Cantavel A Tablets 16/10/40 Milligrams

Adult dose

Take 1 tablet once daily with or without food. It is recommended to take it at the same time each day (e.g., in the morning). The dosage should be individualized based on the effectiveness and tolerance of Candesartan Cilexetil/Amlodipine combination and Atorvastatin. For patients whose blood pressure is not controlled, the following doses of Candesartan Cilexetil/Amlodipine combination are recommended: - 8/5

This medication can cause serious harm to the fetus and newborn if taken during pregnancy; therefore, it should be discontinued immediately upon confirmation of pregnancy. If any issues arise with muscles or if there is a significant increase in muscle-related lab results, this medication should be discontinued, and caution is advised if there is a risk of severe muscle damage. This medication should not be used in individuals with allergies to specific components, pregnant or nursing women, severe liver disease, severe kidney disease, or individuals with hereditary angioedema. Elderly patients, those with hyperkalemia, liver impairment, hypotension, heart valve disease, kidney impairment, etc., should be carefully monitored while using this medication. During the course of this treatment, side effects such as dizziness, headache, edema, muscle pain, dyspepsia, liver function abnormalities, skin rash, and hypotensive symptoms may occur, and if any symptoms arise, consultation with a physician is recommended. This medication lowers blood pressure, so patients may experience symptoms of hypotension or changes in kidney function. Regular monitoring of blood pressure and blood tests is necessary. This medication can interact with others; notify your healthcare provider or pharmacist of any additional medications being taken. Dizziness or drowsiness may occur when driving or operating machinery, so caution is advised. If symptoms such as muscle pain, weakness, fever, or malaise occur during treatment, notify the healthcare provider immediately, and if liver function abnormalities are detected, therapy should be discontinued and medical attention sought. Dosage adjustments may be necessary for patients with certain liver diseases or decreased kidney function, and routine clinical monitoring is advised.

Serious side effects

Hives, severe swelling (edema), difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, peeling skin, pain in the mouth/eyes, yellowing of the skin or eyes (jaundice), extreme lethargy, sudden and severe headache, thunderclap headache, seizures, confusion, visual abnormalities, paralysis, significantly reduced urine output, significant swelling of the body accompanied by high blood pressure, severe allergic reactions,

Mild side effects

• Dizziness
• headache
• fainting
• chest pain
• swelling
• palpitations
• urinary tract infection
• increased blood pressure
• gastrointestinal pain
• orthostatic hypotension

This medication should be stored in a tightly sealed container to protect it from air and moisture, at a temperature between 1 and 30 degrees Celsius. Proper storage will help maintain the medication's effectiveness and prevent degradation.

Appearance

Blue rectangular film-coated tablet

Package unit

30 tablets/PTP, 10 tablets/PTP