Medication info
Neurotan Plus F Tablets

Neurotan Plus F Tablets

Prescription medicationTablet경구
Ingredient · strength
Losartan Potassium›100mg / 1 tabletHydrochlorothiazide›25mg / 1 tablet
Manufacturer / importer
한국유니온제약(주)
Appearance
Light yellow oval film-coated tablets
Packaging
30 tablets/bottle, 300 tablets/bottle
Approval status
Active

MFDS item code 200607908 · Notified 2006.09.13 · Insurance code 665500280

Summary

Main use
Improves blood pressure control when monotherapy is insufficient for hypertension
Who takes it
Adults · Children
Adult dose
The usual adult dosage is 1 tablet of Losartan Potassium 50 mg/Hydrochlorothiazide 12.5 mg once daily. A dosage exceeding Losartan Potassium 100 mg/Hydrochlorothiazide 25 mg per day is not desirable. 1. When blood pressure control is inadequate with monotherapy of Losartan Potassium and Hydrochlorothiazide, it starts at 50 mg/12.5 mg once daily and the blood pressure is checked 3 weeks later.
Child dose
There is no experience of use in pediatric and adolescent patients (under 18 years old), so it is not administered.

Ingredients

Manufacturer
한국유니온제약(주)

Efficacy & effects

Improves blood pressure control when monotherapy is insufficient 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.

How to take

Adult dose

The usual adult dosage is 1 tablet of Losartan Potassium 50 mg/Hydrochlorothiazide 12.5 mg once daily. A dosage exceeding Losartan Potassium 100 mg/Hydrochlorothiazide 25 mg per day is not desirable. 1. When blood pressure control is inadequate with monotherapy of Losartan Potassium and Hydrochlorothiazide, it starts at 50 mg/12.5 mg once daily and the blood pressure is checked 3 weeks later.

Child dose

There is no experience of use in pediatric and adolescent patients (under 18 years old), so it is not administered.

Precautions

This medication may cause severe 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 known allergies to any ingredients included in this drug or to the drug itself, patients with severely impaired renal function, patients with severe hepatic impairment, and women who are pregnant or may become pregnant should not take this medication. Patients with excessively low blood pressure or electrolyte imbalance, those with liver or kidney disease, patients with hyperuricemia or gout, and the elderly should use caution when taking this medication. Due to the hydrochlorothiazide component, the concentration of electrolytes in the body may change, so regular blood tests should be performed to monitor electrolyte status, and extra caution is needed in cases of dehydration, vomiting, or diarrhea. This medication lowers blood pressure, so dizziness or drowsiness may occur at the beginning of treatment or with dosage adjustments; care should be taken when driving or operating machinery. Do not arbitrarily take potassium supplements or medications containing potassium, and it is essential to consult with a doctor or pharmacist due to potential drug interactions with other medications being taken. If allergic symptoms such as rash, swelling, or difficulty breathing occur during use, discontinue use immediately and inform medical personnel. This medication has not been shown to be safe for children, so it is not used in pediatric or adolescent patients. Store this medication out of reach of children, keeping it sealed in its original container.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, peeling skin, pain in oral/ocular mucosa, shortness of breath or difficulty breathing, asthma attack, respiratory issues accompanied by cough and fever, yellowing of skin or eyes (jaundice), profound lethargy, sudden and severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis, urine

Mild side effects

  • Abdominal pain
  • swelling/edema
  • palpitations
  • low 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
  • fainting
  • angina
  • arrhythmia
  • hypotension
  • myocardial infarction
  • secondary AV block
  • lack of appetite
  • constipation
  • toothache
  • dry mouth
  • indigestion
  • flatulence
  • gastritis
  • vomiting
  • malaise
  • anemia
  • gout
  • arm pain
  • joint pain
  • arthritis
  • fibromyalgia

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

Storage

This medication should be kept in a container that does not allow light or air to enter, stored at room temperature between 1 to 30 degrees Celsius. Storing it this way will help maintain its efficacy for a longer time.

Appearance and packaging

Appearance

Light yellow oval film-coated tablets

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.