Product image of Lerdip (Lercanidipine Hydrochloride) supplied by GNH India

Lerdip

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lerdip (Lercanidipine Hydrochloride)

Lercanidipine Hydrochloride, the active ingredient in Lerdip, is a calcium channel blocker presented as an oral tablet for oral administration. It works by relaxing vascular smooth muscle, thereby lowering systemic arterial pressure and is used in the treatment of hypertension in adult patients.

GNH India supplies Lerdip as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable access to quality‑assured medicines.

Manufacturer / TM Owner

Recordati Ireland Ltd.

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Indications & Clinical Uses

  • Lerdip is a calcium channel blocker that acts on the cardiovascular system to control elevated blood pressure.
  • Essential hypertension: reduces both systolic and diastolic blood pressure.
  • Isolated systolic hypertension: lowers elevated systolic pressure in older adults.
  • Secondary hypertension (when appropriate): assists in achieving target blood pressure alongside other therapies.

How It Works

  • Lercanidipine hydrochloride selectively inhibits L-type calcium channels in vascular smooth muscle cells. By blocking calcium influx, it prevents contraction of arterial smooth muscle, leading to vasodilation of peripheral arteries. This reduction in peripheral vascular resistance results in a decrease in systemic blood pressure, helping to control hypertension.

Side Effects

Lercanidipine may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Flushing: transient warmth and redness of the skin.
  • Peripheral edema: swelling of the ankles or feet.
  • Dizziness or light‑headedness, especially on standing.
  • Tachycardia: increased heart rate.
  • Fatigue or general weakness.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips, tongue, or throat.
  • Severe hypotension: marked drop in blood pressure leading to fainting.
  • Myocardial infarction: rare occurrence of heart attack.
  • Hepatic enzyme elevation: abnormal liver function tests.
  • Allergic reactions: rash, itching, or hives.
  • Cardiac arrhythmias: irregular heart rhythms.

Precautions & Warnings

Before initiating therapy with Lerdip, certain safety considerations should be observed.

  • Renal impairment: monitor kidney function and adjust therapy if needed.
  • Hepatic impairment: use with caution and observe liver enzymes.
  • Concomitant antihypertensives: watch for additive blood‑pressure lowering effects.
  • Pregnancy: avoid unless the potential benefit justifies the risk.
  • Elderly patients: start at the lowest effective dose and titrate slowly.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Lerdip can interact with several medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase plasma concentrations.
  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic effect.
  • Grapefruit juice: can markedly raise drug levels.

Moderate Interactions (Monitor Closely):\n- Diuretics: risk of excessive blood‑pressure reduction.

  • Beta‑blockers: additive hypotensive effect.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive response.

Frequently Asked Questions

Lerdip contains lercanidipine hydrochloride, a calcium channel blocker prescribed to lower high blood pressure (hypertension) in adult patients. By relaxing arterial smooth muscle, it helps achieve target blood‑pressure levels and reduces cardiovascular risk.

Lercanidipine selectively blocks L‑type calcium channels in vascular smooth‑muscle cells, preventing calcium entry that is necessary for muscle contraction. This inhibition causes arterial vasodilation, decreasing peripheral resistance and ultimately lowering systemic blood pressure.

The appropriate dose of Lerdip is determined by the prescribing healthcare professional based on the individual’s medical condition, response to therapy, and other medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety of lercanidipine in pregnancy has not been established, and it should only be used if the potential benefit outweighs the risk to the fetus. Breastfeeding is not recommended unless the prescriber determines that the advantages for the mother justify potential exposure to the infant.

To request Lerdip, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Lerdip belongs to the dihydropyridine class of calcium channel blockers, offering once‑daily dosing and a favorable side‑effect profile compared with some older agents. Compared with ACE inhibitors or ARBs, it primarily lowers blood pressure through vasodilation rather than affecting the renin‑angiotensin system.

Lerdip should be stored at ambient temperature, below 25 °C, in its original container. Keep the product away from moisture, direct sunlight, and excessive heat to maintain its stability and potency.

Lerdip is taken orally, usually once daily, with or without food, as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious adverse reactions, although rare, include angioedema, severe hypotension, myocardial infarction, significant liver enzyme elevations, and cardiac arrhythmias. Patients should seek immediate medical attention if they experience swelling of the face or throat, fainting, chest pain, or irregular heartbeats.

Lerdip is contraindicated in patients with known hypersensitivity to lercanidipine or any component of the formulation. It should also be avoided in individuals with severe aortic stenosis, unstable angina, or cardiogenic shock, and used with caution in pregnant or breastfeeding women.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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