Medication info

Baotan Plus Tablets 80/12.5 mg

Prescription medicationTablet경구Expired
Ingredient · strength
Valsartan›80mg / 1 tabletHydrochlorothiazide›12.5mg / 1 tablet
Manufacturer / importer
한국넬슨제약(주)
Appearance
Pink oval film-coated tablets
Packaging
30 tablets, 100 tablets
Approval status
Expired

MFDS item code 201508453 · Approved 2015.12.28

This product's status changed to Expired on 2025.12.28. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improves blood pressure control in essential hypertension
Who takes it
Adults
Adult dose
The recommended dosage for adults is one tablet of Valsartan 80 mg/Hydrochlorothiazide 12.5 mg once daily, taken with a small amount of water, regardless of meals. Valsartan 160 mg/Hydrochlorothiazide 12.5 mg applies if prescribed for blood pressure reduction. Patients with kidney impairment do not require dosage adjustments for mild to moderate kidney impairment (creatinine clearance of 30 mL/min or more). Patients with liver impairment should not exceed 80 mg of Valsartan daily.

Ingredients

Manufacturer
한국넬슨제약(주)

Efficacy & effects

Improves blood pressure control in essential hypertension

  • Essential hypertension
View approved original text

This medication is used in patients with essential hypertension whose blood pressure is not adequately controlled by monotherapy. It is administered additionally to improve blood pressure when existing treatments alone are insufficient.

How to take

Adult dose

The recommended dosage for adults is one tablet of Valsartan 80 mg/Hydrochlorothiazide 12.5 mg once daily, taken with a small amount of water, regardless of meals. Valsartan 160 mg/Hydrochlorothiazide 12.5 mg applies if prescribed for blood pressure reduction. Patients with kidney impairment do not require dosage adjustments for mild to moderate kidney impairment (creatinine clearance of 30 mL/min or more). Patients with liver impairment should not exceed 80 mg of Valsartan daily.

Precautions

This medication can cause serious harm to the fetus if taken during pregnancy, especially in the second and third trimesters, so it should be discontinued immediately if pregnancy is confirmed. Patients with allergies to this medication or its components, or those with specific liver or kidney diseases, should not take this medication. Electrolyte imbalance or changes in renal function should be carefully monitored during treatment, and caution should be exercised in elderly patients or those with heart disease. This medication may cause dizziness or drowsiness, hence caution is advised when driving or operating machinery. Potassium supplements or potassium-containing medications should not be taken without consulting a physician, and caution is particularly necessary in cases of dehydration, excessive sweating, diarrhea, or vomiting as blood pressure may drop sharply. This medication can interact with other antihypertensives, lithium, non-steroidal anti-inflammatory drugs (NSAIDs), so it is essential to inform your doctor or pharmacist about any other medications you are taking. The skin may become more sensitive to sunlight, so sun exposure should be avoided, and any skin abnormalities should be discussed with a healthcare provider. Severe side effects may include angioedema, hepatitis, renal failure, and electrolyte disorders, and you should discontinue use and consult a healthcare facility immediately if any abnormal symptoms occur. It is advisable to avoid using this medication in children, pregnant women, and nursing mothers as its safety has not been established. This medication should be stored away from moisture and direct sunlight and kept out of reach of children.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (angioedema), chest tightness, difficulty breathing, anaphylaxis-like symptoms, angioedema (swelling of the face, lips, throat, tongue), hepatitis, renal failure, hyperkalemia, hyponatremia (accompanied by malaise, loss of appetite, nausea, vomiting, altered consciousness), shock, fainting, loss of consciousness, agranulocytosis, leukopenia, thrombocytopenia, aplastic anemia, hemolytic anemia, necrotizing vasculitis, toxic epidermal necrolysis (Lyell's syndrome

Mild side effects

  • Headache
  • dizziness
  • nasopharyngitis
  • fatigue
  • lower back pain
  • cough
  • upper respiratory infection
  • diarrhea
  • arthralgia
  • abdominal pain
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  • epigastric pain
  • blurred vision
  • visual disturbances
  • anxiety
  • arthritis
  • bronchitis
  • acute bronchitis
  • chest pain
  • orthostatic dizziness
  • dry mouth
  • dyspepsia
  • erectile dysfunction
  • enteritis
  • sweating
  • sensory impairment
  • insomnia
  • hypokalemia
  • hypotension
  • influenza
  • muscle cramps
  • myositis
  • nausea
  • nasal congestion
  • nasal bleeding
  • throat pain
  • otitis media

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 sealed container. Additionally, it should be kept in a cool place below 30 degrees Celsius to maintain its efficacy.

Appearance and packaging

Appearance

Pink oval film-coated tablets

Package unit

30 tablets, 100 tablets

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.