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HSA Approval

PURINETONE TABLETS 50 mg

SIN10810P

PURINETONE TABLETS 50 mg

PURINETONE TABLETS 50 mg

March 17, 1999

SHOEI UNIVERSAL CORPORATION PTE LTD

SHOEI UNIVERSAL CORPORATION PTE LTD

Regulatory Information

SHOEI UNIVERSAL CORPORATION PTE LTD

SHOEI UNIVERSAL CORPORATION PTE LTD

Therapeutic

Prescription Only

Formulation Information

TABLET

**DOSAGE AND ADMINISTRATIONS** For adults and children the usual dose is 2.5 mg/kg bodyweight per day, but the dose and duration of administration depend on the nature and dosage of other cytotoxic agents given in conjunction with Mercaptopurine. The dosage should be carefully adjusted to suit the individual patient. Mercaptopurine has been used in various combination therapy schedules for acute leukemia and the literature should be consulted for details. Consideration should be given to reducing the dosage in patients with impaired hepatic or renal function. When allopurinol and mercaptopurine are administered concomitantly it is essential that only a quarter of the usual dose of mercaptopurine is given since allopurinol decreases the rate of catabolism of mercaptopurine.

ORAL

Medical Information

**INDICATIONS** Mercaptopurine is indicated for treatment or maintenance therapy in acute leukemia, acute lymphoblastic leukemia, and acute myelogenous leukemia. Mercaptopurine is also used in the treatment of chronic granulocytic leukemia.

**CONTRAINDICATIONS** 1. Purinetone should not be used in patients who have a hypersensitivity to mercaptopurine or any component of the formulation. 2. Purinetone contains lactose and should not be taken by patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption.

L01BB02

mercaptopurine

Manufacturer Information

SHOEI UNIVERSAL CORPORATION PTE LTD

KOREA UNITED PHARMACEUTICAL INC

Active Ingredients

MERCAPTOPURINE

50 mg

Mercaptopurine

Documents

Package Inserts

Purinetone Tabs 50mg PI.pdf

Approved: March 24, 2021

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