Medication info
New Bicaplus Tablet 10/40/12.5 mg

New Bicaplus Tablet 10/40/12.5 mg

Prescription medicationTablet경구
Ingredient · strength
Olmesartan Medoxomil›40mg / 1 tabletAmlodipine Besylate›13.888mg / 1 tabletHydrochlorothiazide›12.5mg / 1 tablet
Manufacturer / importer
대한뉴팜(주)
Appearance
Gray-red, round film-coated tablet
Packaging
30 tablets/PTP [10 tablets/Alu-Alu×3]
Approval status
Active

MFDS item code 201805263 · Approved 2018.12.26 · Insurance code 669907330

Summary

Main use
Improvement of blood pressure control in essential hypertension
Who takes it
Adults · Children
Adult dose
This medication is taken once daily at 1 tablet, with or without food. It is recommended to take it at the same time every day (e.g., in the morning) if possible. The recommended dosage is as follows: - 5/20/12.5 mg: Administered to patients whose blood pressure is not adequately controlled with the combination therapy of Amlodipine/Olmesartan Medoxomil 5/20 mg. - 5/40/12.5 mg: Administered to patients whose blood pressure is not adequately controlled with the combination therapy of Amlodipine/Olmesartan Medoxomil 5/40 mg.
Child dose
The safety and efficacy of this medication have not been established in patients under 18 years of age, and its use is not recommended.

Ingredients

Manufacturer
대한뉴팜(주)

Efficacy & effects

Improvement of blood pressure control in essential hypertension

  • Essential hypertension
View approved original text

This medication is used to effectively lower blood pressure and reduce the risk of cardiovascular complications in patients with essential hypertension whose blood pressure is not sufficiently controlled with a combination therapy of Amlodipine and Olmesartan Medoxomil.

How to take

Adult dose

This medication is taken once daily at 1 tablet, with or without food. It is recommended to take it at the same time every day (e.g., in the morning) if possible. The recommended dosage is as follows: - 5/20/12.5 mg: Administered to patients whose blood pressure is not adequately controlled with the combination therapy of Amlodipine/Olmesartan Medoxomil 5/20 mg. - 5/40/12.5 mg: Administered to patients whose blood pressure is not adequately controlled with the combination therapy of Amlodipine/Olmesartan Medoxomil 5/40 mg.

Child dose

The safety and efficacy of this medication have not been established in patients under 18 years of age, and its use is not recommended.

Precautions

This medication should not be used during the second and third trimesters of pregnancy, as taking this drug during pregnancy can cause severe harm or even death to the fetus or newborn. Patients with allergies or hypersensitivity to the components of this drug or similar classes of drugs should not take it. Additionally, women who are pregnant or breastfeeding, patients with severe hypotension, and patients with heart or kidney problems may be at risk if they use this medication. Patients with low blood volume or reduced sodium levels may experience hypotension when initially taking this drug, so caution is required. Such patients should closely monitor their condition before starting treatment and may need fluid therapy if necessary. Patients with impaired kidney function, weakened liver function, specific heart diseases, or systemic lupus erythematosus should be especially cautious when using this medication. As this drug lowers blood pressure, dizziness or lightheadedness may occur. Care should be taken when driving or operating machinery. During the course of taking this medication, electrolyte levels in the blood, especially potassium and sodium levels, should be regularly checked. Electrolyte imbalances may lead to symptoms such as muscle weakness, cramps, and heart irregularities, necessitating caution. This drug may interact with other medications, so it is important to inform a doctor or pharmacist, especially if taking lithium, nonsteroidal anti-inflammatory drugs (NSAIDs), or other antihypertensives. Women who are breastfeeding are advised to avoid using this drug and may need to discontinue breastfeeding if unavoidable. The safety and efficacy of this medication have not been established in children under 18 years of age, and its use is not recommended. For the elderly, dosage adjustments should be made carefully, taking into account liver or kidney function decline. In case of overdose, symptoms such as hypotension, palpitations, and bradycardia may occur, requiring immediate medical attention. This medication should be stored in a tightly sealed container to protect it from light and moisture, and out of the reach of children.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), severe allergic reactions, severe rash with high fever, blisters, skin peeling, pain in the mucous membranes of the mouth/eyes, severe skin adverse reactions, difficulty breathing or shortness of breath, asthma attacks, respiratory issues accompanied by cough and fever, jaundice, liver abnormalities, sudden and extremely severe headaches, lightning headaches, seizures, confusion, visual disturbances, paralysis, severe neurological symptoms, significantly reduced urine output.

Mild side effects

  • Peripheral edema
  • headache
  • dizziness
  • upper respiratory infection
  • nasopharyngitis
  • urinary tract infection
  • sialadenitis
  • leukopenia
  • thrombocytopenia
  • bone marrow suppression
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  • neutropenia/agranulocytosis
  • hemolytic anemia
  • aplastic anemia
  • drug hypersensitivity reactions
  • hyperkalemia
  • hypokalemia
  • loss of appetite
  • diabetes
  • hypercalcemia
  • hyperglycemia
  • hypomagnesemia
  • hyponatremia
  • hypochloremia
  • hypertriglyceridemia
  • hypercholesterolemia
  • hyperuricemia
  • hypochloremic metabolic alkalosis

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

Storage

This medication should be stored in a tightly sealed container to prevent air or moisture from entering. Additionally, it is important to store the medication at room temperature between 1 and 30 degrees Celsius to maintain its effectiveness.

Appearance and packaging

Appearance

Gray-red, round film-coated tablet

Package unit

30 tablets/PTP [10 tablets/Alu-Alu×3]

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.