Medication info
Kobaratant Tablet 160/12.5 mg

Kobaratant Tablet 160/12.5 mg

Prescription medicationTablet경구
Ingredient · strength
Hydrochlorothiazide›12.5mg / 1 tabletValsartan›160mg / 1 tablet
Manufacturer / importer
하나제약(주)
Appearance
Dark red oval film-coated tablet
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 201007523 · Notified 2010.12.17 · Insurance code 657804530

Summary

Main use
Improvement of blood pressure control in essential hypertension
Who takes it
Adults
Adult dose
The recommended adult dosage is 1 tablet of Valsartan 80 mg / Hydrochlorothiazide 12.5 mg once daily, to be taken with a small amount of water regardless of meals. For Valsartan 160 mg / Hydrochlorothiazide 12.5 mg, this applies only if prescribed. For patients with renal impairment, mild to moderate renal impairment does not require dosage adjustment. For patients with hepatic impairment, mild to moderate hepatic impairment without cholestasis should not exceed a daily dose of 80 mg of Valsartan.

Ingredients

Manufacturer
하나제약(주)

Efficacy & effects

Improvement of blood pressure control in essential hypertension

  • Essential hypertension
View approved original text

This medication is used for patients with essential hypertension who have difficulty controlling blood pressure with monotherapy. It effectively lowers blood pressure and helps reduce the risk of cardiovascular diseases.

How to take

Adult dose

The recommended adult dosage is 1 tablet of Valsartan 80 mg / Hydrochlorothiazide 12.5 mg once daily, to be taken with a small amount of water regardless of meals. For Valsartan 160 mg / Hydrochlorothiazide 12.5 mg, this applies only if prescribed. For patients with renal impairment, mild to moderate renal impairment does not require dosage adjustment. For patients with hepatic impairment, mild to moderate hepatic impairment without cholestasis should not exceed a daily dose of 80 mg of Valsartan.

Precautions

This medication can cause serious harm to the fetus and newborn, especially during pregnancy, so it should be discontinued immediately if pregnancy is confirmed. People allergic to the components of this medication or sulfonamide drugs should not take it. It is contraindicated in patients with severely impaired liver or kidney function and certain liver diseases. Patients with electrolyte imbalances such as hypokalemia, hyponatremia, or hypercalcemia, as well as those suffering from certain endocrine disorders, should use it with caution. This medication may increase the risk of skin cancer, so sun exposure should be avoided, and skin condition should be regularly monitored. Dizziness or drowsiness may occur during treatment, so caution is needed when driving or operating machinery. Potassium supplements or potassium-containing medications should not be taken together without consulting a doctor, and blood potassium levels should be regularly monitored. Patients with renal or hepatic dysfunction should take the medication according to regular check-ups and medical advice. This medication may interact with other antihypertensives, diuretics, non-steroidal anti-inflammatory drugs (NSAIDs), so it's necessary to inform healthcare professionals about any drug use. In case of overdose, symptoms such as hypotension, arrhythmias, and electrolyte abnormalities may occur, requiring immediate medical treatment. Keep out of reach of children and store in a cool, dry place. Women who are pregnant or planning to become pregnant, and breastfeeding women should avoid taking this medication and consult healthcare professionals if necessary.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (including angioedema and edema), chest tightness, difficulty breathing, anaphylactic-like symptoms, angioedema, hepatitis, renal failure, hyperkalemia, hyponatremia, shock, loss of consciousness, agranulocytosis, leukopenia, thrombocytopenia, aplastic anemia, hemolytic anemia, necrotizing vasculitis, toxic epidermal necrolysis (Lyell syndrome), interstitial pneumonia, pulmonary edema, exacerbation of systemic lupus erythematosus, hypoglycemia, rhabdomyolysis

Mild side effects

  • Headache
  • dizziness
  • rhinitis
  • fatigue
  • low back pain
  • cough
  • upper respiratory infection
  • diarrhea
  • joint pain
  • abdominal pain
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  • epigastric pain
  • blurred vision
  • visual disturbances
  • anxiety
  • arthritis
  • bronchitis
  • acute bronchitis
  • chest pain
  • orthostatic dizziness
  • dry mouth
  • dyspepsia
  • difficulty breathing
  • erectile dysfunction
  • colitis
  • sweating
  • sensory impairment
  • insomnia
  • hypokalemia
  • hypotension
  • influenza
  • muscle cramps
  • myalgia
  • nausea
  • nasal congestion
  • nasal bleeding
  • throat pain

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

Storage

This medication is sensitive to air and moisture, so it should be stored in a tightly closed container. Also, it should be kept in a cool place below 30 degrees Celsius to maintain its effectiveness.

Appearance and packaging

Appearance

Dark red oval film-coated tablet

Package unit

30 tablets/bottle, 100 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.