Viewing nowTamsulosin Sustained Release 0.2 mg (Tamsulosin Hydrochloride)
Tamsulosin Hydrochloride 0.2mg
Tablet · Prescription medication
CMG Pharmaceutical Co., Ltd.

MFDS item code 201403956 · Approved 2014.08.25 · Insurance code 648602710
Improvement of voiding dysfunction due to benign prostatic hyperplasia
Used to relieve the symptoms of urinary disorders caused by benign prostatic hyperplasia.
Adults: Administer tamsulosin hydrochloride 0.2 mg orally once daily after a meal. Swallow this medication whole; do not crush or chew it. Adjust the dose as appropriate according to symptoms.
This medication should not be used in certain patients. For example, patients who are allergic to this medication or its components, have a history of angioedema, have symptoms of orthostatic hypotension, have severe liver dysfunction, are pregnant or possibly pregnant women, and those with lactose intolerance or specific genetic disorders should not take this medication. Additionally, patients with severely impaired kidney function, the elderly, and patients taking certain antihypertensives or other medications should use this medication cautiously. In particular, patients currently taking alpha-1 blockers should not use this medication in principle, but may use it carefully only when absolutely necessary. This medication can lower blood pressure, which may lead to cardiovascular adverse reactions such as dizziness, orthostatic hypotension, palpitations, and arrhythmias. Neurological and psychiatric symptoms such as headaches, drowsiness, insomnia, and decreased libido have also been reported. If skin rash, itching, or hives occur, discontinue use immediately. In the gastrointestinal system, symptoms such as nausea, vomiting, anorexia, constipation, and diarrhea may occur, and rare cases of liver dysfunction or jaundice may need attention. Rarely, serious side effects such as priapism have been reported, so if such symptoms occur, consult a doctor immediately. This medication may interact with antihypertensives, PDE5 inhibitors, CYP3A4 inhibitors, so inform your doctor or pharmacist if you are taking other medications. It is not used in pregnant or breastfeeding women, or in children under 18, as safety and efficacy have not been established. In the elderly, dosing should start at a lower dose considering the potential for renal impairment, with monitoring of the patient's condition. When taking this medication, take it directly from the packaging, and be careful not to chew or open the capsule. Especially as it is in sustained-release form, the effect of the medication can vary. This medication should be kept out of the reach of children and should not be transferred to another container. Finally, this medication helps alleviate symptoms but does not treat the underlying cause; if symptoms do not improve, consider other treatment options.
Not everyone experiences these, and they can vary from person to person.
Store this medication in a closed container to prevent air or moisture from entering. It is best to keep the storage temperature between 1 to 30 degrees Celsius at room temperature.
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.