Medication info
Cansata Tablet 16 mg (Candesaartan Cilexetil)

Cansata Tablet 16 mg (Candesaartan Cilexetil)

Prescription medicationTablet경구
Ingredient · strength
Candesartan Cilexetil›16mg / 1 tablet
Manufacturer / importer
경동제약(주)
Appearance
Light pink tablet, convex on both sides with a line for splitting on one side
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 201007652 · Notified 2010.12.22 · Insurance code 648102970

Summary

Main use
Treatment of essential hypertension and heart failure (left ventricular dysfunction)
Who takes it
Adults · Children
Adult dose
In the case of essential hypertension, the initial and maintenance dose is 8 to 16 mg of Candesaartan Cilexetil orally once daily. If blood pressure is not controlled after 4 weeks of treatment at 16 mg once daily, the dose may be increased to a maximum of 32 mg once daily. For heart failure, the initial dose is 4 mg once daily, and the dose may be doubled at intervals of at least 2 weeks to a maximum of 32 mg once daily.
Child dose
Safety and efficacy in patients under 18 years of age have not been established.

Ingredients

Manufacturer
경동제약(주)

Efficacy & effects

Treatment of essential hypertension and heart failure (left ventricular dysfunction)

  • Essential hypertension
  • heart failure
  • impaired left ventricular contractile function
  • reduced left ventricular ejection fraction
View approved original text

This medication is used to treat essential hypertension, which is high blood pressure of unknown cause. It is especially helpful for heart failure patients with impaired left ventricular contractile function that leads to decreased heart function. It is also effective for heart failure patients who need to take additional ACE inhibitors or who do not tolerate ACE inhibitors well. This helps control blood pressure and alleviate the heart's burden, thus improving symptoms. Therefore, it is widely used in the treatment of essential hypertension and heart failure.

How to take

Adult dose

In the case of essential hypertension, the initial and maintenance dose is 8 to 16 mg of Candesaartan Cilexetil orally once daily. If blood pressure is not controlled after 4 weeks of treatment at 16 mg once daily, the dose may be increased to a maximum of 32 mg once daily. For heart failure, the initial dose is 4 mg once daily, and the dose may be doubled at intervals of at least 2 weeks to a maximum of 32 mg once daily.

Child dose

Safety and efficacy in patients under 18 years of age have not been established.

Precautions

This medication can cause serious harm to the fetus during pregnancy, so it must be stopped immediately upon confirmation of pregnancy. Patients who are allergic to this drug or its ingredients, pregnant or nursing women, those with severe liver disease or cholestasis, patients with a history of angioedema, and those with certain genetic disorders should not take this medication. Elderly patients, those with weakened kidney function, patients with hyperkalemia, and those with heart valve diseases should take this medication with caution, and blood pressure, kidney function, and serum potassium levels should be monitored regularly during treatment. Side effects such as dizziness, back pain, respiratory infections may occur; in severe cases, hypotension, worsening kidney function, and blood abnormalities may arise. If unusual symptoms occur, a doctor should be consulted immediately. There may be interactions with other medications, so it is essential to inform the doctor or pharmacist, particularly when taken in combination with potassium-sparing diuretics or non-steroidal anti-inflammatory drugs. Women who are pregnant or planning to become pregnant should not use this medication, and nursing mothers should also avoid taking it. If unavoidable, breastfeeding should be discontinued. In case of overdose, symptoms such as hypotension, dizziness, and rapid heartbeat may occur, so appropriate treatment must be sought at a medical institution immediately. This medication should be stored out of reach of children and should not be transferred to another container for safety. Caution is needed while driving or operating machinery as dizziness may occur.

Side effects and when to seek care immediately

Serious side effects

Urticaria, angioedema (swelling of the face, lips, tongue, pharynx, or larynx), cold sweat, kidney dysfunction, jaundice, liver dysfunction, shock, syncope, loss of consciousness, paralysis, rash (severe skin reactions)

Mild side effects

  • Dizziness
  • back pain
  • respiratory infections
  • fatigue
  • peripheral edema
  • chest pain
  • headache
  • bronchitis
  • cough
  • sinusitis
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  • nausea
  • abdominal pain
  • diarrhea
  • vomiting
  • joint pain
  • proteinuria
  • weakness
  • fever
  • abnormal sensations
  • indigestion
  • gastroenteritis
  • tachycardia
  • palpitations
  • elevated creatine kinase
  • hyperglycemia
  • hypertriglyceridemia
  • hyperuricemia
  • myalgia
  • epistaxis
  • anxiety
  • depression
  • drowsiness
  • rash
  • increased sweating
  • hematuria
  • leukopenia
  • neutropenia

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a tightly closed container to prevent exposure to air or moisture. It is advisable to maintain a storage temperature between 1 to 30 degrees Celsius.

Appearance and packaging

Appearance

Light pink tablet, convex on both sides with a line for splitting on one side

Package unit

30 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.