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Candesartan (Pro Doc): Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx)
Strength:
8 mg, 16 mg, 32 mg
Active ingredient:

Patient Medication Information: uses, side effects, how to take - Candesartan (Pro Doc)

ABOUT THIS MEDICATION

What the medication is used for:

Candesartan is used to treat:

  • High Blood Pressure in Adults
  • High Blood Pressure in Children (6 to 17 years of age)

  • Heart Failure in Adults

What it does:

Candesartan is an angiotensin receptor blocker (ARB). You can recognize an ARB because its medicinal ingredient ends in“-SARTAN”.

This medicine does not cure your disease. It helps to control it. Therefore, it is important to continue taking Candesartan regularly even if you feel fine.

Its main action is to relax the arteries, letting the blood flow more freely, thereby lowering the blood pressure.

When it should not be used:

Do not take Candesartan if you:

  • Are allergic to candesartan cilexetil or to any non-

    medicinal ingredient in the formulation.

  • Have experienced an allergic reaction (angioedema) with

    swelling of the hands, feet, or ankles, face, lips, tongue, throat, or sudden difficulty breathing or swallowing, to any ARB. Be sure to tell your doctor, nurse, or pharmacist that this has happened to you.

  • Are already taking a blood pressure-lowering medicine

    that contains aliskiren (such as Rasilez®) and you have diabetes or kidney disease.

  • Are pregnant or intend to become pregnant. Taking

    Candesartan during pregnancy can cause injury and even death to your baby.

  • Are breastfeeding. It is possible that Candesartan passes

    into breast milk.

  • Are less than 1 year old
  • Have one of the following rare hereditary diseases:

    • Galactose intolerance
    • Lapp lactase deficiency
    • Glucose-galactose malabsorption

Because lactose monohydrate is a non-medicinal ingredient in Candesartan.

What the medicinal ingredient is:

Candesartan cilexetil.

What the nonmedicinal ingredients are:

Carrageenan, cornstarch, croscarmellose sodium, lactose monohydrate, magnesium stearate and povidone.The 8 mg, 16 mg and 32 mg tablets also contain ferric oxide red and titanium dioxide.

What dosage forms it comes in:

Tablets: 8 mg, 16 mg and 32 mg.

WARNINGS AND PRECAUTIONS

Serious Warnings and Precautions - Pregnancy Candesartan should not be used during pregnancy. If you discover that you are pregnant while taking Candesartan, stop the medication and contact your doctor, nurse or pharmacist as soon as possible.

BEFORE you use Candesartan talk to your doctor, nurse or pharmacist if you:

  • Have experienced an allergic reaction to any drug used to lower blood pressure, including angiotensin converting enzyme (ACE) inhibitors.
  • Have narrowing of an artery or a heart valve.
  • Have had a heart attack or stroke.
  • Have heart failure.
  • Have diabetes, heart, liver or kidney disease.
  • Are on dialysis.
  • Are dehydrated or suffer from excessive vomiting, diarrhea, or sweating.
  • Are taking a salt substitute that contains potassium, potassium supplements, or a potassium-sparing diuretic (a specific kind of “water pill” that makes your body keep potassium) or other drugs that may increase potassium levels (e.g., heparin, co-trimoxazole)..
  • Are on a low-salt diet.
  • Are taking a medicine that contains aliskiren, such as

    Rasilez®, used to lower high blood pressure. The combination with Candesartan is not recommended.

  • Are taking an angiotensin converting enzyme (ACE)

    inhibitor. You can recognize ACE inhibitors because their medicinal ingredient ends in “-PRIL”.

  • Are taking an ACE-inhibitor together with a medicine which belongs to the class of medicines known as mineralocorticoid receptor antagonists (for example, spironolactone, eplerenone). These medicines are for the treatment of heart failure.

Driving and using machines: Before you perform tasks which may require special attention, wait until you know how you respond to Candesartan. Dizziness, lightheadedness, or fainting can especially occur after the first dose and when the dose is increased.

If you are currently taking Candesartan and are going to have an operation, be sure to tell your doctor or dentist about your medication before you are given an anaesthetic.

INTERACTIONS WITH THIS MEDICATION

As with most medicines, interactions with other drugs are possible. Tell your doctor, nurse, or pharmacist about all the medicines you take, including drugs prescribed by other doctors, vitamins, minerals, natural supplements, or alternative medicines.

The following may interact with Candesartan:

  • Agents increasing serum potassium, such as a salt

    substitute that contains potassium, potassium supplements, a potassium-sparing diuretic (a specific kind of “water pill”) or other drugs that may increase potassium levels (e.g., heparin, co-trimoxazole)..

  • Lithium used to treat bipolar disease.
  • Nonsteroidal anti-inflammatory drugs (NSAIDs), used to

    reduce pain and swelling. Examples include ibuprofen, naproxen, and celecoxib.

  • Blood pressure- lowering drugs, including diuretics

    (“water pills”), aliskiren-containing products (e.g. Rasilez®) or angiotensin converting enzyme (ACE) inhibitors.

  • Mineralocorticoid receptor antagonists (for example,

    spironolactone, eplerenone) and ACE inhibitors used in heart failure.

PROPER USE OF THIS MEDICATION

The dosage of Candesartan is individualized.

Take Candesartan exactly as prescribed. It is recommended to take your dose at about the same time everyday.

Candesartan is taken once a day. Even if your doctor has prescribed 2 tablets a day, both should be taken at the same time, unless otherwise indicated.

Candesartan may be taken with food or on an empty stomach but it should be taken consistently the same way each day.

Swallow Candesartan with a glass of water.

Usual Dose:

Lower doses may be required based on the other medications you take and the presence of other disease conditions.

High Blood Pressure in Adults:

Recommended Initial Dose: 16 mg once a day.

Total Daily Dose: 8 mg to 32 mg once a day.

High Blood Pressure in Children (6 to 17 years of age):

  • For children who weigh less than 50 kg:

    Recommended Starting Dose: 4 mg once a day. Maximum Dose: 8 mg once a day

    • For children who weigh 50 kg or more:

      Recommended Starting Dose: 8 mg once a day. Maximum Dose: 16 mg once a day

Candesartan must not be given to children under 1 year of age due to the potential risk to the developing kidneys.

Heart Failure in Adults:

Usual Recommended Initial Dose: 4 mg once a day. If tolerated by the patient, this dose is gradually doubled (approximately every 2 weeks) until the target dose is reached. Target Dose: 32 mg once a day.

Overdose:

If you think you, or a person you are caring for, have taken too much Candesartan, contact a healthcare professional, hospital emergency department or regional poison control centre immediately, even if there are no symptoms.

Missed Dose:

If you miss a dose of Candesartan and remember within 12 hours, you should take your usual dose as soon as possible. Then go back to your regular schedule. But if it is more than 12 hours when you remember, do not take the missed dose. Just take the next dose on time.

Never take a double dose of Candesartan to make up for missed tablets. If you are still unsure, check with your doctor or pharmacist to see what you should do.

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

Side effects may include:

  • dizziness, falls
  • drowsiness, insomnia
  • rash
  • diarrhea, vomiting
  • headache
  • back or leg pain, muscle cramps
  • cough
  • sore throat
  • dry mouth
  • cold symptoms
  • pneumonia
  • fainting spells
  • confusion

Side effects in adults and children are similar, but may occur more often in children.

If any of these affects you severely, tell your doctor, nurse or pharmacist.

Candesartan can cause abnormal blood test results. Your doctor will decide when to perform blood tests and will interpret the results.

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM

Symptom / effectTalk with your healthcare professionalStop taking drug and get immediate medical help
Only if severeIn all cases

Low Blood

Pressure:

dizziness, fainting, lightheadedness

√
Fast, Slow or Irregular Heart Beat√

Increased levels of potassium in the blood:

Irregular heartbeats, muscle weakness and generally

feeling unwell

√

Allergic Reaction:

rash, hives, swelling of the face, lips, tongue or throat, difficulty

swallowing or

breathing

√

Kidney Disorder:

change in

frequency of

urination, nausea, vomiting, swelling of extremities, fatigue.

√
Hematuria (blood in urine)√

Liver Disorder:

yellowing of the skin or eyes, dark urine, abdominal pain, nausea,

vomiting, loss of appetite

√

Shortness of

breath, difficulty breathing

(Dyspnea,

Pulmonary edema)

√

Rhabdomyolysis:

muscle pain that you cannot

explain, muscle tenderness or

weakness, dark brown urine

√

Decreased

Platelets: bruising, bleeding, fatigue and weakness

√
Symptom / effectTalk with your healthcare professionalStop taking drug and get immediate medical help
Only if severeIn all cases

Inflammation of the Pancreas:

abdominal pain that lasts and gets worse when you lie down, nausea and vomiting

√
Chest Pain√

Stroke

(cerebrovascular accident): face or arm weakness, abnormal speech and blurred vision, loss of

consciousness

√

This is not a complete list of side effects. For any unexpected effects while taking Candesartan, contact your doctor, nurse or pharmacist.

HOW TO STORE IT

  • When you first open the package, if you find any damage to the plastic seal or foil which exposes the tablet, ask your pharmacist to check the package.
  • Candesartan tablets are protected in their package, it is best to keep the tablets in their original package at normal room temperature and in a dry place. Do not keep Candesartan in the bathroom.
  • Keep out of sight and reach of children. Never take medicine in front of small children as they will want to copy you.
  • Do not keep or use Candesartan after the expiry date indicated on the package. Unused medicines which you know you will no longer need should be carefully discarded. You may wish to seek advice from your pharmacist.
  • Remember to get a new prescription from your doctor or a refill from your pharmacy a few days before all your tablets are taken.

Reporting Side Effects

You can report any suspected side effects associated with the use of health products to Health Canada by:

  • Visiting the Web page on Adverse Reaction Reporting

    (https://www.canada.ca/en/health-

    canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting.html) for information on how to report online, by mail or by fax; or

  • Calling toll-free at 1-866-234-2345.

NOTE: Contact your health professional if you need information about how to manage your side effects. The Canada Vigilance Program does not provide medical advice.

MORE INFORMATION

If you want more information about Candesartan:

  • Talk to your healthcare professional.
  • Find the full Product Monograph that is prepared for healthcare professionals and includes this Consumer Information by visiting the Health Canada website (https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/drug-product-database.html); or by contacting Pro Doc Ltée at 1-800-361-8559, www.prodoc.qc.ca or

    info@prodoc.qc.ca.

Pro Doc Ltée Laval, Quebec H7L 3W9.

Last revised: November 10, 2021

Rasilez® is a registered trademark of Novartis AG.

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02377934

Revision date stated in the text: November 10, 2021

Found a mistake? Write to us via the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Candesartan (Pro Doc)

Rx or OTC
Prescription (Rx)?
DIN 02377934, 02377942, 02422069
Schedule(s) PRESCRIPTION
Active ingredient(s) Candesartan cilexetil
Dosage form(s) Tablet
Route(s) of administration Oral
Drug class (WHO ATC)
  1. C Cardiovascular system drugs
    1. C09 Agents acting on the renin-angiotensin system
      1. C09C Angiotensin II receptor blockers (ARBs), plain
        1. C09CA Angiotensin II receptor blockers (ARBs), plain
          1. C09CA06 Candesartan
Company PRO DOC LIMITEE
Current status Marketed
Strengths and forms
DIN Strength Dosage form(s) Current status
02377934 8 MG Tablet Marketed February 8, 2012
02377942 16 MG Tablet Marketed February 8, 2012
02422069 32 MG Tablet Marketed June 5, 2014

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.