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LACIPIL TABLET 4 mg

Prescription Only
Drug type: Therapeutic
ATC code: C08CA09
Dosage form: TABLET, FILM COATED
Route of administration: ORAL
Active ingredient: LACIDIPINE; LACIDIPINE

Indications

As a treatment of hypertension either alone or in combination with other antihypertensive agents, e.g. beta-blockers, diuretics and ACE inhibitors.

Contraindications

  • Hypersensitivity to any component of the preparation.

  • As with other dihydropyridines, LACIPIL is contraindicated in patients with severe aortic stenosis.

Dosage and Administration

The initial dosage is 2 mg once daily. It should be taken at the same time each day, preferably in the morning, with or without food.

The treatment of hypertension should be adapted to the severity of the condition, and according to individual response.

The dose may be increased to 4 mg and if necessary to 6 mg, after adequate time has been allowed for the full pharmacological effect to occur. In practice this should not be less than three to four weeks, unless the clinical condition requires a more rapid upward titration.

Treatment may be continued indefinitely.

  • Hepatic impairment

    No dose modification is required in patients with mild or moderate hepatic impairment. Insufficient data are available to make a recommendation for patients with severe hepatic impairment (see Warnings and Precautions – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).

  • Renal impairment

    As lacidipine is not excreted by the kidneys the dose does not require modification in patients with renal impairment.

  • Children

    No experience has been gained with lacidipine in children.

  • Elderly

    No dose modification is required.

Registrant
GLAXOSMITHKLINE PTE LTD
Approval Date
1994-11-25
Approval Number
SIN07934P
Manufacturer
GLAXO WELLCOME SA
Licence Holder
GLAXOSMITHKLINE PTE LTD