


Ask a doctor about a prescription for CAPENON HCT 20 mg/5 mg/12.5 mg FILM-COATED TABLETS
Package Leaflet: Information for the User
CAPENON HCT 20 mg/5 mg/12.5 mg film-coated tablets
Olmesartan medoxomil / Amlodipine / Hydrochlorothiazide
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.
Contents of the pack and other information
Contents of the pack and further information
Capenon HCT contains three active substances called olmesartan medoxomil, amlodipine (as amlodipine besylate) and hydrochlorothiazide. These three substances help to control high blood pressure.
The action of these substances contributes to lowering your blood pressure.
Capenon HCT is used to treat high blood pressure:
Do not take Capenon HCT:
If you think you may be allergic, inform your doctor before taking Capenon HCT.
Do not take Capenon HCT if any of these apply to you.
Warnings and precautions
Consult your doctor or pharmacist before starting Capenon HCT.
Tell your doctorif you are taking any of the following medicines used to treat high blood pressure (hypertension):
Your doctor may need to check 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 Capenon HCT”.
Tell your doctorif you have any of the following health problems:
Contact your doctorif you experience any of the following symptoms:
Consult your doctor if you experience abdominal pain, nausea, vomiting, or diarrhea after taking Capenon HCT. Your doctor will decide whether to continue treatment. Do not stop taking Capenon HCT on your own.
As with any other medicine that lowers blood pressure, excessive lowering of blood pressure in patients with impaired blood flow to the heart or brain may cause a heart attack or stroke. Therefore, your doctor will carefully monitor your blood pressure.
Capenon HCT may cause an increase in lipid and uric acid levels in the blood. Your doctor will likely want to perform a blood test from time to time to monitor these potential changes.
A change in blood levels of certain chemicals called electrolytes may occur. Your doctor will likely want to perform a blood test from time to time to monitor this potential change. Some signs of electrolyte changes are: thirst, dry mouth, muscle pain or cramps, tired muscles, low blood pressure (hypotension), feeling of weakness, slowness, fatigue, drowsiness or restlessness, nausea, vomiting, decreased need to urinate, rapid heartbeat. Tell your doctor if you notice any of these symptoms.
If you are going to have parathyroid function tests, you must stop taking Capenon HCT before these tests are performed.
Athletes are informed that this medicine contains a component that may result in a positive doping test.
You must inform your doctor if you are pregnant (or think you might be). It is not recommended to use Capenon HCT at the start of pregnancy, and it must not be taken if you are more than 3 months pregnant, as it may cause serious harm to your baby if taken at this stage (see section “Pregnancy and breast-feeding”).
Children and adolescents (under 18 years):
The use of Capenon HCT is not recommended in children and adolescents under 18 years.
Using Capenon HCT with other medicines:
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, including:
Your doctor may need to adjust 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 Capenon HCT” and “Warnings and precautions”).
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines for:
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicine.
Taking Capenon HCT with food and drinks:
Capenon HCT can be taken with or without food.
People taking Capenon HCT should not consume grapefruit or grapefruit juice. This is because grapefruit and grapefruit juice can lead to an increase in the levels of the active ingredient amlodipine in the blood, which may cause an unpredictable increase in the blood pressure-lowering effect of Capenon HCT.
Be careful when drinking alcohol while taking Capenon HCT, as some people feel faint or dizzy. If this happens, do not drink any alcohol.
Elderly patients:
If you are over 65 years old, your doctor will regularly check your blood pressure whenever your dose is increased, to ensure that your blood pressure does not drop too much.
Pregnancy and breast-feeding:
Pregnancy
You must inform your doctor if you are pregnant (or think you might be). Your doctor will advise you to stop taking Capenon HCT before you become pregnant or as soon as you know you are pregnant, and will advise you to take a different medicine instead of Capenon HCT. It is not recommended to use Capenon HCT during pregnancy, and it must not be taken when you are more than 3 months pregnant, as it may cause serious harm to your baby if taken from the third month of pregnancy onwards.
If you become pregnant while taking Capenon HCT, inform and consult your doctor immediately.
Breast-feeding
Tell your doctor if you are breast-feeding or about to start breast-feeding. It has been shown that amlodipine and hydrochlorothiazide pass into breast milk in small amounts. Capenon HCT is not recommended for mothers who are breast-feeding, and your doctor may choose a different treatment if you wish to breast-feed.
If you are pregnant or breast-feeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Driving and using machines:
You may feel drowsy, sick, or dizzy, or have a headache while being treated for high blood pressure. If this happens, do not drive or use machines until the symptoms have disappeared. Consult your doctor.
This medicine contains less than 1 mmol sodium (23 mg) per film-coated tablet, which is essentially “sodium-free”.
Follow exactly the administration instructions of this medication indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
If you take more Capenon HCT than you should:
If you take more tablets than you should, you will probably suffer from a drop in blood pressure, accompanied by symptoms such as dizziness, and rapid or slow heartbeat.
If you take more tablets than you should or if a child accidentally ingests some tablets, contact your doctor or go to the nearest emergency center immediately and bring the medication package or this leaflet with you.
Excess fluid may accumulate in the lungs (pulmonary edema) causing difficulty breathing that can develop up to 24-48 hours after ingestion.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20.
If you forget to take Capenon HCT:
If you forget to take a dose, take the usual dose the next day. Do not take a double dose to make up for the forgotten doses.
If you interrupt treatment with Capenon HCT:
It is important to continue taking Capenon HCT, unless your doctor tells you to interrupt treatment.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication can produce side effects, although not all people suffer from them. If they occur, they are often mild and do not require interrupting treatment.
The following side effects may be serious, although they affect only a small group of people:
During treatment with Capenon HCT, allergic reactions with inflammation of the face, mouth, and/or larynx (vocal cords), along with itching and skin rash, may occur. If this happens to you, stop taking Capenon HCT and consult your doctor immediately.
Capenon HCT may produce a pronounced drop in blood pressure in susceptible patients. This can cause fainting or severe dizziness. If this happens to you, stop taking Capenon HCT, consult your doctor immediately, and remain lying down in a horizontal position.
Frequency not known: If you experience yellowing of the whites of the eyes, dark urine, itching of the skin, even if you started treatment with Capenon HCT a long time ago, contact your doctor immediatelywho will evaluate your symptoms and decide how to continue treatment for blood pressure.
Capenon HCT is a combination of three active substances. The following information, first, describes the side effects reported so far with the combination Capenon HCT (in addition to those already mentioned) and, second, the side effects known for each of the active substances separately, or when two of the substances are taken together.
To give you an idea of the number of patients who may have side effects, they have been classified as frequent, uncommon, rare, and very rare.
These are other known side effects with Capenon HCT:
If these effects occur, they are often mild and it is not necessary to interrupt treatment.
Frequent
(may affect up to 1 in 10 people)
Upper respiratory tract infection, sore throat and nose, urinary tract infection, dizziness, headache, perception of heartbeats, low blood pressure, nausea, diarrhea, constipation, cramps, swelling of the joints, urge to urinate, weakness, swelling of the ankles, fatigue, abnormal laboratory test values.
Uncommon
(may affect up to 1 in 100 people)
Dizziness when standing up, vertigo, rapid heartbeat, feeling of fainting, flushing and feeling of heat in the face, cough, dry mouth, muscle weakness, inability to have or maintain an erection.
These are the side effects known for each of the active substances separately or when two of the substances are taken together:
They may be side effects due to Capenon HCT, even if they have not been observed so far with Capenon HCT.
Very frequent
(may affect more than 1 in 10 people)
Edema (fluid retention).
Frequent
(may affect up to 1 in 10 people)
Bronchitis, stomach and intestine infection, vomiting, increased blood sugar, sugar in urine, confusion, drowsiness, visual disturbances (including double vision and blurred vision), nasal secretion or congestion, sore throat, difficulty breathing, cough, abdominal pain, heartburn, stomach discomfort, flatulence, joint or bone pain, back pain, bone pain, blood in urine, flu-like symptoms, chest pain, pain.
Uncommon
(may affect up to 1 in 100 people)
Reduction in the number of a type of blood cells called platelets, which can cause easy bruising or prolonged bleeding time, anaphylactic reactions, abnormal decrease in appetite (anorexia), sleep problems, irritability, mood changes including anxiety, feeling of depression, chills, sleep disorders, alteration of the sense of taste, loss of consciousness, decrease in the sense of touch, feeling of tingling, worsening of myopia, ringing in the ears (tinnitus), angina (pain or unpleasant sensation in the chest, known as angina pectoris), irregular heartbeats, rash, hair loss, allergic skin inflammation, skin redness, purple spots or patches on the skin due to small hemorrhages (purpura), skin discoloration, red itchy hives (urticaria), increased sweating, itching, skin rash, skin reactions to light, such as sunburn or skin rash, muscle pain, urination problems, feeling of needing to urinate at night, increase in breast size in men, decrease in sexual desire, facial swelling, feeling of discomfort, weight gain or loss, exhaustion.
Rare
(may affect up to 1 in 1,000 people)
Inflammation and pain of the salivary glands, decrease in the number of white blood cells in the blood, which could increase the risk of infections, decrease in the number of red blood cells (anemia), bone marrow damage, restlessness, feeling of loss of interest (apathy), seizures (convulsions), yellowish perception of objects when looking at them, dry eyes, blood clots (thrombosis, embolism), fluid accumulation in the lungs, pneumonia, inflammation of blood vessels and small blood vessels in the skin, pancreatitis, yellowing of the skin and eyes, acute inflammation of the gallbladder, symptoms of lupus erythematosus such as skin rash, joint pain, and cold hands and fingers, severe skin reactions including intense skin rash, urticaria, skin redness of the body, severe itching, blisters, peeling, and skin inflammation, inflammation of the mucous membranes (Stevens-Johnson syndrome, toxic epidermal necrolysis), sometimes very severe, deterioration of movement, acute kidney failure, non-infectious inflammation of the kidney, decrease in kidney function, fever, intestinal angioedema: swelling in the intestine that occurs with symptoms such as abdominal pain, nausea, vomiting, and diarrhea.
Very rare
(may affect up to 1 in 10,000 people)
High muscle tension, numbness of hands or feet, heart attack, stomach inflammation, gum thickening, intestinal obstruction, liver inflammation.
Acute difficulty breathing (signs include severe difficulty breathing, fever, weakness, and confusion).
Side effects of unknown frequency
(cannot be estimated from the available data)
Decreased vision or eye pain (possible signs of fluid accumulation in the vascular layer of the eye (choroidal effusion) or acute angle-closure glaucoma).
Tremors, rigid posture, mask-like face, slow movements, and unsteady gait.
Skin and lip cancer (non-melanoma skin cancer).
Reporting of side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of sight and reach of children.
Do not use this medication after the expiration date that appears on the package and blister after "EXP.". The expiration date is the last day of the month indicated.
No special storage conditions are required.
Medications should not be thrown down the drain or into the trash. Deposit the packages and medications you no longer need in the SIGRE Point of the pharmacy. If in doubt, ask your pharmacist how to dispose of the packages and medications you no longer need. This way, you will help protect the environment.
Composition of Capenon HCT
The active ingredients are olmesartan medoxomil, amlodipine (as amlodipine besylate), and hydrochlorothiazide.
Each film-coated tablet contains 20 mg of olmesartan medoxomil, 5 mg of amlodipine (as amlodipine besylate), and 12.5 mg of hydrochlorothiazide.
The other components are:
Tablet core: Pregelatinized corn starch, silified microcrystalline cellulose (microcrystalline cellulose with anhydrous colloidal silicon dioxide), sodium croscarmellose, and magnesium stearate.
Tablet coating: Poly(vinyl alcohol), macrogol 3350, talc, titanium dioxide (E-171), iron oxide (III) yellow (E-172), iron oxide (III) red (E-172), and iron oxide (II, III) black (E-172).
Appearance of the product and package contents
Capenon HCT 20 mg/5 mg/12.5 mg film-coated tablets are light orange, round tablets of 8 mm, with the inscription "C51" on one side.
Capenon HCT film-coated tablets are presented:
Not all packages are marketed.
Marketing authorization holder
Daiichi Sankyo España, S.A.
Paseo del Club Deportivo nº1,
Edificio 14, Planta baja izquierda
28223 Pozuelo de Alarcón - Madrid
Manufacturer
Daiichi Sankyo Europe GmbH
Luitpoldstrasse 1
85276 Pfaffenhofen
Germany
or
Berlin-Chemie AG
Glienicker Weg 125
12489 Berlin
Germany
or
Menarini – Von Heyden GmbH
Leipziger Strasse 7-13
01097 Dresden
Germany
This medication is authorized in the Member States of the European Economic Area with the following names:
Italy: Giantrix 20 mg/5 mg/12.5 mg
Netherlands: Capenon HCT 20 mg/5 mg/12.5 mg
Spain: Capenon HCT 20 mg/5 mg/12.5 mg
Date of the last revision of this leaflet: January 2025.
Other sources of information
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 CAPENON HCT 20 mg/5 mg/12.5 mg FILM-COATED TABLETS in November, 2025 is around 15.52 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.
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for CAPENON HCT 20 mg/5 mg/12.5 mg FILM-COATED TABLETS – subject to medical assessment and local rules.