Nuborjet Tablet 80/2.5/10/10 Milligrams

Adult dose

This medication is administered only to adults, with a prescribed dosage of one tablet once daily, regardless of meals, along with water. It is recommended to take it at the same time every day. The recommended dosage for the telmisartan/S-amlodipine (amlodipine) combination is once daily. The dosage for each ingredient should be adjusted, and if blood pressure control is inadequate, a switch to the combination product may be considered. The dosage range for the rosuvastatin/ezetimibe combination is once daily.

This medication can cause serious harm to the fetus if taken during pregnancy, especially in the second and third trimesters. If pregnant, use should be discontinued immediately. If symptoms like muscle pain or weakness occur, consult a doctor immediately as severe cases may lead to renal dysfunction. Patients with liver function problems or a history of liver disease should consult a doctor before taking this medication and should undergo regular liver function tests. Patients with severe renal impairment, certain liver diseases, or muscle disorders should not use this medication. Patients with excessively low blood pressure or severe heart failure, acute myocardial infarction, or other cardiovascular issues need to take caution with this medication. This medication may increase blood potassium levels, so patients at risk of hyperkalemia should frequently check potassium levels through blood tests. When taken with other antihypertensives or lipid-lowering agents, there is a possibility of drug interactions, so it should be taken according to a doctor's guidance. Caution is needed when driving or operating machinery as dizziness or drowsiness may occur. If allergic reactions such as skin rash, difficulty breathing, or swelling of the face or lips occur while taking this medication, it should be discontinued immediately and medical personnel informed. This medication contains lactose, so patients with lactose intolerance should avoid it. Regular monitoring of blood pressure, liver function, renal function, blood lipids, and muscle condition is necessary while taking this medication.

Serious side effects

Hives, angioedema, laryngeal edema, difficulty breathing, anaphylactic reactions, severe skin adverse reactions (Stevens-Johnson syndrome, toxic epidermal necrolysis, erythema multiforme, drug-induced liver damage), severe muscle disorders (rhabdomyolysis, myositis, myopathy), liver dysfunction (hepatitis, acute hepatitis, toxic hepatitis, jaundice), interstitial lung disease, severe edema, thrombocytopenia, syncope, shock, hypotension, loss of consciousness, renal failure, acute

Mild side effects

• Increased ALT
• increased AST
• increased Ɣ-GTP
• edema
• orthostatic hypotension
• hyperkalemia
• headache
• dizziness
• cough
• abdominal pain

This medication should be stored in a tightly sealed container to prevent exposure to air or moisture, and it is safe to store at room temperature between 1 degree and 30 degrees Celsius. Proper storage helps maintain the medication's efficacy and prevent degradation.

Appearance

Yellow oval film-coated tablet

Package unit

30 tablets/bottle