Leaflet: information for the user
CAPENON HCT 20 mg/5 mg/12,5 mg film-coated tablets
Olmesartan medoxomil / Amlodipine / Hydrochlorothiazide
Read this leaflet carefully before you start to take this medicine, because it contains important information for you.
-Keep this leaflet, as you may need to read it again.
-If you have any questions, consult your doctor or pharmacist.
-This medicine has been prescribed for you only, and you must not give it to others even if they have the same symptoms 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 section 4.
Contents of the pack and additional information
Capenon HCT contains three active ingredients called olmesartan medoxomil, amlodipine (as amlodipine besylate) and hydrochlorothiazide. The three ingredients help control high blood pressure.
The action of these ingredients contributes to lowering blood pressure.
Capenon HCT is used to treat high blood pressure:
If you think you may be allergic, inform your doctor before taking Capenon HCT.
Do not take Capenon HCT if any of these cases occur.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Capenon HCT.
Tell your doctorif you are taking any of the following medications used to treat high blood pressure (hypertension):
Your doctor may monitor your renal function, blood pressure, and 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:
See 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.
Like any other medication that lowers blood pressure, excessive blood pressure reduction in patients with heart or brain blood flow alterations can cause a heart attack or stroke. Therefore, your doctor will closely monitor your blood pressure.
Capenon HCT may cause an increase in lipid and uric acid levels in your blood. Your doctor will likely want to perform blood tests from time to time to monitor these possible changes.
You may experience changes in the levels of certain chemicals in your blood called electrolytes. Your doctor will likely want to perform blood tests from time to time to monitor this possible change. Some signs of electrolyte changes are: thirst, dry mouth, muscle pain or cramps, tired muscles, low blood pressure (hypotension), feeling weak, slow, tired, drowsy, or restless, nausea, vomiting, decreased need to urinate, rapid heart rate.Tell your doctor if you notice any of these symptoms.
If you are undergoing parathyroid function tests, stop taking Capenon HCT before the tests are performed.
It is reported to athletes that this medication contains a component that can result in a positive analytical control for doping as positive.
Inform your doctor if you are pregnant (or think you may be). Do not recommend the use of Capenon HCT at the beginning of pregnancy, and do not take it if you are more than 3 months pregnant, as it can cause severe damage to your baby if taken during this stage (see the section “Pregnancy and breastfeeding”).
Children and adolescents (under 18 years)
Do not recommend the use of Capenon HCT in children and adolescents under 18 years.
Use of Capenon HCT with other medications:
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to takeany of the following medications:
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”).
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any of the following medications for:
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
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 may cause an increase in the levels of the active ingredient amlodipine in your blood, which may cause an unpredictable increase in the effect of lowering blood pressure of Capenon HCT.
Be careful when drinking alcohol while taking Capenon HCT, as some people may feel dizzy, nauseous, or experience headaches. If this happens, do not drink any alcohol.
Older patients
If you are over 65 years old, your doctor will regularly monitor your blood pressure every time you increase the dose, to ensure that your blood pressure does not drop too low.
Pregnancy and breastfeeding:
Pregnancy
Inform your doctor if you are pregnant, or if you think you may be. Your doctor will advise you to stop taking Capenon HCT before becoming pregnant or as soon as you know you are pregnant, and will advise you to take another medication instead of Capenon HCT. Do not recommend the use of Capenon HCT during pregnancy, and do not take it if you are more than 3 months pregnant, as it may cause severe damage to your baby if used from the third month of pregnancy.
If you become pregnant while taking Capenon HCT, inform and see your doctor immediately.
Breastfeeding
Inform your doctor if you are breastfeeding or planning to start breastfeeding. It has been shown that amlodipine and hydrochlorothiazide pass into breast milk in small amounts. Do not recommend Capenon HCT in mothers who are breastfeeding, and your doctor may choose another treatment if you want to breastfeed.
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.
Driving and operating machinery:
You may feel drowsy, nauseous, or experience headaches while taking medication for high blood pressure. If this happens, do not drive or operate machinery until the symptoms have disappeared. Consult your doctor.
This medication contains less than 1 mmol of sodium (23 mg) per coated tablet; it is essentially “sodium-free”.
Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. If in 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 are likely to experience a drop in blood pressure, accompanied by symptoms such as dizziness, and a rapid or slow heart rate.
If you take more tablets than you should or if a child accidentally ingests some tablets, contact your doctor immediately or go to the nearest emergency center and bring the medication packaging or this leaflet with you.
Excess fluid may accumulate in the lungs (pulmonary edema) causing difficulty breathing that may develop up to 24-48 hours after ingestion.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological 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 missed doses.
If you interrupt treatment with Capenon HCT:
It is essential to continue taking Capenon HCT, unless your doctor tells you to stop treatment.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
The following side effects can be serious, although they may 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, stop taking Capenon HCT and consult your doctor immediately..
Capenon HCT can cause a pronounced drop in blood pressure in susceptible patients. This can cause severe dizziness or fainting.If this happens, stop taking Capenon HCT, consult your doctor immediately, and remain lying down in a horizontal position.
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 known side effects of 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 experience side effects, they have been classified as frequent, infrequent, rare, and very rare.
These are other side effects known so far with Capenon HCT:
If these side effects occur, they are often mild andit 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, joint swelling, sensation of urgency to urinate, weakness, ankle swelling, fatigue, abnormal laboratory test results.
Infrequent
(may affect up to 1 in 100 people)
Dizziness when getting up, vertigo, rapid heartbeat, sensation of fainting, flushing and sensation 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, stomach burning, stomach discomfort, flatulence, joint or bone pain, back pain, bone pain, blood in urine, flu-like symptoms, chest pain, pain.
Infrequent
(may affect up to 1 in 100 people)
Reduction in the number of a type of blood cell called platelets, which can cause easy bruising or prolong bleeding time, anaphylactic reactions, abnormal decrease in appetite (anorexia), sleep problems, irritability, mood changes including anxiety, sensation of depression, chills, sleep disorders, alteration of taste, loss of consciousness, decrease in sense of touch, sensation of numbness, worsening of myopia, ringing in the ears (tinnitus), angina (pain or unpleasant sensation in the chest, known as angina pectoris), irregular heartbeat, rash, hair loss, allergic skin inflammation, skin redness, purple patches or spots on the skin due to small hemorrhages (purpura), skin discoloration, red itchy patches (urticaria), increased sweating, pruritus, skin rash, skin reactions to light, such as sunburn or skin eruption, muscle pain, urination problems, sensation of needing to urinate at night, increased breast size in men, decreased libido, facial swelling, sensation of discomfort, weight gain or loss, fatigue.
Rare
(may affect up to 1 in 1,000 people)
Salivary gland inflammation and pain, 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, sensation 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, yellowish discoloration 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 eruption, urticaria, skin redness, severe itching, blisters, skin peeling and inflammation, inflammation of mucous membranes (Stevens-Johnson syndrome, toxic epidermal necrolysis), sometimes very severe, movement impairment, acute kidney failure, non-infectious kidney inflammation, kidney function decrease, fever, intestinal angioedema: swelling in the intestine accompanied by 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.
Unknown frequency side effects
(cannot be estimated from available data)
Decreased vision or eye pain (possible signs of fluid accumulation in the vascular layer of the eye (choroidal hemorrhage) or acute angle-closure glaucoma).
Tremors, rigid posture, mask-like face, slow movements, and unsteady gait with dragging feet.
Skin and lip cancer (non-melanoma skin cancer).
Reporting 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 System for the Vigilance of Medicines for Human Use:www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging and blister after“CAD.”.The expiration date is the last day of the month indicated.
No special storage conditions are required.
Medicines should not be disposed of through drains or in the trash. Dispose of the packaging and unused medications at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of unused packaging and medications. By doing so, you will help protect the environment.
The active principles 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 cornstarch, silica gel microcrystalline cellulose (microcrystalline cellulose with anhydrous colloidal silicon dioxide), croscarmellose sodium and magnesium stearate.
Tablet coating: Poly(vinyl alcohol), macrogol 3350, talc, titanium dioxide (E-171), yellow iron oxide (E-172), red iron oxide (E-172) and black iron oxide (E-172).
Appearance of the product and contents of the package
Capenon HCT 20 mg/5 mg/12.5 mg film-coated tablets are orange-colored, round tablets of 8 mm in diameter, with the inscription “C51” on one face.
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, Ground floor left
28223 Pozuelo de Alarcón - Madrid
Responsible for manufacturing
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 medicine 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
Last review date of this leaflet: January 2025.
Other sources of information
The detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/.
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