Medication info

Losarzen Plus Tablets

Prescription medicationTablet경구Expired
Ingredient · strength
Losartan Potassium›50mg / 1 tabletHydrochlorothiazide›12.5mg / 1 tablet
Manufacturer / importer
(주)셀릭스
Appearance
Yellow oval film-coated tablets
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Expired

MFDS item code 201507455 · Approved 2015.10.29

This product's status changed to Expired on 2025.10.29. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improves blood pressure control in cases of insufficient monotherapy for hypertension
Who takes it
Adults · Children
Adult dose
The usual dose of this medication is Losartan potassium 50 mg/Hydrochlorothiazide 12.5 mg, one tablet once a day. Doses exceeding Losartan potassium 100 mg/Hydrochlorothiazide 25 mg per day are not preferred. - For patients whose blood pressure is not controlled with monotherapy using Losartan or Hydrochlorothiazide: start treatment with Losartan potassium 50 mg/Hydrochlorothiazide 12.5 mg, one tablet once a day.
Child dose
There is no experience of use in children and adolescents (under 18 years of age), so this combination should not be administered to children and adolescents.

Ingredients

Manufacturer
(주)셀릭스

Efficacy & effects

Improves blood pressure control in cases of insufficient monotherapy for hypertension

  • Hypertension
View approved original text

This medication is used for patients with hypertension who do not achieve sufficient blood pressure control with monotherapy. It helps effectively manage hypertension and reduce the risk of cardiovascular complications.

How to take

Adult dose

The usual dose of this medication is Losartan potassium 50 mg/Hydrochlorothiazide 12.5 mg, one tablet once a day. Doses exceeding Losartan potassium 100 mg/Hydrochlorothiazide 25 mg per day are not preferred. - For patients whose blood pressure is not controlled with monotherapy using Losartan or Hydrochlorothiazide: start treatment with Losartan potassium 50 mg/Hydrochlorothiazide 12.5 mg, one tablet once a day.

Child dose

There is no experience of use in children and adolescents (under 18 years of age), so this combination should not be 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, so it should be discontinued immediately upon confirmation of pregnancy. Patients allergic to any ingredients in this medication, those with certain kidney and liver dysfunctions, and women of childbearing potential should not take this drug. Patients with low blood pressure, kidney abnormalities, electrolyte imbalances, elderly patients, and those with a history of certain skin cancers should use this medication cautiously. During usage, it is necessary to regularly monitor electrolyte levels in the blood and kidney function to ensure there are no abnormalities. This medication lowers blood pressure, so dizziness or drowsiness may occur at the beginning of treatment or when changing doses, which requires caution while driving or operating machinery. It may interact with other medications; therefore, patients should inform their doctor or pharmacist of all medications they are currently taking, especially potassium supplements or certain diuretics. This medication may be sensitive to sunlight, so precautions should be taken to protect against UV light, and if any unusual skin reactions occur, medical consultation should be sought immediately. Keep out of reach of children and store in the original container to prevent misuse or degradation of quality.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), angioedema (swelling of lips and eyelids and facial rash), chest tightness, difficulty breathing, angioedema (could cause airway obstruction from laryngeal/glottic swelling, swelling of the face/lips/pharynx/tongue), cold sweat, pallor, severe rash with fever, blisters, skin peeling, oral/ocular mucosal pain, yellowing of the skin or eyes (jaundice), severe lethargy, skin and mucous membrane syndrome (Stevens-Johnson syndrome)

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
  • peeling skin of the palms
  • hemolysis
  • chest pain
  • facial swelling
  • fever
  • orthostatic hypotension
  • fainting
  • angina
  • arrhythmia
  • cerebrovascular accident
  • hypotension
  • myocardial infarction
  • secondary AV block
  • loss of appetite
  • constipation
  • toothache
  • dry mouth
  • dyspepsia
  • flatulence
  • gastritis
  • vomiting
  • lethargy
  • anemia

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

Storage

This medication is sensitive to light and should be stored in a container that does not allow light to enter. It should also be stored at room temperature between 1 and 30 degrees Celsius, avoiding very hot or cold places. This will help maintain the medication's effectiveness over time.

Appearance and packaging

Appearance

Yellow oval film-coated tablets

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.