregnancy
Inform your doctor if you are pregnant, if you suspect you may be pregnant, or if you plan to become pregnant.Generally, your doctor will advise you to stop taking Copalia before becoming pregnant or as soon as you become pregnant, and recommend taking another antihypertensive medication instead.It is not recommended to use Copalia at the beginning of pregnancy (first 3 months) and in any case, it should not be administered from the third month of pregnancy as it may cause severe damage to your baby when administered from that point onwards.
Breastfeeding
Inform your doctor if you are planning to start or are currently breastfeeding.Copalia has been shown to pass into breast milk in small amounts.It is not recommended to administer Copalia to women during this period. Your doctor may decide to administer a more suitable treatment if you want to breastfeed, especially for newborns or premature babies.
Consult your doctor or pharmacist before using any medication.
Driving and operating machinery
Copalia may cause dizziness, which may affect your ability to concentrate. Therefore, if you are unsure how this medication will affect you, do not drive, operate machinery, or perform other activities that require concentration.
Follow exactly the administration instructions for this medication as indicated by your doctor. In case of doubt, consult your doctor again. This will help you obtain the best results and reduce the risk of adverse effects.
The usual dose ofCopaliais one tablet per day.
Your doctor may suggest a higher or lower dose depending on your response to treatment.
Do not exceed the prescribed dose.
Copalia and Older Adults (65 years or older)
Your doctor should exercise caution when increasing the dose.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
If You Take More Copalia Than You Should
If you have taken too many tablets ofCopalia, or if someone else has taken your tablets, consult a doctor immediately.Excess fluid can accumulate in the lungs (pulmonary edema) causing breathing difficulty that may develop within 24-48hours after ingestion.
If You Forget to Take Copalia
If you forget to take this medication, take it as soon as you remember. Then take the next dose at the usual time. However, if it is almost time for the next dose, do not take the missed dose. Do not take a double dose to make up for the missed doses.
If You Discontinue Treatment with Copalia
Discontinuing your treatment withCopaliamay cause your condition to worsen. Do not stop taking your medication unless your doctor tells you to.
Like all medications,Copaliamay cause side effects, although not everyone will experience them.
Some side effects can be severe and require immediate medical attention:
A few patients have experienced these severe side effects.Notify your doctor if you notice any of the following:
the following, report them to your doctor right away:
Rare (may affect up to 1 in 1,000 patients):allergic reaction with symptoms such as skin rash, itching, facial swelling, lip or tongue swelling, difficulty breathing, low blood pressure (dizziness, fainting).
Very rare (may affect up to 1 in 10,000 patients):intestinal angioedema: intestinal swelling accompanied by symptoms such as abdominal pain, nausea, vomiting, and diarrhea.
Other possible side effects of Copalia:
Frequent (may affect up to 1 in 10 patients):flu; stuffy nose, sore throat, and discomfort swallowing; headache; swelling in the arms, hands, legs, ankles, or feet; fatigue; asthenia (weakness); facial flushing and/or neck warmth.
Infrequent (may affect up to 1 in 100 patients):dizziness; nausea and abdominal pain; dry mouth; somnolence, paresthesia (tingling) or numbness of the hands or feet; vertigo, rapid heartbeat including palpitations; dizziness upon standing; cough; diarrhea; constipation; skin rash, skin redness; joint inflammation, back pain; joint pain.
Rare (may affect up to 1 in 1,000 patients):anxiety; tinnitus (ringing in the ears); fainting; increased urine production or urgent need to urinate; inability to achieve or maintain an erection; feeling of heaviness; low blood pressure with symptoms such as dizziness, fainting; excessive sweating; skin rash all over the body, itching, muscle spasms.
Notify your doctor if you are severely affected by any of the cases mentioned.
Side effects reported with amlodipine or valsartan alone and not observed with Copalia or observed with a higher frequency than with Copalia:
Amlodipine
Consult your doctor immediately if you experience any of the following severe side effects, which are very rare after taking this medication:
The following side effects have been reported. If any of these cause problems or last more than a week, consult your doctor.
Frequent (may affect up to 1 in 10 patients):dizziness, somnolence; palpitations (feeling the heartbeat); hot flashes, swelling of the ankles (edema); abdominal pain, feeling unwell (nausea).
Infrequent (may affect up to 1 in 100 patients):mood changes, anxiety, depression, somnolence, tremor, taste alterations, fainting, loss of pain sensation; visual disturbances, visual deterioration, tinnitus; decreased blood pressure; nasal congestion or secretion caused by inflammation of the nasal mucosa (rhinitis); indigestion, vomiting (discomfort); hair loss, increased sweating, itching skin, skin discoloration; urinary disorders, increased need to urinate at night, increased frequency of urination; inability to achieve an erection, breast discomfort or enlargement in men, pain, discomfort, muscle pain, muscle cramps; weight gain or loss.
Rare (may affect up to 1 in 1,000 patients):confusion.
Very rare (may affect up to 1 in 10,000 patients):decreased white blood cell count, decreased platelet count that can cause easy bruising or unusual bruising (damage to red blood cells); hyperglycemia (excess glucose in the blood).
Valsartan
Unknown frequency (frequency cannot be estimated from available data):decreased red blood cell count, fever, sore throat or ulcers in the mouth due to infection; spontaneous bleeding or bruising; increased potassium in the blood; abnormal liver function test results; decreased kidney function and severely decreased kidney function; swelling, mainly of the face and throat; muscle pain; skin rash, red spots (purpura); fever; itching; allergic reaction, blistering skin disease (sign of a disease called dermatitis bullosa).
Notify your doctor if you experience any of the cases mentioned.
Notify your doctor or pharmacist if you experience any side effects, even if they are not listed in this prospectus.
Reporting side effects
If you experienceany type of side effect, consult your doctor or pharmacist, even if it is apossibleside effect not listed in this prospectus.You can also report them directlythrough the national notification system included in theAnexo V. By reporting side effects, you can contribute to providing more information about the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the box and the blister pack.
Do not store above30°C.
Store in the original packaging to protect it from moisture.
Do not useCopaliaif you observe that the packaging is damaged or shows signs of tampering.
Copalia 5mg/80mg film-coated tablets
The active ingredients ofCopaliaare amlodipine (as amlodipine besylate) and valsartan. Each tablet contains5mg of amlodipine and 80mg of valsartan.
The other components are microcrystalline cellulose; crospovidone (type A); anhydrous colloidal silica; magnesium stearate; hypromellose(type of substitution 2910 (3 mPa.s)); macrogol 4000; talc, titanium dioxide (E171); yellow iron oxide (E172).
Copalia 5mg/160mg film-coated tablets
The active ingredients ofCopaliaare amlodipine (as amlodipine besylate) and valsartan. Each tablet contains 5mg of amlodipine and 160mg of valsartan.
The other components are microcrystalline cellulose, crospovidone (type A); anhydrous colloidal silica; magnesium stearate; hypromellose(type of substitution 2910 (3 mPa.s)); macrogol 4000; talc, titanium dioxide (E171); yellow iron oxide (E172).
Copalia 10mg/160mg film-coated tablets
The active ingredients ofCopaliaare amlodipine (as amlodipine besylate) and valsartan. Each tablet contains 10mg of amlodipine and 160mg of valsartan.
The other components are microcrystalline cellulose, crospovidone (type A), anhydrous colloidal silica; magnesium stearate; hypromellose(type of substitution 2910 (3 mPa.s)); macrogol 4000; talc, titanium dioxide (E171); yellow iron oxide (E172), red iron oxide (E172).
Appearance of the product and contents of the pack
Copalia5mg/80mg tablets are round and dark yellow in color with«NVR»on one side and«NV»on the other side.Approximate size: diameter 8.20mm.
Copalia5mg/160mg tablets are oval and dark yellow in color with«NVR»on one side and«ECE»on the other side.Approximate size::14.2mm (length) x 5.7mm (width).
Copalia10mg/160mg tablets are oval and light yellow in color with«NVR»on one side and«UIC»on the other side.Approximate size::14.2mm (length) x 5.7mm (width).
Copaliais available in packs containing 7, 14, 28, 30, 56, 90, 98 or 280tablets and in multiple packs containing 4boxes, each containing70tablets, or 20boxes, each containing 14tablets.All packs are available with standard blisters; packs of56, 98 and 280tablets are also available with perforated unit blisters.
Not all pack sizes may be marketed in your country.
Marketing Authorisation Holder
Novartis Europharm Limited
Vista Building
Elm Park, Merrion Road
Dublin 4
Ireland
Responsible for manufacturing
Novartis Farma S.p.A.
Via Provinciale Schito 131
80058 Torre Annunziata (NA)
Italy
Novartis Farmacéutica SA
Gran Via de les Corts Catalanes, 764
08013 Barcelona
Spain
Novartis Pharma GmbH
Roonstraße 25
D-90429 Nuremberg
Germany
Novartis Pharma GmbH
Sophie-Germain-Strasse 10
90443 Nürnberg
Germany
For further information about this medicinal product, please contact the local representative of the marketing authorisation holder:
België/Belgique/Belgien Novartis Pharma N.V. Tél/Tel: +32 2 246 16 11 | Lietuva SIA Novartis Baltics Lietuvos filialas Tel: +370 5 269 16 50 |
Luxembourg/Luxemburg Novartis Pharma N.V. Tél/Tel: +32 2 246 16 11 | |
Ceská republika Novartis s.r.o. Tel: +420 225 775 111 | Magyarország Novartis Hungária Kft. Pharma Tel.: +36 1 457 65 00 |
Danmark Novartis Healthcare A/S Tlf: +45 39 16 84 00 | Malta Novartis Pharma Services Inc. Tel:+356 2122 2872 |
Deutschland Novartis Pharma GmbH Tel: +49 911 273 0 | Nederland Novartis Pharma B.V. Tel: +31 26 37 82 111 |
Eesti SIA Novartis Baltics Eesti filiaal Tel: +372 66 30 810 | Norge Novartis Norge AS Tlf: +47 23 05 20 00 |
Ελλ?δα Novartis (Hellas) A.E.B.E. Τηλ: +30 210 281 17 12 | Österreich Novartis Pharma GmbH Tel: +43 1 86 6570 |
España Vifor Pharma España, S.L. Tel: +34 902 12 11 11 | Polska Novartis Poland Sp. z o.o. Tel.:+48 22 375 4888 |
France Novartis Pharma S.A.S. Tél: +33 1 55 47 66 00 | Portugal Bialport-Produtos Farmacêuticos, S.A. Tel: +351 22 986 61 00 |
Hrvatska Novartis Hrvatska d.o.o. Tel. +385 1 6274 220 | România Novartis Pharma ServicesRomania SRL Tel: +40 21 31299 01 |
Ireland Novartis Ireland Limited Tel: +353 1 260 12 55 | Slovenija Novartis Pharma Services Inc. Tel: +386 1 300 75 50 |
Ísland Vistor hf. Sími: +354 535 7000 | Slovenská republika Novartis Slovakia s.r.o. Tel: +421 2 5542 5439 |
Italia Novartis Farma S.p.A. Tel: +39 02 96 54 1 | Suomi/Finland Novartis Finland Oy Puh/Tel:+358 (0)10 6133 200 |
Κ?προς Novartis Pharma Services Inc. Τηλ: +357 22 690 690 | Sverige Novartis Sverige AB Tel: +46 8 732 32 00 |
Latvija SIA “Novartis Baltics” Tel: +371 67 887 070 |
Last update of this summary:
Other sources of information
The detailed information on this medicinal product is available on the website of the European Medicines Agency:http://www.ema.europa.eu
Маєте питання щодо цього лікування або ваших симптомів? Зв'яжіться з ліцензованим лікарем для отримання допомоги та персонального догляду.