Medication info
Jadart Tablet 0.5 mg (Dutasteride)

Jadart Tablet 0.5 mg (Dutasteride)

Prescription medicationTabletOral
Ingredient · strength
Dutasteride›0.5mg / 1 tablet
Manufacturer / importer
JW Pharmaceutical Co., Ltd.
Appearance
Pale yellow oval film-coated tablet
Packaging
30 tablets (10 tablets/PTP x 3)
Approval status
Active

MFDS item code 201802719 · Approved 2018.06.29 · Insurance code 644914500

Summary

Main use
Improvement of benign prostatic hyperplasia (symptoms, urinary retention, risk of surgery); treatment of male-pattern hair loss
Who takes it
Adults
Adult dose
The recommended dose of this medicine is 1 tablet (0.5mg) once daily. Swallow this medicine whole without chewing or splitting it. This medicine may be taken with or without food. No dose adjustment is necessary in patients with renal impairment or elderly patients. Since there are no data on administration of this medicine to patients with hepatic impairment, the recommended dose of this medicine in patients with hepatic impairment has not been established.

Ingredients

Manufacturer
JW Pharmaceutical Co., Ltd.

Efficacy & effects

Improvement of benign prostatic hyperplasia (symptoms, urinary retention, risk of surgery); treatment of male-pattern hair loss

  • Benign prostatic hyperplasia
  • acute urinary retention
  • male pattern hair loss
View approved original text

This medication is used to improve various symptoms caused by benign prostatic hyperplasia. It also reduces the risk of acute urinary retention, helping to decrease the need for prostate-related surgery. Additionally, it is used for the treatment of male pattern hair loss in adult men, contributing to the mitigation of hair loss progression. Therefore, it is effectively used for the treatment of benign prostatic hyperplasia and male pattern hair loss.

How to take

Adult dose

The recommended dose of this medicine is 1 tablet (0.5mg) once daily. Swallow this medicine whole without chewing or splitting it. This medicine may be taken with or without food. No dose adjustment is necessary in patients with renal impairment or elderly patients. Since there are no data on administration of this medicine to patients with hepatic impairment, the recommended dose of this medicine in patients with hepatic impairment has not been established.

Precautions

This medication is absorbed through the skin, so women who are pregnant or may become pregnant should not touch or handle this medication. In particular, it should be avoided to touch broken or damaged pieces of this medication. Children under 18 years of age or women should not use this medication. Men planning to conceive should use this medication cautiously, as it may affect reproductive capacity, based on a doctor's judgment. Patients with urinary issues or liver function abnormalities should use this medication with caution, especially in cases with urinary obstruction symptoms. This medication is extensively metabolized in the liver, so it should be used with caution in patients with liver disorders. Patients taking strong CYP3A4 enzyme inhibitors for a long time may have increased blood concentration when used with this medication, so caution is advised. During the use of this medication, erectile dysfunction, decreased libido, ejaculation disorders, and other sexual dysfunctions may occur, which may persist even after stopping the medication. Additionally, breast-related adverse reactions such as gynecomastia and breast tenderness may occur. Patients receiving this medication should have their PSA levels checked regularly for prostate cancer screening, as this medication lowers PSA levels, requiring caution in interpreting test results. Blood donation should be avoided during the use of this medication, and a minimum of 6 months should pass after the last dose before blood donation is possible. There is no specific antidote for overdose, so appropriate supportive treatment should be administered according to symptoms. Keep this medication out of the reach of children and store it in its original container to prevent misuse or deterioration of quality. This medication is unlikely to affect driving or operating machinery, but caution is necessary as it may vary among individuals. In patients with heart failure, co-administration of this medication with other agents may increase the risk of heart failure, so careful observation is required. No significant drug interactions with several other medications have been reported; however, caution is needed when combined with certain drugs. This medication should not be used by pregnant women or nursing mothers, as it may have serious effects on the fetus. Even with prolonged use, sexual dysfunction or breast disorders may continue to occur, necessitating regular monitoring.

Side effects

  • erectile dysfunction
  • decreased libido
  • ejaculation disorder
  • gynecomastia
  • headache
  • gastrointestinal discomfort and pain
  • sexual dysfunction
  • breast disorders
  • dizziness
  • heart failure
Show 84 more
  • rash
  • itching
  • urticaria
  • localized swelling
  • severe skin reactions
  • angioedema
  • depressed mood
  • alopecia
  • hirsutism
  • testicular pain
  • testicular swelling
  • male breast cancer
  • dyspepsia
  • insomnia
  • abdominal pain
  • diarrhea
  • allergy
  • fever
  • congestion
  • thromboembolic stroke
  • lung cancer
  • pulmonary embolism
  • pneumonia
  • xerostomia
  • constipation
  • spasm
  • orofacial dyskinesia
  • vomiting
  • colorectal polyp
  • epigastric discomfort
  • weakness
  • deep vein thrombosis
  • chills
  • gastroesophageal reflux
  • hemorrhoids
  • pain
  • fatigue
  • increased SGPT
  • rash
  • sexual dysfunction
  • pharyngitis
  • appendicitis
  • fracture
  • viral infection
  • acne
  • fungal dermatitis
  • seborrhea
  • dermatological diseases
  • folliculitis
  • eczema
  • fatty liver
  • chest pain
  • palpitations
  • warts
  • contact dermatitis
  • dry skin
  • peptic ulcer
  • gastritis
  • gastroenteritis
  • drowsiness
  • hyperbilirubinemia
  • upper respiratory tract infection
  • unspecified abrasion
  • surgical intervention
  • laceration
  • hyperuricemia
  • hypertriglyceridemia
  • weight gain
  • sensory abnormalities
  • decreased testosterone
  • skeletal pain
  • plantar fasciitis
  • purpura
  • nosebleed
  • blepharitis
  • benign laryngeal neoplasm
  • kidney stones
  • taste distortion
  • capillary dilatation
  • visual disturbances
  • thirst
  • urinary abnormalities
  • hematuria
  • semen abnormalities

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

Storage

This medication should be stored in a tightly closed container to prevent air or moisture from entering. It is advisable to maintain a storage temperature between 1 to 30 degrees Celsius.

Appearance and packaging

Appearance

Pale yellow oval film-coated tablet

Package unit

30 tablets (10 tablets/PTP x 3)

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.