PATIENT INFORMATION LEAFLET
CANDESARTAN RANBAXY 32 mg FILM-COATED TABLETS
Candesartan cilexetil
Read this leaflet carefully before you start taking 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, ask your doctor or pharmacist.
- This medicine has been prescribed for you only. Do not pass it on to others even if they have the same symptoms, as it may harm them.
- If you experience any side effects, talk to your doctor or pharmacist, even if they are not listed in this leaflet. See section 4.
1. What Candesartan Ranbaxy is and what it is used for
2. What you need to know before you take Candesartan Ranbaxy
3. How to take Candesartan Ranbaxy
4. Possible side effects
5. Storage of Candesartan Ranbaxy
6. Contents of the pack and additional information
The name of this medication is Candesartán Ranbaxy. The active ingredient is candesartan cilexetilo. It belongs to a group of medications called angiotensin II receptor antagonists. It works by causing the relaxation and widening of blood vessels. This helps to lower your blood pressure. It also makes it easier for your heart to pump blood to all parts of your body.
Candesartán is indicated for:
Do not take Candesartán Ranbaxy
If you are unsure if you are in any of these situations, consult your doctor or pharmacist before taking Candesartán Rambaxy.
Warnings and precautions:
Consult your doctor or pharmacist before starting to take Candesartán Ranbaxy:
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 Candesartán Ranbaxy”.
Consult your doctor if you experience abdominal pain, nausea, vomiting, or diarrhea after taking Candesartan SUN. Your doctor will decide if you should continue treatment. Do not stop taking Candesartan SUN on your own.
You must inform your doctor if you are pregnant (or if you suspect that you may be). Your doctor will usually recommend that you stop taking candesartán as soon as you know you are pregnant and will recommend that you take another medication instead of candesartán. Candesartán should not be used at the beginning of pregnancy, and in no case should it be administered if you are more than three months pregnant, as it may cause serious harm to your baby when administered from that point onwards (see the Pregnancy section).
If you are in any of these situations, your doctor may want to see you more frequently and perform some tests.
If you are to undergo surgery, inform your doctor or dentist that you are taking candesartán. This is because candesartán, in combination with some anesthetics, may cause a drop in blood pressure.
Children and adolescents
Candesartán has been studied in children. For more information, consult your doctor.
Candesartán should not be administered to children under 1 year of age, due to the potential risk to the developing kidneys.
Taking Candesartán Ranbaxy with other medications:
Inform your doctor or pharmacist if you are using or have recently used other medications, including those purchased without a prescription.
Candesartán Ranbaxy may affect how some medications work and some medications may influence the effect of Candesartán Ranbaxy. If you are taking certain medications, your doctor may need to perform blood tests at regular intervals.
Especially, inform your doctor if you are taking any of the following medications:
Your doctor may need to modify your dose and/or take other precautions:
Candesartán Ranbaxy with food and drinks (especially alcohol):
Pregnancy and breastfeeding:
Pregnancy
You must inform your doctor if you are pregnant (or if you suspect that you may be). Your doctor will usually recommend that you stop taking candesartán as soon as you know you are pregnant and will recommend that you take another medication instead of candesartán. Candesartán should not be used at the beginning of pregnancy, and in no case should it be administered if you are more than three months pregnant, as it may cause serious harm to your baby when administered from that point onwards.
Breastfeeding
Inform your doctor if you are breastfeeding or are about to start. Candesartán is not recommended during breastfeeding, and your doctor will choose another treatment for you if you wish to breastfeed, especially if your baby is newborn or premature.
Driving and operating machinery:
Some patients may feel tired or dizzy when taking candesartán. If this happens to you, do not drive or operate tools or machinery.
Candesartán Ranbaxy contains lactose
This medication contains lactose. If your doctorhas indicated that you have a certain sugar intolerance, consult with him before taking this medication.
Follow exactly the administration instructions of this medication as indicated by your doctor. In case of doubt, consult your doctor or pharmacist again. It is essential to continue taking candesartan every day.
You can take candesartan with or without food.
The tablets should be swallowed with the help of water.
Try to take the tablets every day at the same time. This will help you remember to take them.
For dosages that cannot be obtained with Candesartan Ranbaxy tablets, there are other medications that contain other doses of candesartan cilexetil.
Hypertension
The usual dose is 8 mg once a day. The dose may be increased to 16 mg per day and then to 32 mg per day depending on the blood pressure response.
In some patients, such as those with liver problems, kidney problems, or those who have recently lost body fluids, for example, due to vomiting, diarrhea, or because they are taking diuretics, the doctor may prescribe a lower initial dose.
Some patients of black descent may present a reduced response to this type of medication when given as a single treatment, and these patients may need a higher dose.
Use in children and adolescents with high blood pressure:
Children from 6 to <18
The recommended initial dose is 4 mg once a day.
Patients weighing less than 50 kg: In some patients whose blood pressure is not adequately controlled, your doctor may decide to increase the dose up to a maximum of 8 mg once a day.
Patients weighing 50 kg or more: In some patients whose blood pressure is not adequately controlled, your doctor may decide to increase the dose up to a maximum of 8 mg once a day and 16 mg once a day.
Heart failure:
The usual initial dose in heart failure is 4 mg once a day. If necessary, the dose may be doubled in intervals of at least two weeks up to 32 mg once a day. Candesartan can be taken with other medications for the treatment of heart failure, your doctor will decide which treatment is most suitable for you.
If you take more Candesartan Ranbaxy 32 mg than you should
If you have taken more candesartan than prescribed by your doctor, contact your doctor or pharmacist immediately.
In case of overdose or accidental ingestion, consult the Toxicological Information Service. Phone 91 562 04 20, indicating the medication and the amount ingested.
If you forget to take Candesartan Ranbaxy 32 mg
Do not take a double dose to compensate for the missed dose. Simply take the next dose at the usual time.
If you interrupt treatment with Candesartan Ranbaxy 32 mg
If you stop taking candesartan, your blood pressure may increase again. Therefore, do not stop taking candesartan before consulting your doctor.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
It is essential that you know which side effects could occur.
Severe side effects
Stop taking Candesartán Ranbaxy and see your doctor immediately if you experience any of the following allergic reactions:
Candesartán may cause a decrease in white blood cells. Your resistance to infections may decrease, and you may feel tired, have an infection, or fever. If this happens, contact your doctor.
Your doctor may perform a blood test at regular intervals to check if candesartán is affecting your blood (agranulocytosis).
Other side effects:
Frequent (may affect up to 1 in 10 people)
?Dizziness.
?Headache.
?Respiratory infection.
?Low blood pressure. This may cause dizziness or fainting.
?Changes in blood test results:
- An increase in potassium levels in the blood, especially if you already have kidney problems or heart failure. If this is severe, you will feel tired, weak, have irregular heartbeats, or experience numbness.
?Effects on kidney function, especially if you already have kidney problems or heart failure. In rare cases, it may cause kidney failure.
Rare (may affect up to 1 in 10,000 people)
?Swelling of the face, lips, tongue, and/or throat.
?Decrease in red or white blood cells. You may feel tired, have an infection, or fever.
?Skin rash, hives.
?Itching.
?Back pain, joint and muscle pain.
?Changes in liver function, including inflammation of the liver (hepatitis). You will feel tired, have a yellowish discoloration of the skin and the white of the eyes, and symptoms similar to the flu.
?Nausea.
?Cough.
?Changes in blood test results:
Decrease in sodium levels in the blood. If severe, you may feel weak, lack energy, or have muscle cramps.
?Intestinal angioedema: swelling in the intestine, which presents with symptoms such as abdominal pain, nausea, vomiting, and diarrhea.
Frequency not known (cannot be estimated from available data):
?Diarrhea
Additional side effects in children and adolescents
In children treated for high blood pressure, side effects appear to be similar to those observed in adults, but occur more frequently. Throat pain is a very common side effect in children, but not described in adults. In turn, nasal discharge, fever, and increased heart rate are adverse side effects in children, but not described in adults.
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 the Pharmacovigilance of Medicines for Human Use:https://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 after the CAD initials. 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 trash. Dispose of packaging and medications you no longer need 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 Candesartán Ranbaxy
Each tablet contains 32 mg of candesartan cilexetil.
Appearance of the product and contents of the packaging
Candesartán Ranbaxy 32 mg are oval-shaped tablets, pink in color, marked with “C” and “12” in low relief on each side of the groove on one face and with a groove on the other face.
This medication is available:
In PVC/PE/PVdC-Alu blisters
Packaging sizes: 7, 8, 10, 12, 14, 15, 20, 28, 30, 40, 50, 56, 60, 70, 90, 95, 98, 100, 150 tablets.
Only some packaging sizes may be commercially marketed.
Marketing authorization holder and responsible manufacturer
Marketing authorization holder
Laboratorios Ranbaxy S.L.
Passeig de Gràcia, 9
08007 Barcelona
Spain
Responsible manufacturer
Sun Pharmaceutical Industries Europe B.V.
Polarisavenue 87
2132JH Hoofddorp
Netherlands
TERAPIA S.A.
124 Fabricii Street
400 632 Cluj Napoca,
Romania
This medication is authorized in the EEA member states with the following names:
Germany: CANDESARTAN BASICS 32 mg TablettenSpain: Candesartan Ranbaxy 32 mg tablets EFG
Italy: Candesartan Ranbaxy 32 mg compresse
Last review date of this leaflet: January 2025
Detailed and updated information about this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)www.aemps.gob.es
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