Medication info
TruStar Tablet 80/5 mg

TruStar Tablet 80/5 mg

Prescription medicationTablet경구
Ingredient · strength
Telmisartan›80mg / 1 tabletRosuvastatin Calcium›5.2mg / 1 tablet
Manufacturer / importer
진양제약(주)
Appearance
Light pink oval film-coated tablet
Packaging
30 tablets (10 tablets x 3 PTP)
Approval status
Active

MFDS item code 201505199 · Approved 2015.07.31 · Insurance code 650303420

Summary

Main use
Treatment of hypertension and hyperlipidemia (reduction of cardiovascular disease risk)
Who takes it
Adults
Adult dose
Telmisartan: For essential hypertension, it is recommended to administer 40 mg orally once daily, which may be effective at 20 mg once daily for some patients. If needed, the dose may be increased up to 80 mg once daily. For reduction of cardiovascular disease risk, it is recommended to administer 80 mg orally once daily. For patients with liver impairment, do not exceed 40 mg once daily. Rosuvastatin Calcium: Primary hypercholesterolemia (including heterozygous familial hypercholesterolemia, type IIa), combined hyperlipidemia (type IIb), primary dysbetalipoproteinemia (type III), and homozygous familial hypercholesterolemia. Patients should follow a standard cholesterol-lowering diet before and during treatment, which should be maintained throughout the treatment period. This medication can be taken at any time of the day, regardless of meals. The initial dose is 5 mg once daily, and doses may be adjusted to achieve a greater reduction in LDL-C levels based on individual requirement. The maintenance dose is usually set at 10 mg once daily, and most patients are maintained at this dose. The maintenance dose should be adjusted appropriately based on LDL-C levels, treatment targets, and patient response, with a maximum increase of 20 mg daily.

Ingredients

Manufacturer
진양제약(주)

Efficacy & effects

Treatment of hypertension and hyperlipidemia (reduction of cardiovascular disease risk)

  • Essential hypertension
  • hypercholesterolemia
  • heterozygous familial hypercholesterolemia
  • combined hyperlipidemia
  • homozygous familial hypercholesterolemia
  • dysbetalipoproteinemia
  • elevated high-sensitivity C-reactive protein
  • hypertension
  • low HDL-cholesterol levels
  • smoking
  • early family history of coronary artery disease
View approved original text

This medication is used for patients who need to take two medications, telmisartan and rosuvastatin, simultaneously. Telmisartan is primarily administered to patients with essential hypertension or those at high risk of cardiovascular diseases such as myocardial infarction or stroke. It is particularly effective in high-risk diabetic patients who cannot use ACE inhibitors. Meanwhile, rosuvastatin helps manage hypercholesterolemia and combined hyperlipidemia and is used as an adjunct when diet alone does not control the condition. Furthermore, it contributes to reducing the risk of cardiovascular diseases, including stroke and myocardial infarction, and reduces risks after vascular revascularization. By administering both medications together, it effectively manages cardiovascular health by improving hypertension and dyslipidemia simultaneously.

How to take

Adult dose

Telmisartan: For essential hypertension, it is recommended to administer 40 mg orally once daily, which may be effective at 20 mg once daily for some patients. If needed, the dose may be increased up to 80 mg once daily. For reduction of cardiovascular disease risk, it is recommended to administer 80 mg orally once daily. For patients with liver impairment, do not exceed 40 mg once daily. Rosuvastatin Calcium: Primary hypercholesterolemia (including heterozygous familial hypercholesterolemia, type IIa), combined hyperlipidemia (type IIb), primary dysbetalipoproteinemia (type III), and homozygous familial hypercholesterolemia. Patients should follow a standard cholesterol-lowering diet before and during treatment, which should be maintained throughout the treatment period. This medication can be taken at any time of the day, regardless of meals. The initial dose is 5 mg once daily, and doses may be adjusted to achieve a greater reduction in LDL-C levels based on individual requirement. The maintenance dose is usually set at 10 mg once daily, and most patients are maintained at this dose. The maintenance dose should be adjusted appropriately based on LDL-C levels, treatment targets, and patient response, with a maximum increase of 20 mg daily.

Precautions

This medication can cause severe harm to the fetus and newborn during pregnancy; thus, it should be discontinued immediately upon confirmation of pregnancy. Patients who are allergic to this medication, pregnant, or breastfeeding women, and fertile women who do not use adequate contraceptive methods should not take it. Patients with severely impaired liver function or those with biliary excretion issues, and patients with muscle diseases should use caution when administering this medication. Patients with very poor renal function or those taking certain immunosuppressants, as well as diabetic patients with decreased renal function, should ideally not use this medication. Since this medication contains lactose, patients with lactose intolerance or specific genetic metabolic disorders should not take it. Elderly patients, patients with elevated serum potassium levels, and patients with slightly impaired liver function should use this medication carefully, and liver and muscle function tests should be performed regularly. If muscle-related symptoms such as myalgia, muscle weakness, or muscle cramps occur, consult a physician immediately, and discontinue use if necessary. This medication may interact with other antihypertensive agents or lipid-lowering agents, so you should inform your physician about any other medications you are taking. During treatment with this medication, abnormalities in liver function, blood pressure decreases, allergic reactions, or angioedema may occur, so symptoms should be reported to healthcare professionals immediately. Be cautious as dizziness or drowsiness may occur while driving or operating dangerous machinery.

Side effects and when to seek care immediately

Serious side effects

Hives, angioedema (severe swelling), chest tightness, difficulty breathing, cold sweat, pallor, severe rash accompanied by high fever, blisters, skin peeling, pain in oral/ocular mucosa, difficulty breathing, asthma attacks, respiratory abnormalities accompanied by coughing and fever, yellowing of the skin or eyes (jaundice), general malaise, sudden and severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis, markedly reduced urine output

Mild side effects

Headache, orthostatic dizziness, sleep paralysis, blood pressure increase or decrease, hypotension, urinary tract pain, rhinitis, discomfort in the oropharynx, pulmonary disease, gastrointestinal abnormalities (abdominal pain, diarrhea, dyspepsia, vomiting, abdominal discomfort, abdominal bloating), myalgia, muscle cramps, arthralgia, limb pain, tinnitus, hearing loss, bad breath, fatty liver, sensory loss, movement disorder, frequent urination, depression, insomnia, anxiety, increased serum creatinine, increased serum uric acid

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

Storage

This medication should be stored in a tightly sealed container to avoid exposure to air or moisture. It is recommended to maintain storage temperature between 1 degree and 30 degrees Celsius.

Appearance and packaging

Appearance

Light pink oval film-coated tablet

Package unit

30 tablets (10 tablets x 3 PTP)

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.

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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.