Leaflet: information for the user
VIVACE 30 mg/10 mg tablets
delapril hydrochloride + manidipine hydrochloride
Read the entire leaflet carefully before starting to take this medication, as it contains important information for you.
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Contents of the leaflet:
Vivace is
Vivace is a combination of two active substances, delapril hydrochloride and manidipine hydrochloride.
Delapril belongs to a group of medications called angiotensin-converting enzyme inhibitors (ACE inhibitors). Angiotensin II is a substance produced in the body that causes blood vessels to constrict. This leads to an increase in blood pressure. Delapril hydrochloride prevents the production of angiotensin II, which causes a decrease in blood pressure.
Manidipine belongs to a group of medications called calcium channel blockers, which block the flow of calcium into the smooth muscle cells of blood vessels, causing the blood vessels to relax, resulting in a reduction in blood pressure.
The two active substances in Vivace work together to lower blood pressure more effectively than if they were given separately.
Vivace is used for
the treatment of high blood pressure (hypertension) in patients whose blood pressure is not adequately controlled with delapril or manidipine alone.
Do not takeVivace:
Do not give Vivace to children or adolescents under 18 years of age.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Vivace
Sirolimus, everolimus, and other medications belonging to the mTOR inhibitor family (used to prevent organ rejection)
Your doctor may monitor your kidney function, blood pressure, and blood electrolyte levels (e.g., potassium) at regular intervals.
See also the information under the heading "Do not take Vivace".
Children and adolescents
Do not give Vivace to children or adolescents under 18 years of age.
Taking Vivace with other medications
Tell your doctor or pharmacist if you are taking, have recently taken, or may take any other medication, including those obtained without a prescription.
Your doctor may need to adjust your dose and/or take other precautions if you are taking any of the following medications:
Tell your doctor if you are also taking:
Taking Vivace with food and drinks
Vivace should be taken after breakfast.
Do not drink grapefruit juice while taking this medication, as your blood pressure may drop too low. Drinking alcohol may cause a drop in blood pressure when standing up.
Avoid salty foods (containing high amounts of sodium chloride), as they may reduce the blood pressure-lowering effect of Vivace.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
Pregnancy
Your doctor will usually advise you to stop taking Vivace before becoming pregnant or as soon as you know you are pregnant, and will recommend an alternative medication instead of Vivace. Vivace is not recommended at the start of pregnancy, and should not be taken if you are pregnant for more than 3 months, as it may cause serious harm to your baby if used during this period.
Breastfeeding
Vivace is not recommended for breastfeeding mothers, and your doctor should choose an alternative treatment if you wish to continue breastfeeding, especially if your baby is newborn or premature.
Driving and using machines
It is unlikely that Vivace will affect your ability to drive or use machines. However, it may occasionally cause dizziness due to a decrease in blood pressure. If this happens, you should consult your doctor before attempting these activities.
Vivace contains lactose and a coloring agent
If your doctor has told you that you have an intolerance to certain sugars, consult them before taking this medication.
The coloring agent E-110 may cause allergic reactions.
Follow the administration instructions for Vivace exactly as indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.
The recommended doseof Vivace is one tablet per day.
Dose reduction
If you are over 65 years old or have kidney or liver problems, your doctor may prescribe a lower dose.
Administration
Vivace should be taken in the morning after breakfast. The tablet should be swallowed whole with sufficient water. You should try to take your daily dose at approximately the same time each day.
The tablet can be divided into equal doses.
Duration of treatment
It is important that you continue taking Vivace until your doctor tells you to stop.
Please take the exact dose prescribed by your doctor and do not change it without consulting them first.
Use in children and adolescents
Do not give Vivace to children or adolescents under 18 years of age (see section 2, "What you need to know before taking Vivace - Do not take Vivace").
If you take more Vivace than you should
If you have taken more tablets than you should, consult your doctor immediately, as this may cause your blood pressure to drop too low.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately, or go to a medical center or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
If you forget to take Vivace
If you forget to take a dose, take the next dose as you normally would. Do not take a double dose to make up for forgotten doses.
If you stop taking Vivace
It is important that you continue taking Vivace until your doctor tells you to stop.
If you have any further questions about the use of this product, ask your doctor or pharmacist.
Like all medicines, Vivace can cause adverse effects, although not all people suffer from them.
If adverse effects appear, they are usually mild and transient. However, some adverse effects can be serious and require medical attention.
The frequency of adverse effects is classified into the following categories:
Very frequent | At least 1 in 10 patients |
Frequent | At least 1 in 100 patients, but less than 1 in 10 patients |
Infrequent | At least 1 in 1,000 patients, but less than 1 in 100 patients |
Rare | At least 1 in 10,000 patients, but less than 1 in 1,000 patients |
Very rare | Less than 1 in 10,000 patients, including isolated cases |
Unknown | Frequency cannot be estimated with available data |
Frequent Adverse Effects:
Most frequent adverse effects:
Cough, fluid accumulation in tissues causing edema, headache
Other frequent adverse effects:
Decrease in the number of white blood cells, feeling of apathy, balance disorder, sensation of abnormal movement, sensation of vertigo, dizziness, palpitations, hypotension (especially when standing), hot flashes, bronchitis, nausea, abdominal pain, digestive disorders, fatigue, alteration of analytical parameters (e.g., changes indicating abnormal liver function, increased potassium levels).
Infrequent Adverse Effects:
Anemia due to a lack or insufficient number of new blood cells produced by the bone marrow, significant decrease in the number of white blood cells, which increases the likelihood of infection, decrease in the number of blood platelets, which increases the risk of bleeding or bruising, decrease in the number of certain white blood cells, which increases the likelihood of infection, decrease in blood plasma and red blood cell volume ratio, loss of appetite, confusion, insomnia, mood changes, nervousness, anxiety, irritability, altered taste, blurred vision, increased heart rate, fainting (syncope), breathing difficulties, inflammation of the sinuses and nasal mucosa (e.g., constant nasal secretion), sore throat, vomiting, diarrhea, constipation, dry mouth, formation of stones in the bile ducts (especially if there is inflammation of the gallbladder), redness, itching, skin inflammation with redness and itching (eczema), excessive sweating, muscle and joint stiffness, pain in the arms and legs, kidney failure, high protein levels in the urine, inability to achieve or maintain an erection (impotence), feeling of weakness, general malaise, alteration of analytical parameters (e.g., changes indicating abnormal liver function).
Rare Adverse Effects:
Allergic reactions, decreased libido, somnolence, myocardial infarction, cardiac rhythm disorders, chest pain due to lack of oxygen to the heart (angina pectoris), chest pain, stroke, stomach pain, urticaria, abnormal skin redness, muscle cramps, acute kidney failure, accumulation of urea (a waste product excreted in the urine) in the blood, irritability, alteration of analytical parameters (e.g., increased bilirubin, changes indicating abnormal heart or muscle function).
Rare reactions that may be caused by these types of medications include inflammation of the face, lips, tongue, throat, or difficulty breathing. If you notice any of these reactions during treatment, stop taking Vivace and inform your doctor immediately.
Very Rare Adverse Effects (including isolated cases):
Anemia due to rapid destruction of red blood cells, in patients with pre-existing angina pectoris (chest pain due to lack of oxygen to the heart), the frequency, duration, and severity of angina attacks and the occurrence of heart attacks may increase, poor blood circulation that causes fingers and toes to become numb and pale (Raynaud's disease), breathing difficulties, pancreatitis, intestinal obstruction, tongue inflammation, appearance of blisters on the face, mouth, eyes, and genitals along with fever (Stevens-Johnson syndrome), hair loss, psoriasis.
Adverse Effects of Unknown Frequency:
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect that is not listed in this prospectus. You can also report them directly through the national reporting system included in the Spanish Pharmacovigilance System for Human Use Medicines https://www.notificaram.es.
By reporting adverse effects, you can contribute to providing more information on the safety of this medication.
Medicines should not be thrown away through drains or into the trash. Deposit the packaging and unused medications at the SIGRE point in the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and unused medications. This way, you will help protect the environment.
Composition of Vivace
Vivace is a combination of two active substances, delapril hydrochloride and manidipine hydrochloride.
Each Vivace 30 mg/10 mg tablet contains 30 mg of delapril hydrochloride and 10 mg of manidipine hydrochloride, respectively.
The other components are lactose monohydrate, low-substituted hydroxypropylcellulose, hydroxypropylcellulose, magnesium stearate, riboflavin, and aluminum lake E-110 (orange-yellow).
Appearance of the Product and Packaging Content
Vivace is presented in Alu-Alu blisters.
Each Vivace packaging contains 28 scored, round, salmon-colored tablets.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder:
CHIESI ESPAÑA, S.A.U.
Plaça d’Europa, 41-43, Planta 10
08908 L'Hospitalet de Llobregat - Barcelona (Spain)
Manufacturer:
Chiesi Farmaceutici, S.p.A.
Via San Leonardo 96
43122 Parma (Italy)
Or
Fine Foods & Pharmaceuticals N.T.M. S.p.A.
Via Grignano, 43
24041 Brembate (BG)
Italy
This medication is authorized in the following EEA Member States under the following names:
Italy: | Adaptus |
Greece: | Vivace |
Spain: | Vivace |
Date of the Last Revision of this Prospectus: July 2024
Delapril and manidipine are licensed from Takeda Pharmaceutical Company Ltd.
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es.
The average price of VIVACE 30 mg/10 mg TABLETS in October, 2025 is around 21.07 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.