Candesartan Viatris 8 mg Tablets

2. What you need to know before you take Candesartan Viatris

Do not takeCandesartan Viatris

• If you are allergic to candesartan cilexetil or any of the other ingredients of this medicine (listed in section 6).
• If you have severe liver disease or biliary obstruction (problem with bile leaving the gallbladder).
• If you are more than 3 months pregnant. (In any case, it is better to avoid taking candesartan also at the start of your pregnancy – see section Pregnancy).
• If the patient is a child under 1 year of age.
• If you have diabetes or kidney problems and are being treated with a blood pressure-lowering medicine that contains aliskiren.

Warnings and precautions

Talk to your doctor before starting to take Candesartan Viatris:

• If you have heart, liver, or kidney problems or are undergoing dialysis.
• If you have recently had a kidney transplant.
• If you have vomited, have recently had severe vomiting, or have diarrhea.
• If you have a disease of the adrenal gland called Conn's syndrome (also known as primary hyperaldosteronism).
• If you have low blood pressure.
• If you have ever had a stroke.
• If you are taking any of the following medicines used to treat high blood pressure (hypertension):

• An Angiotensin-Converting Enzyme (ACE) inhibitor (such as enalapril, lisinopril, ramipril), especially if you have kidney problems related to diabetes.
• Aliskiren.
• If you are taking an ACE inhibitor, along with other specific medicines for the treatment of your heart failure, known as mineralocorticoid receptor antagonists (MRAs). These medicines are used to treat heart failure (see "Using Candesartan Viatris with other medicines").
• If you are pregnant, think you may be pregnant, or plan to become pregnant, you must inform your doctor. Candesartan is not recommended during the first trimester of pregnancy (first 3 months) and should not be taken after the third month of pregnancy as it may cause serious harm to your baby (see section Pregnancy).

Talk to your doctor if you experience abdominal pain, nausea, vomiting, or diarrhea after taking candesartan cilexetil. Your doctor will decide on the treatment to follow. Do not stop taking candesartan cilexetil on your own.

Your doctor may check your kidney function, blood pressure, and blood electrolyte levels (such as potassium) at regular intervals.

See also the information under the section "Do not take Candesartan Viatris".

If you are going to have surgery, inform your doctor or dentist that you are taking candesartan. This is because candesartan, in combination with some anesthetics, can cause a drop in blood pressure.

Children and adolescents

Candesartan has been studied in children. For more information, talk to your doctor. Candesartan should not be given to children under 1 year of age, due to the potential risk to kidney development.

Taking Candesartan Viatris with other medicines

Tell your doctor or pharmacist if you are taking or have recently taken or may take other medicines, including those obtained without a prescription.

Candesartan may affect how some medicines work and some medicines may affect the effect of candesartan. Your doctor may need to change your dose and/or take other precautions. If you are using certain medicines, your doctor may need to perform blood tests from time to time.

In particular, tell your doctor if you are using any of the following medicines:

• Other medicines to lower your blood pressure, including beta-blockers, diazoxide, and Angiotensin-Converting Enzyme (ACE) inhibitors (such as enalapril, captopril, lisinopril, or ramipril) or aliskiren (see also the information under the sections "Do not take Candesartan Viatris" and "Warnings and precautions").
• An ACE inhibitor along with other specific medicines for the treatment of your heart failure, known as mineralocorticoid receptor antagonists (MRAs) (such as spironolactone, eplerenone).
• Non-steroidal anti-inflammatory medicines (NSAIDs) such as ibuprofen, naproxen, diclofenac, celecoxib, or etoricoxib (medicines used to relieve pain and inflammation).
• Acetylsalicylic acid (if you take more than 3 g per day) (medicine to relieve pain and inflammation).
• Potassium supplements or salt substitutes that contain potassium (medicines that increase the amount of potassium in your blood).
• Heparin (a medicine to increase blood fluidity).
• Diuretics (medicines that promote urine elimination).
• Lithium (a medicine used to treat mental disorders).

Taking Candesartan Viatris with food and drink

• You can take candesartan with or without food.
• When prescribed candesartan, talk to your doctor before drinking alcohol. Alcohol may make you feel dizzy or faint.

Pregnancy and breastfeeding

Pregnancy

If you are pregnant, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before taking this medicine. Normally, your doctor will recommend that you stop taking candesartan before becoming pregnant or as soon as you know you are pregnant and will recommend another medicine. Candesartan is not recommended during the first trimester of pregnancy and should not be taken after the third month of pregnancy as it may cause serious harm to your baby.

Breastfeeding

If you are breastfeeding or plan to start breastfeeding, consult your doctor or pharmacist before taking this medicine. Candesartan is not recommended for women during this period, and your doctor may decide to administer a treatment that is more suitable if you want to breastfeed, especially newborns or premature babies.

Driving and using machines

Some patients may feel tired or dizzy when taking this medicine. If this happens to you, do not drive or use tools or machines.

Candesartan Viatris contains lactose

If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medicine.

3. How to take Candesartan Viatris

This is a long-term treatment.

Follow exactly the administration instructions of this medicine indicated by your doctor or pharmacist. In case of doubt, ask your doctor or pharmacist. It is important that you keep taking candesartan every day.

You can take Candesartan Viatris with or without food. Swallow the tablet with a little water. Try to take the tablet at the same time each day. This will help you remember to take it.

The tablet can be divided into equal doses.

Treatment of high blood pressure:

The recommended initial dose is 8 mg once a day. Your doctor may increase this dose up to 32 mg once a day depending on your 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 black patients may have a reduced response to this type of medicine when given as sole treatment, and these patients may need a higher dose.

Treatment of heart failure:

The recommended initial dose of candesartan is 4 mg once a day. Your doctor may increase this dose by doubling it at intervals of at least 2 weeks up to 32 mg once a day. Candesartan can be taken with other medicines for heart failure, and your doctor will decide what treatment is suitable for you.

Use in children and adolescents with high blood pressure:

Children from 6 to less than 18 years of age:

The recommended initial dose is 4 mg once a day.

For patients who weigh less than 50 kg, the doctor may decide to increase the dose up to a maximum of 8 mg once a day.

For patients who weigh 50 kg or more, the doctor may decide to increase the dose up to 8 mg once a day, and then up to 16 mg once a day if necessary.

If you take more Candesartan Viatris than you should

If you take more candesartan than your doctor told you, contact your doctor or pharmacist immediately or call the Toxicology Information Service (telephone 91 562 04 20) indicating the medicine and the amount taken. Your blood pressure may drop and you may feel tired.

If you forget to take Candesartan Viatris

Do not take a double dose to make up for forgotten doses. Simply take the next dose.

If you stop taking Candesartan Viatris

If you stop taking this medicine, your blood pressure may rise again. Therefore, do not stop taking candesartan without consulting your doctor.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

It is important that you know what these side effects may be.

Stop taking candesartan and talk to your doctor or go to the nearest emergency center if you have any of these symptoms:

Very rare(may affect up to 1 in 10,000 people)

• Swelling of the face, lips, tongue, and/or throat, which can cause difficulty breathing or swallowing.
• Increased number of infections that can cause fever, chills, sore throat, mouth ulcers, or bronchial cough. These symptoms could be indicative of a low white blood cell count (leucopenia).
• Changes in liver function, including liver inflammation (hepatitis), symptoms may be nausea, vomiting, loss of appetite, general feeling of discomfort, fever, itching, yellowing of the skin or the whites of the eyes, pale stools, or dark urine. These may be symptoms of serious liver problems.
• A decrease in kidney function, symptoms may be low urine production or absence of urine production, cloudy or bloody urine, pain when urinating, or lower back pain. These symptoms could be indicative of serious kidney problems. In very rare cases, kidney failure may occur.

Other possible side effects include:

Common(may affect up to 1 in 10 people)

• Dizziness/feeling of spinning when standing up (vertigo).
• Headache.
• Respiratory infection.
• Low blood pressure. This can cause dizziness or fainting.
• Increased potassium levels in the blood that can be seen in blood tests, especially if you already have kidney problems or heart failure. If this situation is severe, you may notice tiredness, weakness, an irregular heartbeat, or tingling in your hands or feet.

Very rare(may affect up to 1 in 10,000 people)

• Rash, hives.
• Itching.
• Cough.
• Back pain, joint and muscle pain.
• Feeling of discomfort (nausea).
• Changes in blood test results such as decreased sodium levels or increased liver enzymes in the blood.
• Intestinal inflammation with symptoms such as abdominal pain, nausea, vomiting, and diarrhea (intestinal angioedema).

Frequency not known(cannot be estimated from the available data)

• Diarrhea.

Other side effects in children and adolescents

In children treated for high blood pressure, side effects seem to be similar to those observed in adults, but occur more frequently. Sore throat is a very common side effect in children but has not been reported in adults, and runny nose, fever, and increased heart rate are common in children but have not been reported in adults.

Reporting of side effects

If you experience any side effects, talk to your doctor or pharmacist, even if it is possible that they are not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storage of Candesartan Viatris

Keep out of sight and reach of children.

Do not take this medicine after the expiry date which is stated on the carton, blister, or bottle after the abbreviation EXP. The expiry date is the last day of the month stated. After opening the bottle for the first time, use it within 100 days.

Do not store above 25°C. Store in the original package to protect from moisture.

Medicines should not be disposed of via wastewater or household waste. Place the cartons and medicines you no longer need in the SIGRE collection point at your usual pharmacy. Ask your pharmacist how to dispose of the cartons and medicines you no longer need. This will help protect the environment.

6. Container Contents and Additional Information

Composition of Candesartan Viatris

The active ingredient is candesartan cilexetil. Each tablet contains 8 mg of candesartan cilexetil.

The other ingredients are: calcium carmellose, hydroxypropylcellulose, lactose monohydrate (see section 2 "Candesartan Viatris contains lactose"), magnesium stearate, and mannitol.

Appearance of the Product and Container Contents

The tablets are white or almost white, round, biconvex, marked with the inscription "M" over "C5" on one side and smooth, with a break line on the other side.

Candesartan Viatris is available in blisters, with or without an envelope and inside a box, or an envelope of 7, 10, 14, 15, 28, 30, 50, 56, 60, 84, 90, 98, and 100 tablets, and in bottles of 30, 49, 56, 90, and 98 tablets. The envelopes and bottles contain a desiccant. The bottles may or may not contain cotton. The desiccant should not be ingested.

Only some pack sizes may be marketed.

Marketing Authorization Holder and Manufacturer

Marketing Authorization Holder

Viatris Limited

Damastown Industrial Park

Mulhuddart, Dublin 15

Dublin

Ireland

Manufacturer

McDermott Laboratories t/a Gerard Laboratories Ltd.

Unit 35/36 Baldoyle Industrial Estate

Grange Road, Dublin 13

Ireland

or

Mylan Hungary Kft.

Mylan utca 1

H-2900 Komárom

Hungary

or

Mylan Germany GmbH,

Zweigniederlassung Bad Homburg v. d. Hoehe, Benzstrasse 1

Bad Homburg v. d. Hoehe, Hessen, 61352

Germany

For further information about this medicinal product, please contact the local representative of the marketing authorization holder:

Viatris Pharmaceuticals, S.L.U.

C/ General Aranaz, 86

28027 - Madrid

Spain

This medicinal product is authorized in the Member States of the European Economic Area under the following names:

GermanyCandesartancilexetil Mylan 8 mg Tabletten

DenmarkKandrozid 8 mg tabletter

SpainCandesartán Viatris 8 mg comprimidos EFG

FinlandKandrozid 8 mg tabletit

NorwayKandrozid 8 mg tabletter

NetherlandsCandesartan cilexetil Viatris 8 mg tabletten

PortugalCandesartan Mylan 8 mg comprimidos

United KingdomCandesartan cilexetil 8 mg Tablets

SwedenKandrozid 8 mg tabletter

Date of the last revision of this leaflet:February 2025

Detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/