Medication info
Lozatine Plus Tablet

Lozatine Plus Tablet

Prescription medicationTablet경구
Ingredient · strength
Losartan Potassium›50mg / 1 tabletHydrochlorothiazide›12.5mg / 1 tablet
Manufacturer / importer
에이치엘비제약(주)
Appearance
Yellow oval film-coated tablet
Packaging
30 tablets/bottle, 300 tablets/bottle
Approval status
Active

MFDS item code 200607957 · Notified 2006.10.16 · Insurance code 647300260

Summary

Main use
Improvement in blood pressure control for hypertension not adequately managed with monotherapy
Who takes it
Adults · Children
Adult dose
Losartan Potassium 50 mg/Hydrochlorothiazide 12.5 mg once daily, 1 tablet. If blood pressure is not adequately controlled, the dose may be increased, with a maximum dose of Losartan Potassium 100 mg/Hydrochlorothiazide 25 mg once daily, 1 tablet. This medication can be taken regardless of meals and is initiated when monotherapy is insufficient in effect.
Child dose
Due to lack of experience in pediatric and adolescent use, the losartan-hydrochlorothiazide combination is not administered to children and adolescents.

Ingredients

Manufacturer
에이치엘비제약(주)

Efficacy & effects

Improvement in blood pressure control for hypertension not adequately managed with monotherapy

  • Hypertension
View approved original text

This medication is used to effectively lower and manage the blood pressure of hypertension patients whose blood pressure is not adequately controlled with monotherapy.

How to take

Adult dose

Losartan Potassium 50 mg/Hydrochlorothiazide 12.5 mg once daily, 1 tablet. If blood pressure is not adequately controlled, the dose may be increased, with a maximum dose of Losartan Potassium 100 mg/Hydrochlorothiazide 25 mg once daily, 1 tablet. This medication can be taken regardless of meals and is initiated when monotherapy is insufficient in effect.

Child dose

Due to lack of experience in pediatric and adolescent use, the losartan-hydrochlorothiazide combination is not administered to children and adolescents.

Precautions

This medication can cause serious harm to the fetus if taken during pregnancy, especially in the second and third trimesters; therefore, it should be discontinued immediately upon confirmation of pregnancy. This medication should not be administered to patients with certain diseases or conditions, such as those with severely impaired kidney function, severe liver impairment, or allergies, as it may pose risks. Patients with low blood pressure or electrolyte imbalances, those with gout or hyperuricemia, and the elderly require special caution when using this medication. While taking this medication, regular blood tests to monitor electrolytes and kidney function should be conducted, paying particular attention to ensure potassium levels do not become too high or too low. This medication may cause side effects such as dizziness, cough, skin rash, muscle pain, and dyspepsia, and in severe cases, serious reactions such as angioedema or cardiac arrhythmias may occur, so patients should consult a doctor immediately if any unusual symptoms arise. Additionally, this medication may interact with certain drugs, so it is essential to inform the doctor or pharmacist if other medications are being taken. Containing hydrochlorothiazide, this medication may increase skin sensitivity to sunlight, so it is recommended to avoid sun exposure and use sunscreen as needed. There is a possibility of dizziness or drowsiness while driving or operating machinery, so caution is advised, especially during the initial stages of treatment or when doses are changed. This medication is not to be used in children, and breastfeeding women should either discontinue breastfeeding or stop using this medication. Finally, this medication should be stored out of reach of children and kept sealed in its original container for safety.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), angioedema (swelling of the lips and eyelids and facial rash), chest tightness, difficulty breathing, acute respiratory distress syndrome (ARDS), shortness of breath or difficulty breathing, asthma attack, respiratory abnormalities accompanied by cough and fever, yellowing of the skin or eyes (jaundice), profound lethargy, jaundice (cholestatic jaundice), sudden and severe headache, seizures, confusion of consciousness, visual disturbances

Mild side effects

  • Abdominal pain
  • swelling
  • palpitations
  • back pain
  • dizziness
  • cough
  • sinusitis
  • upper respiratory infection
  • weakness/fatigue
  • diarrhea
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  • nausea
  • headache
  • bronchitis
  • pharyngitis
  • chest pain
  • facial swelling
  • fever
  • orthostatic hypotension
  • syncope
  • angina
  • arrhythmia
  • hypotension
  • loss of appetite
  • constipation
  • toothache
  • dry mouth
  • dyspepsia
  • flatulence
  • gastritis
  • vomiting
  • malaise
  • anemia
  • gout
  • arm pain
  • joint pain
  • arthritis
  • fibromyalgia
  • hip pain
  • joint swelling
  • knee pain

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

Storage

This medication is sensitive to light, so it should be stored in an opaque container. Additionally, to safeguard the medication, it is best to store it at room temperature, that is, between 1 degree and 30 degrees Celsius.

Appearance and packaging

Appearance

Yellow oval film-coated tablet

Package unit

30 tablets/bottle, 300 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

No questions yet.

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.