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Cabergoline (Cabergoline) - Indications and Dosage

 


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INDICATIONS AND USAGE

Cabergoline tablets are indicated for the treatment of hyperprolactinemic disorders, either idiopathic or due to pituitary adenomas.

DOSAGE AND ADMINISTRATION

The recommended dosage of cabergoline tablets for initiation of therapy is 0.25 mg twice a week. Dosage may be increased by 0.25 mg twice weekly up to a dosage of 1 mg twice a week according to the patient's serum prolactin level.

Dosage increases should not occur more rapidly than every 4 weeks, so that the physician can assess the patient's response to each dosage level. If the patient does not respond adequately, and no additional benefit is observed with higher doses, the lowest dose that achieved maximal response should be used and other therapeutic approaches considered.

After a normal serum prolactin level has been maintained for 6 months, cabergoline may be discontinued, with periodic monitoring of the serum prolactin level to determine whether or when treatment with cabergoline should be reinstituted. The durability of efficacy beyond 24 months of therapy with cabergoline has not been established.

HOW SUPPLIED

Cabergoline tablets are white, scored, capsule-shaped tablets containing 0.5 mg cabergoline. Each tablet is scored. The tablet has the letter G engraved on one side, the other side is engraved with the number 100.

Cabergoline is available as follows:

Bottles of 8 tablets                                                          NDC 59762-0100-1

STORAGE

Store at controlled room temperature 20° to 25°C (68° to 77°F) [see USP].

Rx only

LAB-0304-3.0

Page last updated: 2006-03-01

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