Viewing nowTamulsin Extended-Release Tablet (Tamsulosin Hydrochloride)
Tamsulosin Hydrochloride 0.2mg
Tablet · Prescription medication
Huons Co., Ltd.

MFDS item code 201603317 · Approved 2016.06.09 · Insurance code 670607510
Improvement of urinary symptoms associated with benign prostatic hyperplasia
Urination disorders caused by benign prostatic hyperplasia primarily include symptoms such as difficulty urinating or the sensation of residual urine. This medication is used to alleviate these urination problems related to prostatic hyperplasia and to assist in normal urination.
Adults: Administer 0.2 mg of tamsulosin hydrochloride orally once daily after a meal. Swallow this medicine whole; do not crush or chew it. Adjust the dose as appropriate according to symptoms.
This medication should not be administered to certain patients. Patients who have had allergic reactions to this medication or its components, those with symptoms of orthostatic hypotension, patients with severe liver dysfunction, pregnant women or those who may become pregnant, and patients with lactose intolerance or certain genetic metabolic disorders should avoid taking this medication. Additionally, caution is needed when using this medication in patients with severely impaired kidney function, elderly patients, and those taking specific antihypertensive medications, alpha-1 blockers, PDE5 inhibitors, or CYP3A4 inhibitors. Various side effects may occur during the course of taking this medication, such as dizziness, blood pressure drop, heart-related abnormal symptoms, gastrointestinal discomfort, or skin rash; if any unusual symptoms appear, consult a doctor immediately. In cases of overdose, there is a risk of excessively low blood pressure, so it is important to adhere to the prescribed dosage, especially paying attention to changes in blood pressure during position changes. This medication assists in alleviating symptoms but is not a treatment for the underlying cause, so if symptoms do not improve, other treatment options should be considered. Care should be taken when engaging in hazardous activities such as driving or working at heights, as there is a risk of accidents due to side effects such as dizziness. This medication may cause eye-related complications during certain surgeries, so patients scheduled for ophthalmic surgery should inform their healthcare provider. This medication contains lactose, so lactose-intolerant patients should take it with caution, and caution is also advised for patients with a history of allergic reactions to sulfonamides. The safety of this medication has not been established in pregnant women, nursing mothers, or children under 18, so they should not use this medication. For the elderly, who may have reduced kidney function, treatment should start at a lower dose and be monitored. This medication should be swallowed whole as directed, and it should not be crushed or chewed, as this may alter its efficacy. Finally, keep this medication out of the reach of children and do not transfer it to other containers for safety.
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to air and moisture, so it should be stored in a tightly sealed container. It is recommended to maintain a storage temperature between 1°C and 30°C. This will help preserve the effectiveness of the medication for a longer period.
White round film-coated tablet
30 tablets/bottle, 100 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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.
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For anything that needs medical judgment, consult a doctor or pharmacist.
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.