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PROSCAR TABLET 5 mg

Prescription Only
Drug type: Therapeutic
ATC code: G04CB01
Dosage form: TABLET, FILM COATED
Route of administration: ORAL
Active ingredient: FINASTERIDE; FINASTERIDE

INDICATIONS

  • PROSCAR is indicated for the treatment and control of benign prostatic hyperplasia (BPH) and for the prevention of urologic events as it:
    • May reduce the risk of acute urinary retention
    • May reduce the risk of surgery including transurethral resection of the prostate (TURP) and prostatectomy.
  • PROSCAR causes regression of the enlarged prostate, improves urinary flow and improves the symptoms associated with BPH.

Patients with an enlarged prostate are the appropriate candidates for therapy with PROSCAR.

CONTRAINDICATIONS

PROSCAR is not indicated for use in women or children.

PROSCAR is contraindicated in the following:

  • Hypersensitivity to any component of this product.

  • Pregnancy – Use in women when they are or may potentially be pregnant (see PRECAUTIONS: PREGNANCY and EXPOSURE TO FINASTERIDE – RISK TO MALE FETUS – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).

DOSAGE AND ADMINISTRATION

The recommended dosage is one 5 mg tablet daily with or without food.

DOSAGE IN RENAL INSUFFICIENCY

No adjustment in dosage is required in patients with varying degrees of renal insufficiency (creatinine clearances as low as 9 mL/min) as pharmacokinetic studies did not indicate any change in the disposition of finasteride.

DOSAGE IN THE ELDERLY

No adjustment in dosage is required although pharmacokinetic studies indicated the elimination of finasteride is somewhat decreased in patients more than 70 years of age.

Registrant
ORGANON SINGAPORE PTE. LTD.
Approval Date
1993-10-04
Approval Number
SIN07513P
Manufacturer
AIAC International Pharma, LLC PT. Organon Pharma Indonesia Tbk (Primary and Secondary Packager)
Licence Holder
ORGANON SINGAPORE PTE. LTD.