Lercastad 10

Lercanidipine is a calcium antagonist of the dihydropyridine group and inhibits the transmembrane influx of calcium into cardiac and smooth muscle. Since the vasodilatation induced by lercanidipine hydrochloride is gradual in onset, acute hypotension with reflex tachycardia has rarely been observed in hypertensive patients.

Pack size Box of 30 tablets, 60 tablets
Shelf-life 36 months
Composition Lercanidipine hydrochloride
Dosage forms and strengths Film-coated tablet: 10 mg.
Product code :



Treatment of mild to moderate essential hypertension.


  • The recommended dosage is 10 mg once daily, increased if necessary, after at least 2 weeks, to 20 mg daily.
  • Use in the elderly: Special care should be exercised when initiating treatment in the elderly.
  • Use in renal or hepatic dysfunction: Special care should be exercised when treatment is commenced in patients with mild to moderate renal or hepatic dysfunction. Although the usually recommended dose schedule may be tolerated by these subgroups, an increase in dose to 20 mg daily must be approached with caution. The antihypertensive effect may be enhanced in patients with hepatic impairment and consequently an adjustment of the dosage should be considered.


Lercastad 10 is administered orally at least 15 minutes before meals.

Hypersensitivity to lercanidipine, to any dihydropyridine or to any of the excipients.

Women of child-bearing potential unless effective contraception is used. Pregnancy and lactation.

Left ventricular outflow tract obstruction. Untreated congestive cardiac failure.

Unstable angina pectoris. Within 1 month of a myocardial infarction.

Co-administration with strong inhibitors of CYP3A4, cyclosporin, grapefruit juice.

Patients with severe hepatic impairment or in patients with severe renal impairment (GFR < 30 ml/min).

Patients under the age of 18 years.

Uncommon: Headache, dizziness, peripheral oedema, tachycardia, palpitations, flushing.

Rare: Somnolence, angina pectoris, nausea, dyspepsia, diarrhea, abdominal pain; vomiting, rash, myalgia, polyuria, asthenia, fatigue.

Special care should be exercised when lercanidipine is used in patients with sick sinus syndrome (if a pacemaker is not in situ), in patients with left ventricular dysfunction. It has been suggested that some short-acting dihydropyridines may be associated with increased cardiovascular risk in patients with ischaemic heart disease. Although lercanidipine is long-acting caution is required in such patients.

Patients should be aware of how they react to drug before driving or operating machinery.