Package Leaflet: Information for the User
Irbesartan Cinfa 75 mg Tablets EFG
Read this leaflet carefully before you start taking this medicine because it contains important information for you.
irbesartan cinfabelongs to a group of medicines known as angiotensin-II receptor antagonists. Angiotensin-II is a substance produced in the body that binds to receptors, causing blood vessels to constrict. This results in an increase in blood pressure.Irbesartanprevents angiotensin-II from binding to these receptors, relaxing blood vessels and reducing blood pressure.Irbesartandelays the deterioration of renal function in patients with high blood pressure and type 2 diabetes.
irbesartan cinfais used in adult patients:
Do not take irbesartan cinfa
Warnings and precautions
Consult your doctor or pharmacist before starting to take irbesartan cinfaandif any of the following aspects affect you:
Your doctor may monitor your renal function, blood pressure, and blood electrolyte levels (such as potassium), at regular intervals.
See also the information under the heading “Do not take irbesartan cinfa”.
Consult your doctor if you experience abdominal pain, nausea, vomiting, or diarrhea after taking irbesartan. Your doctor will decide whether to continue treatment. Do not stop taking irbesartan on your own.
If you are pregnant, if you suspect you may be, orif you plan to become pregnant, inform your doctor. Irbesartan is not recommended for use at the beginning of pregnancy (first 3 months) and should not be administered after the third month of pregnancy, as it may cause serious harm to your baby (see section “Pregnancy”).
Children and adolescents
This medication should not be used in children and adolescents as its safety and efficacy have not been fully established.
Other medications and irbesartan cinfa
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Your doctor may need to adjust your dose and/or take other precautions:
If you are taking a converting enzyme inhibitor (ACEI) or aliskiren (see also the information under the headings “Do not take irbesartan cinfa” and “Warnings and precautions”).
You may need to have blood tests if you are taking:
If you are taking a type of analgesic, known as non-steroidal anti-inflammatory drugs, the effect of irbesartan may be reduced.
Taking irbesartan cinfa with food and drinks
The tablets can be taken with or without food.
Pregnancy and breastfeeding
Pregnancy
Inform your doctor if you are pregnant, if you suspect you may be, or if you plan to become pregnant. Your doctor will usually advise you to stop taking irbesartan before becoming pregnant or as soon as you become pregnant and recommend taking another antihypertensive medication instead. Irbesartan is not recommended for use at the beginning of pregnancy and should not be administered after the third month of pregnancy as it may cause serious harm to your baby when administered from that point onwards.
Breastfeeding
Inform your doctor if you plan to start or are breastfeeding as irbesartan is not recommended for use during this period. Your doctor may decide to administer a more suitable treatment if you want to breastfeed, especially for newborns or premature babies.
Driving and operating machinery
It is unlikely that irbesartan will affect your ability to drive vehicles or operate machinery. However, during hypertension treatment, occasional dizziness or fatigue may occur. If you experience these symptoms, discuss them with your doctor before driving or operating machinery.
Irbesartan cinfa contains lactose.
This medication contains lactose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
Irbesartan cinfa contains hydrogenated ricin oil.
This medication may cause stomach discomfort and diarrhea due to the presence of hydrogenated ricin oil.
Irbesartan cinfa contains sodium.
This medication contains less than 1 mmol of sodium (23 mg) per tablet; it is essentially “sodium-free”.
Method of administration
Irbesartan is administered orally . The tablets should be swallowed with a sufficient amount of liquid (e.g. a glass of water). Irbesartan can be taken with or without food. Try to take your daily dose at the same time every day. It is essential to continue taking this medication until your doctor advises you otherwise.
The usual dose is 150 mg once a day (two tablets a day). Depending on the blood pressure response, this dose may be increased to 300 mg once a day (four tablets a day).
In patients with high blood pressure and type 2 diabetes, the recommended maintenance dose for the treatment of associated kidney impairment is 300 mg once a day (four tablets a day).
Your doctor may recommend a lower dose, especially at the beginning of treatment, in certain patients, such as those undergoing hemodialysis or those over 75 years old .
The maximum blood pressure-lowering effect should be achieved within 4-6 weeks after starting treatment.
Use in children and adolescents
Irbesartan should not be administered to children under 18 years old. If a child swallows several tablets, contact your doctor immediately.
If you take more irbesartan cinfa than you should
If you accidentally take too many tablets, contact your doctor immediately.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
If you forget to take irbesartan cinfa
If you accidentally forget to take a dose, simply take your regular dose when it is due next. Do not take a double dose to compensate for the missed doses.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medicationmay cause side effects, although not everyone will experience them.
However, some of these side effects can be serious and may require medical attention.
Like with similar medications, in rare cases, skin allergic reactions (skin rash, urticaria) have been reported in patients treated with irbesartán, as well as localized inflammation in the face, lips, and/or tongue. If you think you may be having this type of reaction or experience shortness of breath,stop takingirbesartánand seek immediate medical attention.
The side effects mentioned below are grouped by frequency:
Very frequent:may affect more than 1 in 10 patients.
Frequent:may affect up to 1 in 10 patients.
Infrequent:may affect up to 1 in 100 patients.
The side effects reported in clinical trials conducted in patients treated with irbesartán were:
Since the marketing of irbesartán, some side effects have been reported. The side effects observed with unknown frequency (cannot be estimated from available data) are:feeling of spinning, headache, taste alteration, ringing in the ears, muscle cramps, muscle and joint pain,decreased red blood cell count (anemia - symptoms may include fatigue, headaches, difficulty breathing during exercise, dizziness, and paleness),reduced platelet count, abnormal liver function, increased potassium levels in blood, kidney function impairment, and inflammation of small blood vessels, mainly in the skin area (condition known as leukocytoclastic vasculitis),severe allergic reactions (anaphylactic shock) and low blood sugar levels. Cases of rare icterus (yellowing of the skin and/or white of the eyes) have also been observed.With rare frequency: intestinal angioedema: intestinal swelling presenting symptoms such as abdominal pain, nausea, vomiting, and diarrhea.
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 prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicinal Products for Human Use: https://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 the sight and reach of children.
Store in the original packaging to protect it from light.
Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
Medications should not be disposed of through drains or in the trash. Dispose of packaging and medications you no longer need at the SIGRE point of the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of irbesartan cinfa
Appearance of the product and contents of the packaging
White, cylindrical, biconvex tablets marked with the code “Ir7”.
Presented in PVC-PVDC/Aluminum blisters. Each package contains 28 tablets.
Holder of the marketing authorization and responsible manufacturer
Cinfa Laboratories, S.A
Carretera Olaz-Chipi, 10. Areta Industrial Estate
31620 Huarte (Navarra) – Spain
Date of the last review of this leaflet:February 2025
The detailed and updated information on this medication 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 medication by scanning the QR code included in the leaflet and packaging with your smartphone. You can also access this information at the following internet address:https://cima.aemps.es/cima/dochtml/p/70117/P_70117.html
QR code to:https://cima.aemps.es/cima/dochtml/p/70117/P_70117.html
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