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HSA Approval

DHASOLONE TABLET 5 mg

SIN04207P

DHASOLONE TABLET 5 mg

DHASOLONE TABLET 5 mg

April 16, 1990

TEVA PHARMACEUTICAL INVESTMENTS SINGAPORE PTE. LTD.

TEVA PHARMACEUTICAL INVESTMENTS SINGAPORE PTE. LTD.

Regulatory Information

TEVA PHARMACEUTICAL INVESTMENTS SINGAPORE PTE. LTD.

TEVA PHARMACEUTICAL INVESTMENTS SINGAPORE PTE. LTD.

Therapeutic

Prescription Only

Formulation Information

TABLET

**RECOMMENDED DOSES:** Orally administered: Dosage requirements are variable and must be individualized on the basis of the disease under treatment and the response of the patient. Adults : 5–60 mg daily in divided doses or as a single daily or double dose on alternate days. In long term therapy, dosage should be maintained at not more than 7 mg daily whenever possible. Children: As directed by physician. For short term treatment of not more than 2 weeks, as it may lead to growth retardation in children.

ORAL

Medical Information

**INDICATIONS:** For the suppression of inflammatory and allergic disorders and for the treatment of conditions for which corticosteroid therapy is indicated except in adrenal-deficiency states.

**CONTRA-INDICATIONS:** Patients with active or doubtfully quiescent tuberculosis. In the presence of acute infections, including herpes zoster and herpes simplex, ulceration of the eye. Patients with peptic ulcer, osteoporosis, pyschoses or severe psychoneuroses.

H02AB06

prednisolone

Manufacturer Information

TEVA PHARMACEUTICAL INVESTMENTS SINGAPORE PTE. LTD.

PT Actavis Indonesia

Active Ingredients

Prednisolone Base Micronized

5 mg

Prednisolone

Documents

Package Inserts

Att 6 AAAM6055 Dhasolone PI P Clean.pdf

Approved: March 16, 2021

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