Medication info
Terazol Tablet 2 mg (Terazosin Hydrochloride)

Terazol Tablet 2 mg (Terazosin Hydrochloride)

Prescription medicationTablet경구
Ingredient · strength
Terazosin Hydrochloride Hydrate›2.374mg / 1 tablet
Manufacturer / importer
아주약품(주)
Appearance
Light orange round tablet
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 200300708 · Notified 2003.10.16 · Insurance code 654003960

Summary

Main use
Improvement of urinary disorders and hypertension due to benign prostatic hyperplasia
Who takes it
Adults
Adult dose
1. Urinary disorders due to benign prostatic hyperplasia - Initial dose: 1mg of terazosin hydrochloride taken orally before bedtime; do not exceed this dose. - Maintenance dose: Slowly increase until symptoms improve, taking 5-10mg orally once a day. - If used in conjunction with diuretics or other antihypertensives, reduce the dosage and increase if needed. 2. Hypertension - Initial dose: 1mg of terazosin hydrochloride taken orally before bedtime.

Ingredients

Manufacturer
아주약품(주)

Efficacy & effects

Improvement of urinary disorders and hypertension due to benign prostatic hyperplasia

  • Urinary disorders
  • hypertension
View approved original text

This medication is used in the treatment of urinary disorders caused by benign prostatic hyperplasia and mild to moderate hypertension.

How to take

Adult dose

1. Urinary disorders due to benign prostatic hyperplasia - Initial dose: 1mg of terazosin hydrochloride taken orally before bedtime; do not exceed this dose. - Maintenance dose: Slowly increase until symptoms improve, taking 5-10mg orally once a day. - If used in conjunction with diuretics or other antihypertensives, reduce the dosage and increase if needed. 2. Hypertension - Initial dose: 1mg of terazosin hydrochloride taken orally before bedtime.

Precautions

This medication should not be used in patients with an allergy or hypersensitivity to certain alpha-blockers. It should not be administered to children under the age of 12. This medication contains lactose; therefore, it should not be given to patients with lactose intolerance or specific genetic metabolic disorders. Patients with severely impaired liver or kidney function need to be cautious when using this medication. Patients with certain conditions such as orthostatic hypotension, heart disease, cerebrovascular disease, or diabetes should use this medication carefully. Caution is also necessary if allergic to Yellow No. 4 (tartrazine) included in this product. This medication may cause side effects such as dizziness, drowsiness, headache, and palpitations, and particular care should be taken when starting or changing the dosage. There may be a risk of fainting due to orthostatic hypotension, so movements should be slow when getting up suddenly after taking the medication. It is advisable to avoid driving or operating heavy machinery when initially taking this medication or changing the dosage. This medication is used for the treatment of prostate hypertrophy but must confirm the absence of cancer before treatment to differentiate from prostate cancer. Patients planning cataract surgery should inform their ophthalmologist of their use of this medication. There are generally few interactions with other drugs, but caution should be exercised when taken with antihypertensive agents as it may lower blood pressure excessively. Women who are pregnant or may become pregnant should use this medication carefully, and nursing mothers are advised to avoid taking it or to stop breastfeeding. For the elderly, start with a low dose and observe their condition before administering further. In case of overdose, acute hypotension may occur; immediate medical attention is required as dialysis is ineffective. This medication should be kept out of reach of children and should not be transferred to another container.

Side effects and when to seek care immediately

Serious side effects

Fainting, severe allergic reactions (hives, severe swelling, chest tightness, difficulty breathing, cold sweat, pallor), respiratory distress, severe edema or urinary abnormalities (significantly reduced urine output, severe generalized swelling, high blood pressure), liver abnormalities (yellowing of skin or eyes, extreme lethargy), severe neurological symptoms (sudden and severe headaches, thunderclap headaches, seizures, confusion, visual disturbances, paralysis)

Mild side effects

  • Dizziness
  • energy depletion
  • peripheral edema
  • depression
  • nervousness
  • headache
  • lethargy
  • weakness
  • sweating
  • insomnia
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  • cold sensation
  • shoulder stiffness
  • drowsiness
  • thirst
  • numbness
  • tachycardia
  • vasodilation
  • orthostatic dysregulation
  • palpitations
  • edema
  • arrhythmia
  • chest pain
  • angina
  • elevated AST
  • ALT
  • ALP
  • total bilirubin
  • dyspepsia
  • abdominal bloating
  • diarrhea
  • abdominal pain
  • constipation
  • nausea
  • vomiting
  • loss of appetite
  • epistaxis
  • influenza symptoms.

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

Storage

This medication must be stored in a tightly sealed container to prevent exposure to air or moisture. It is important to maintain the storage temperature between 1 and 30 degrees Celsius. Doing so will help preserve the effectiveness and safety of the medication.

Appearance and packaging

Appearance

Light orange round tablet

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.