Olmesartan medoxomil 40 mg film-coated tablets
Olmesartan medoxomil
Read this leaflet carefully before you start taking this medicine, as it contains important information for you.
1. What is olmesartan medoxomil and what is it used for
2. What you need to know before you start taking olmesartan medoxomil
3. How to take olmesartan medoxomil
4. Possible side effects
5. Storage of olmesartan medoxomil
6. Contents of the pack and additional information
olmesartán cinfa is used to treat high blood pressure (also known as hypertension)in adults, and in children and adolescents from 6 years of age to less than 18 years of age.High blood pressure can damage blood vessels in organs such as the heart, kidneys, brain, and eyes.In some cases, this can lead to a heart attack, heart failure, or kidney failure, stroke, or blindness.High blood pressure usually does not present symptoms. It is essential to control your blood pressure to prevent damage.
High blood pressure can be controlled with medicines like olmesartán cinfa. Your doctorprobably also recommended that you make some lifestyle changes to help lower your blood pressure (for example, losing weight, quitting smoking, reducing the amount of alcohol you drink, and reducing the amount of salt in your diet).Your doctor may also recommend that you exercise regularly, such as walking or swimming.It is essential to follow your doctor's advice.
Consult your doctor or pharmacist before starting to take olmesartan cinfa.
Tell your doctorif you are taking any of the following medications used to treat high blood pressure (hypertension):
Your doctor may monitor your kidney function, blood pressure, and electrolyte levels (such as potassium) at regular intervals.
See also the information under the heading “Do not take olmesartan cinfa”.
Tell your doctorif you have any of the following health problems:
Consult your doctor if you experience abdominal pain, nausea, vomiting, or diarrhea after taking olmesartan. Your doctor will decide whether to continue treatment. Do not stop taking olmesartan on your own.
Contact your doctor if you experience severe, persistent diarrhea, and significant weight loss. Your doctor will evaluate your symptoms and decide how to proceed with your blood pressure treatment.
As with any other medication that lowers blood pressure, excessive lowering of blood pressure in patients with heart or brain blood flow abnormalities can cause a heart attack or stroke. Therefore, your doctor will carefully monitor your blood pressure.
Inform your doctor if you are pregnant or think you may be pregnant. Olmesartan is not recommended for use at the beginning of pregnancy, and it should not be taken if you are more than 3 months pregnant, as it may cause serious harm to your baby if used during this period (see Pregnancy section).
As with other similar medications, the blood pressure-lowering effect of olmesartan is somewhat less in black patients.
If you are 65 years or older and your doctor decides to increase your olmesartan medoxomilo dose to 40 mg per day, your doctor will regularly monitor your blood pressure to ensure it does not decrease too much.
Olmesartan has been studied in children and adolescents. For more information, consult your doctor. Olmesartan is not recommended for children aged 1 to less than 6 years, and it should not be used in children under 1 year, as there is no experience.
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Particularly, inform your doctor or pharmacist about any of the following medications:
Olmesartan can be taken with or without food.
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
Inform your doctor if you are pregnant or think you may be pregnant. Your doctor will advise you to stop taking olmesartan as soon as you know you are pregnant and to take another medication instead. Olmesartan is not recommended for use at the beginning of pregnancy, and it should not be taken if you are more than 3 months pregnant, as it may cause serious harm to your baby if used during this period (see Pregnancy section).
Inform your doctor if you are breastfeeding or plan to start breastfeeding. Olmesartan is not recommended for breastfeeding mothers, and your doctor may choose another treatment if you wish to breastfeed, especially if your baby is newborn or premature.
You may feel drowsy or dizzy during high blood pressure treatment. If this happens, do not drive or operate machinery until the symptoms have disappeared. Consult your doctor.
This medication contains lactose. If your doctor has told you that you have a certain sugar intolerance, consult with them before taking this medication.
The recommended initial dose is 1 olmesartan 10 mg tablet per day. If blood pressure is not adequately controlled, your doctor may increase the dose up to 20 mg or 40 mg per day or prescribe additional treatment.
Inpatients with mild to moderate renal insufficiencythe maximum dose is 20 mg once a day.
Tablets can be taken with or without food. Take the tablets with a sufficient amount of water (for example, a glass). If possible, take your dose at the same time every day, for example, at breakfast time.
The tablet can be split into equal doses.
Use in children and adolescents aged 6 to under 18 years
The recommended initial dose is 10 mg per day. If the patient's blood pressure is not adequately controlled, the doctor may decide to change the dose up to 20 or 40 mg per day. In children weighing less than 35 kg, the dose will not exceed 20 mg per day.
If you take more olmesartan cinfa than you should
If you take more tablets than necessary or if a child has accidentally ingested tablets.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or callthe Toxicological Information Service,phone 91 562 04 20, indicating the medication and the amount ingested.
If you forget to take olmesartan cinfa
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 dose.
If you interrupt treatment with olmesartan cinfa
It is essential to continue taking olmesartan, 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.
Like all medicines, this medicine may cause side effects, although not everyone will experience them. If they occur, they are often mild and do not require interrupting treatment.
The following side effects may be serious, although not many people may experience them.
In rare cases (affecting up to 1 in 1,000 people), the following allergic reactions have been reported, which can affect the entire body: inflammation of the face, mouth, and/or larynx, along with itching and skin rash.If this happens, stop taking olmesartan and consult your doctor immediately.
Very rarely (but slightly more often in elderly patients) olmesartan may cause a pronounced drop in blood pressure in susceptible patients or as a result of an allergic reaction. This can cause severe dizziness or fainting.If this happens, stop taking olmesartan, consult your doctor immediately, and remain lying down in a horizontal position.
Frequency unknown: If you experience yellowing of the whites of the eyes, dark urine, skin itching, even if you started treatment with olmesartan some time ago,contact your doctor immediatelywho will evaluate your symptoms and decide how to continue treatment for high blood pressure.
These are other side effects known so far with olmesartan:
Frequent side effects (may affect up to 1 in 10 people):
Dizziness, headache, nausea, indigestion, diarrhea, stomach pain, gastroenteritis, fatigue, sore throat,nasal congestion and discharge, bronchitis, flu-like symptoms, cough, chest pain,back pain, bone pain, joint pain, urinary tract infection, swelling ofankles, feet, legs, hands, arms, blood in urine.
Some changes have also been observed in the results of certain blood tests:increase in triglyceride levels (hypertriglyceridemia), increase in uric acid levels(hyperuricemia), increase in urea in the blood, increases in liver and muscle function tests.
Rare side effects (may affect up to 1 in 100 people):
Severe allergic reactions that can affect the entire body and may cause breathing problems, as well as a rapid drop in blood pressure that can even lead to fainting (anaphylactic reactions), facial inflammation, dizziness, vomiting, weakness, feeling unwell, muscle pain, skin rash, allergic skin rash, itching, hives, angina (chest pain or discomfort).
In blood tests, a decrease in the number of a type of blood cell called platelets (thrombocytopenia) has been observed.
Rare side effects (may affect up to 1 in 1,000 people):
Lack of energy, muscle cramps, worsening of kidney function, kidney failure.
Intestinal angioedema: swelling in the intestine that presents symptoms such as abdominal pain, nausea, vomiting, and diarrhea.
Some changes have been observed in the results of certain blood tests. These include an increase in potassium levels in the blood (hyperkalemia) and an increase in components related to kidney function.
Other side effects in children and adolescents:
Side effects similar to those reported in adults have been observed in children. However, dizziness and headache have been observed more frequently in children, and nosebleeds are a frequent side effect observed only in children.
Reporting side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it ispossible side effects that do not appear in this prospectus. You can also report themdirectly through the Spanish System for Pharmacovigilance of Medicines for Human Use: https://www.notificaram.es.By reporting side effects, you can contribute toproviding more information about 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/container/label after CAD. The expiration date is the last day of the month indicated.
This medication does not require special storage conditions.
Medications 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.
Composition of olmesartan cinfa
Each film-coated tablet contains 40 mg of olmesartan medoxomilo.
Tablet core:microcrystalline cellulose, lactose monohydrate, povidone, hydroxypropyl cellulose, and magnesium stearate.
Tablet coating:Opadry Y-1-7000 (hypromellose, titanium dioxide, and macrogol).
Appearance of the product and contents of the packaging
Olmesartan cinfa 40 mg are film-coated tablets, oblong, white, biconvex, scored on one face and marked with the code OL4 on the other face.
They are presented in blister packs with 28 film-coated tablets.
Holder of the marketing authorization and responsible manufacturer
Cinfa Laboratories, S.A.
Carretera Olaz-Chipi, 10. Industrial Estate Areta
31620 Huarte (Navarra) - Spain
Date of the last review of this leaflet: February 2025
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/
You can access detailed and updated information about this medicine by scanning with your smartphone the QR code included in the leaflet and packaging. You can also access this information at the following internet address:https://cima.aemps.es/cima/dochtml/p/79898/P_79898.html
QR code to:https://cima.aemps.es/cima/dochtml/p/79898/P_79898.html
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