Leaflet: information for the user
ACOVIL 10 mg tablets
Ramipril
Read this leaflet carefully before you start taking this medicine, because it contains important information for you.
Acovil contains a medication called ramipril. This belongs to a group of medications called angiotensin-converting enzyme (ACE) inhibitors.
Acovil works as follows:
Acovil may be used:
Do not take Acovil
The symptoms of an allergic reaction may include skin rash, difficulty swallowing or breathing, swelling of your lips, face, throat, or tongue.
Do not take Acovil if any of the above conditions apply to you. If you are unsure, speak with your doctor before taking Acovil.
- an angiotensin II receptor antagonist (ARA) (also known as “sartanes” - for example, valsartán, telmisartán, irbesartán), particularly if you have kidney problems related to diabetes.
- aliskirén.
Your doctor may need to monitor your kidney function, blood pressure, and electrolyte levels in your blood (such as potassium) at regular intervals. See also the information under the heading “Do not take Acovil”.
Children and adolescents
The use of Acovil in children and adolescents under 18 years of age is not recommended because the safety and efficacy of Acovil in children have not been established.
If any of the above conditions apply to you (or you are unsure), speak with your doctor before taking Acovil.
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication. This is because Acovil may affect how other medications work. Similarly, some medications may affect how Acovil works.
Inform your doctor if you have taken or are taking any of the following medications, which may make Acovil less effective:
Inform your doctor if you are taking any of the following medications. These may increase the risk of side effects if taken with Acovil:
Inform your doctor if you are taking any of the following medications. These may be affected by Acovil:
If any of the above conditions apply to you (or you are unsure), speak with your doctor before taking Acovil.
Taking Acovil with food and alcohol
Pregnancy and breastfeeding
Pregnancy
You should inform your doctor if you are pregnant (or suspect you may be).
You should not take Acovil during the first 12 weeks of pregnancy and should not take it at all from week 13, as its use during pregnancy may cause harm to your baby. If you become pregnant while taking Acovil, inform your doctor immediately. A suitable alternative treatment should be changed before planning a pregnancy.
Breastfeeding
You should not take Acovil if you are breastfeeding.
Consult your doctor or pharmacist before using any medication.
You may feel dizzy while taking Acovil, which is more likely to occur when you start taking Acovil or when you start taking a higher dose of Acovil. If this happens, do not drive or operate tools or machines.
Acovil contains sodium
This medication contains less than 23 mg of sodium (1mmol) per tablet; it is essentially “sodium-free”.
Follow exactly the administration instructions of this medication as indicated by your doctor. Consult your doctor or pharmacist if you have any doubts.
How much medication to take
Hypertension treatment
To reduce the risk of suffering a heart attack or stroke
Treatment to reduce or delay the worsening of kidney problems
Treatment for heart failure
Treatment after having had a heart attack
Older patients
Your doctor will reduce the initial dose and adjust your treatment more slowly.
Taking this medication
If you take more Acovil than you should
Consult your doctor immediately or go to the nearest hospital emergency room. Do not drive to the hospital, ask someone to take you or call an ambulance. Bring the medication packaging with you. This way, your doctor will know what you have taken.
You can also call the Toxicological Information Service, phone 91 562 04 20 indicating the medication and the amount ingested.
If you forgot to take Acovil
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
Stop taking Acovil and seek immediate medical attention if you notice any of the following severe side effects, which may require urgent medical treatment:
Inform your doctor immediately if you experience:
Other side effects include:
Inform your doctor if any of the following worsen or last more than a few days.
Frequent(may affect up to 1 in 10 patients)
Rare(may affect up to 1 in 100 patients)
Very rare(may affect up to 1 in 10,000 patients)
Other side effects reported:
Inform your doctor if any of the following worsen or last more than a few days.
Reporting of side effects
If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through theSpanish System for Pharmacovigilance of Medicines for Human Use:https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep out of sight and reach of children.
Do not use this medication after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated. This medication does notrequire special storage conditions.
Medicines should not be disposed of through drains or in the trash. Dispose of packaging and unused medicines at thepharmacy's SIGREdrop-off point. If in doubt, ask your pharmacist how to dispose of unused packaging and medicines. By doing so, you will help protect the environment.
Composition of Acovil
The active ingredient is ramipril.
10 mg: Each tablet contains 10 mg of ramipril.
The other components are:
Hypromellose
Pre-gelatinized cornstarch
Microcrystalline cellulose
Sodium stearyl fumarate.
Appearance of the product and contents of the package
Oblong-shaped tablets of 7 x 4.5 mm, white to off-white in color, with a notch and marked on the upper face with HMO/HMO. The tablet can be divided into equal doses.
Acovil 10 mg tablets are presented in blisters of 7, 10, 14, 15, 18, 20, 28, 30, 45, 50, 56, 90, 98, 99, 100, 300, 320, 500 tablets in aluminum/PVC blisters.
Not all package sizes may be marketed.
Marketing authorization holder and responsible manufacturer
The marketing authorization holder is:
sanofi-aventis, S.A.
C/ Roselló i Porcel, 21
08016 Barcelona
Spain
The manufacturer is:
Sanofi S.r.l.
Strada Statale 17 km 22
67019 Scoppito (L’Aquila) Italy
Delpharm Dijon
6, Boulevard de L’Europe Quetigny F-21800 France
S.C. ZENTIVA S.A.,
B-dul Theodor Pallady nr. 50, Sector 3, Bucuresti, 032266–Romania
Sanofi Aventis Deutschland GmbH,
Industriepark Höechst Brüningstraβe 50, 65926 Frankfurt am Main, Germany
This medicinal product is authorized in the Member States of the European Economic Area under the following names:
Austria:
Tritace 1.25mgTabletten, Tritace 2.5mgTabletten, Tritace 5mgTabletten, Tritace 10mgTabletten
Bélgica:
Tritace 2.5mgtabletten/comprimés/Tabletten, Tritace 5mgtabletten/comprimés/Tabletten, Tritace 10mgtabletten/comprimés/Tabletten
Bulgaria:
Tritace 5mg????????, Tritace 10mg????????
Chipre:
Triatec 2.5mgδισκ?α, Triatec 5mgδισκ?α
República Checa:
Tritace 1.25mgtablety, Tritace 2.5mgtablety, Tritace 5mgtablety, Tritace 10mgtablety
Dinamarca:
Triatec 5mgtabletter
Estonia:
Cardace 2.5mgtabletid, Cardace 5mgtabletid, Cardace 10mgtabletid
Finlandia:
Cardace 2.5mgtabletit, Cardace 5mgtabletit, Cardace 10mgtabletit
Francia:
Triatec 1.25mgcomprimé, Triatec 2.5mgcomprimé sécable, Triatec 5mgcomprimé sécable, Triatec 10mgcomprimé sécable
Alemania:
Delix 2.5mgTabletten, Delix 5mgTabletten, Delix Protect 10mgTabletten
Delix Protect Startset
Delix 1.25mgTabletten,
Delix 1.25mgKapseln, Delix P 2.5mgKapseln, Delix P 5mgKapseln, Delix P 10mgKapseln
Grecia:
Triatec 2.5mgδισκ?α, Triatec 5mgδισκ?α
Hungría:
Tritace Mite 1.25mgtabletta
Tritace 2.5mgtabletta, Tritace 5mgtabletta, Tritace 10mgtabletta
Irlanda:
Tritace 1.25mgtabs, Tritace 2.5mgtabs, Tritace 5mgtabs, Tritace 10mgtabs,
Italia:
Triatec 2.5mgcompresse, Triatec 5mgcompresse, Triatec 10mgcompresse
Latvia:
Cardace 2.5mgtabletes, Cardace 5mgtabletes, Cardace 10mgtabletes
Lituania:
Cardace 5mgtabletes, Cardace 10mgtabletes
Luxemburgo:
Tritace 2.5mgtabletten/comprimés/Tabletten, Tritace 5mgtabletten/comprimés/Tabletten, Tritace 10mgtabletten/comprimés/Tabletten,
Noruega:
Triatec 2.5mgtabletter, Triatec 5mgtabletter, Triatec 10mgtabletter
Polonia:
Tritace 2.5mgtabletki, Tritace 5mgtabletki, Tritace 10mgtabletki
Portugal:
Triatec 1.25mgcápsulas, Triatec 2.5mgcápsulas, Triatec 5mgcápsulas, Triatec 10mgcápsulas
Rumania:
Tritace 2.5mgcomprimate, Tritace 5mgcomprimate, Tritace 10mgcomprimate
Republic Eslovaca:
Tritace 1.25mgtablety, Tritace 2.5mgtablety, Tritace 5mgtablety, Tritace 10mgtablety
Eslovenia:
Tritace 1.25mgtablete, Tritace 2.5mgtablete, Tritace 5mgtablete, Tritace 10mgtablete
España:
Acovil 2,5 mgcomprimidos, Acovil 5 mgcomprimidos, Acovil 10 mgcomprimidos
Suecia:
Triatec 2.5mgtabletter, Triatec 5mgtabletter, Triatec 10mgtabletter
Reino Unido:
Tritace 1.25mgtablets, Tritace 2.5mgtablets, Tritace 5mgtablets, Tritace 10mgtablets,
Tritace Titration Pack tablets
Last review date of this leaflet: June 2021
For detailed and updated information on this medicinal product, please visit the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/.
The average price of Acovil 10 mg comprimidos in July, 2025 is around 9.68 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.
Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.