Package Leaflet: Information for the PatientCoAprovel 150mg/12.5mg film-coated tablets
Irbesartan/Hydrochlorothiazide
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
CoAprovel is a combination of two active substances, irbesartan and hydrochlorothiazide.
Irbesartan belongs to a group of medicines known as angiotensin-II receptor antagonists.
Angiotensin-II is a substance produced by the body which binds to receptors in blood vessels causing them to constrict. This constriction results in an increase in blood pressure. Irbesartan works by blocking the binding of angiotensin-II to these receptors, relaxing blood vessels and thus lowering blood pressure.
Hydrochlorothiazide belongs to a group of medicines called thiazide diuretics, which increase the amount of urine removed from the body and thus lower blood pressure.
The two active ingredients in CoAprovel work together to lower blood pressure more than either medicine alone.
CoAprovel is used to treat high blood pressurewhen treatment with irbesartan or hydrochlorothiazide alone is not sufficient to control blood pressure.
Do not take CoAprovel
Warnings and precautions
Consult your doctor before taking CoAprovel and in the following cases:
Your doctor may check your kidney function, blood pressure, and blood electrolyte levels (e.g., potassium) at regular intervals.
Consult your doctor if you experience abdominal pain, nausea, vomiting, or diarrhea after taking CoAprovel. Your doctor will decide whether to continue treatment. Do not stop taking CoAprovel on your own.
See also the information under the heading “Do not take CoAprovel”.
If you are pregnant, think you may be pregnant, or are planning to have a baby, inform your doctor. CoAprovel is not recommended during the first three months of pregnancy and must not be taken after the third month of pregnancy as it may cause serious harm to your baby (see section “Pregnancy”).
You must also inform your doctor:
Hydrochlorothiazide contained in this medicine may cause positive results in doping control.
Children and adolescents
CoAprovel should not be given to children and adolescents (under 18 years of age).
Using CoAprovel with other medicines
Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines.
Diuretics, such as hydrochlorothiazide contained in CoAprovel, may have an effect on other medicines. Do not take preparations containing lithium with CoAprovel without your doctor's supervision.
Your doctor may need to change your dose and/or take other precautions:
If you are taking an angiotensin-converting enzyme inhibitor (ACE inhibitor) or aliskiren (see also the information under the headings “Do not take CoAprovel” and “Warnings and precautions”).
You may need to have blood tests if you take:
It is also important to inform your doctor if you are taking other medicines to lower your blood pressure, steroids, medicines to treat cancer, painkillers, medicines for arthritis, or cholestyramine or colestipol resins to lower cholesterol in the blood.
Taking CoAprovel with food, drinks, and alcohol
CoAprovel can be taken with or without food.
Due to the hydrochlorothiazide contained in CoAprovel, if you drink alcohol while being treated with this medicine, you may have an increased feeling of dizziness when standing up, especially when getting up from a sitting or lying position.
Pregnancy, breastfeeding, and fertility
Pregnancy
You should inform your doctor if you are pregnant, think you might be pregnant, or are planning to have a baby. Your doctor will normally advise you to stop taking CoAprovel before you become pregnant or as soon as you know you are pregnant and will advise you to take another medicine to treat your high blood pressure. CoAprovel is not recommended during the first three months of pregnancy and must not be taken after the third month of pregnancy as it may cause serious harm to your baby.
Breastfeeding
Inform your doctor if you are about to start or are already breastfeeding, as CoAprovel is not recommended for use during breastfeeding. Your doctor may decide to prescribe a different treatment that is more suitable if you want to breastfeed, especially for newborns or premature babies.
Driving and using machines
CoAprovel is unlikely to affect your ability to drive or use machines. However, during treatment for high blood pressure, dizziness or fatigue may occasionally occur. If you experience these symptoms, talk to your doctor before driving or using machines.
CoAprovel contains lactose. If your doctor has told you that you have an intolerance to some sugars, contact them before taking this medicine.
CoAprovel contains sodium. This medicine contains less than 1 mmol of sodium (23 mg) per tablet, which is essentially “sodium-free”.
Always take this medicine exactly as your doctor has told you. If you are not sure, check with your doctor or pharmacist.
Dose
The recommended dose of CoAprovel is one or two tablets a day. In general, your doctor will prescribe CoAprovel when previous treatments you have taken have not sufficiently controlled your blood pressure. Your doctor will tell you how to switch from your previous treatments to CoAprovel.
Method of administration
CoAprovel is taken by mouth. The tablets should be swallowed with a sufficient amount of liquid (e.g., a glass of water). You can take CoAprovel with or without food. Try to take your daily dose at the same time each day. It is important that you continue to take CoAprovel until your doctor tells you to stop.
The maximum blood pressure-lowering effect should be achieved after 6-8 weeks of treatment.
If you take more CoAprovel than you should
If you accidentally take too many tablets, contact your doctor immediately.
Children should not take CoAprovel
CoAprovel should not be given to children under 18 years of age. If a child swallows some tablets, contact your doctor immediately.
If you forget to take CoAprovel
If you accidentally miss a dose, simply take your normal dose when it is due. Do not take a double dose to make up for a forgotten dose.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, CoAprovel can cause side effects, although not everybody gets them.
Some of these effects can be serious and may require medical attention.
Rarely, cases of allergic skin reactions (skin rash, urticaria) have been reported in patients treated with irbesartan, as well as localized swelling of the face, lips, and/or tongue. If you have any of these symptoms or experience difficulty breathing, stop taking CoAprovel and contact your doctor immediately.
The frequency of side effects is defined using the following convention:
Common: may affect up to 1 in 10 people
Uncommon: may affect up to 1 in 100 people
The side effects reported in clinical trials for patients treated with CoAprovel were:
Common side effects(may affect up to 1 in 10 people):
If any of these side effects get serious, talk to your doctor
Uncommon side effects(may affect up to 1 in 100 people):
If any of these side effects get serious, talk to your doctor
Side effects reported since CoAprovel has been marketed
Since CoAprovel has been marketed, the following side effects have been reported. The frequency of these side effects is not known: headache, ringing in the ears, cough, altered taste, indigestion, muscle and joint pain, liver function disorders, kidney failure, high levels of potassium in the blood, and allergic reactions such as skin rash, urticaria, swelling of the face, lips, mouth, tongue, or throat. Rare cases of jaundice (yellowing of the skin and/or whites of the eyes) have also been reported.
As with all combinations of two active substances, it cannot be excluded that side effects associated with each of the components may occur.
Side effects associated with irbesartan alone
In addition to the side effects described above, the following have also been reported: chest pain, severe allergic reactions (anaphylactic shock), decreased red blood cell count (anemia - symptoms may include tiredness, headaches, difficulty breathing when exercising, dizziness, and paleness), and decreased platelet count, as well as low blood sugar levels. Rare (may affect up to 1 in 1,000 people): intestinal angioedema: swelling in the intestine that presents with symptoms such as abdominal pain, nausea, vomiting, and diarrhea.
Side effects associated with hydrochlorothiazide alone
Loss of appetite; stomach upset; stomach cramps; constipation; jaundice (yellowing of the skin and/or whites of the eyes); pancreatitis characterized by severe upper stomach pain, often with nausea and vomiting; sleep disorders; depression; blurred vision; low white blood cell count, which can lead to frequent infections, fever; decreased platelet count, decreased red blood cell count (anemia) characterized by tiredness, headaches, difficulty breathing when exercising, dizziness, and paleness; kidney disease; lung disorders including pneumonia or fluid accumulation in the lungs; increased sensitivity of the skin to the sun; blood vessel inflammation; a skin disease characterized by peeling of the skin all over the body; cutaneous lupus erythematosus, which is identified by a rash that can appear on the face, neck, and scalp; allergic reactions; weakness and muscle spasms; irregular heartbeat; low blood pressure after changing body position; swelling of the salivary glands; high blood sugar levels; sugar in the urine; increased levels of certain fats in the blood; high levels of uric acid in the blood, which can cause gout.
Very rare:Acute respiratory distress (signs include severe difficulty breathing, fever, weakness, and confusion).
Frequency “not known”(cannot be estimated from the available data): Skin and lip cancer (non-melanoma skin cancer), decreased vision or eye pain due to high pressure (possible signs of fluid accumulation in the vascular layer of the eye (choroidal effusion) or acute angle-closure glaucoma).
It is known that side effects associated with hydrochlorothiazide can increase with higher doses of hydrochlorothiazide.
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system listed in Appendix V. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton and on the blister after EXP. The expiry date refers to the last day of the month shown.
Do not store above 30 °C.
Store in the original packaging to protect from moisture.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Composition of CoAprovel
Appearance and package contents of the product
The film-coated tablets of CoAprovel 150 mg/12.5 mg are peach, biconvex, oval-shaped, with a heart-shaped indentation on one side and the number 2875 engraved on the other.
CoAprovel 150 mg/12.5 mg film-coated tablets are available in blister packs of 14, 28, 30, 56, 84, 90 or 98 film-coated tablets. They are also available in unit dose blister packs of 56 x 1 film-coated tablet for hospital use.
Not all pack sizes may be marketed.
Marketing authorisation holder
Sanofi Winthrop Industrie
82 avenue Raspail
94250 Gentilly
France
Manufacturer
SANOFI WINTHROP INDUSTRIE1, rue de la ViergeAmbarès & LagraveF‑33565 Carbon Blanc Cedex - France
SANOFI WINTHROP INDUSTRIE30-36 Avenue Gustave Eiffel37100 Tours - France
SANOFI-AVENTIS, S.A.
Ctra. C-35 (La Batlloria-Hostalric), km. 63.09
17404 Riells i Viabrea (Girona)
Spain
For further information about this medicine, please contact the local representative of the marketing authorisation holder:
België/Belgique/Belgien Sanofi Belgium Tel: +32 (0)2 710 54 00 | Luxembourg/Luxemburg Sanofi Belgium Tel: +32 (0)2 710 54 00 (Belgique/Belgien) |
Magyarország sanofi-aventis zrt., Magyarország Tel.: +36 1 505 0050 | |
Ceská republika Sanofi, s.r.o. Tel: +420 233 086 111 | Malta Sanofi S.r.l. Tel: +39 02 39394275 |
Danmark Sanofi A/S Tlf: +45 45 16 70 00 | Nederland Sanofi B.V. Tel: +31 20 245 4000 |
Deutschland Sanofi-Aventis Deutschland GmbH Tel: 0800 52 52 010 Tel. from abroad: +49 69 305 21 131 | Norge sanofi-aventis Norge AS Tlf: +47 67 10 71 00 |
Eesti Swixx Biopharma OÜ Tel: +372 640 10 30 | Österreich sanofi-aventis GmbH Tel: +43 1 80 185 – 0 |
Ελλάδα Sanofi-Aventis Μονοπρ?σωπη AEBE Τηλ: +30 210 900 16 00 | Polska Sanofi Sp. z o.o. Tel.: +48 22 280 00 00 |
España sanofi-aventis, S.A. Tel: +34 93 485 94 00 | Portugal Sanofi - Produtos Farmacêuticos, Lda Tel: +351 21 35 89 400 |
France Sanofi Winthrop Industrie Tél: 0 800 222 555 Appel depuis l’étranger: +33 1 57 63 23 23 Hrvatska Swixx Biopharma d.o.o. Tel:+385 1 2078 500 | România Sanofi Romania SRL Tel: +40 (0) 21 317 31 36 |
Ireland sanofi-aventis Ireland Ltd. T/A SANOFI Tel: +353 (0) 1 403 56 00 | Slovenija Swixx Biopharma d.o.o. Tel: +386 1 235 51 00 |
Ísland Vistor hf. Sími: +354 535 7000 | Slovenská republika Swixx Biopharma s.r.o. Tel: +421 2 208 33 600 |
Italia Sanofi S.r.l. Tel: 800.536389 | Suomi/Finland Sanofi Oy Puh/Tel: +358 (0) 201 200 300 |
Κύπρος C.A. Papaellinas Ltd. Τηλ: +357 22 741741 | Sverige Sanofi AB Tel: +46 (0)8 634 50 00 |
Latvija Swixx Biopharma SIA Tel: +371 6616 47 50 | United Kingdom (Northern Ireland) sanofi-aventis Ireland Ltd. T/A SANOFI Tel: +44 (0) 800 035 2525 |
Lietuva Swixx Biopharma UAB Tel: +370 5 236 91 40 |
Date of last revision of this leaflet:
Detailed information on this medicine is available on the European Medicines Agency web site: http://www.ema.europa.eu.
The average price of COAPROVEL 150 mg/12.5 mg FILM-COATED TABLETS in October, 2025 is around 9.65 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.