Product image of Monopin (Lacidipine) supplied by GNH India

Monopin

Active Ingredient:
Lacidipine
Origin:
EU

Monopin (Lacidipine)

Lacidipine, the active ingredient in Monopin, is a dihydropyridine calcium channel blocker presented as an oral formulation for systemic use. It works by relaxing vascular smooth muscle, leading to vasodilation and a reduction in peripheral resistance, thereby lowering elevated blood pressure in adults diagnosed with hypertension.

GNH India supplies Monopin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable access to quality‑assured antihypertensive medication. The company adheres to stringent manufacturing standards and offers comprehensive logistics support for global distribution.

Manufacturer / TM Owner

Pliva Hrvatska D.O.O.

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Indications & Clinical Uses

Lacidipine is indicated for the management of hypertension, a condition characterized by chronically elevated arterial pressure.

  • Hypertension: reduces systolic and diastolic blood pressure, helping achieve target levels.
  • Essential hypertension: provides consistent blood pressure control in patients with primary hypertension.
  • Isolated systolic hypertension: effectively lowers elevated systolic pressure, particularly in older adults.

How It Works

  • Lacidipine selectively blocks L‑type calcium channels in vascular smooth muscle cells. By inhibiting calcium influx, it prevents contraction of arterial smooth muscle, producing dose‑dependent vasodilation. The resulting decrease in peripheral vascular resistance lowers systemic blood pressure without significant effect on cardiac conduction or contractility. The drug exhibits a long half‑life, allowing once‑daily dosing, and its antihypertensive effect is additive when combined with other agents that act on different pathways, such as diuretics or ACE inhibitors.

Side Effects

Lacidipine may be associated with several adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Headache: mild to moderate pain often occurring early in therapy.
  • Flushing: transient warmth and redness of the skin.
  • Peripheral edema: swelling of the ankles or lower limbs.
  • Dizziness: sensation of light‑headedness, especially when standing.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure leading to fainting.
  • Angioedema: rapid swelling of face, lips, tongue or airway.
  • Hepatic dysfunction: abnormal liver enzymes or jaundice.

Precautions & Warnings

When prescribing lacidipine, clinicians should consider several precautionary measures to ensure safe use.

  • Blood pressure monitoring: check readings regularly after initiation and dose adjustments.
  • Liver function assessment: evaluate hepatic enzymes before starting therapy and periodically thereafter.
  • Concomitant antihypertensives: adjust doses of other blood‑pressure drugs to avoid excessive hypotension.
  • Elderly patients: start with the lowest effective dose and monitor for orthostatic effects.
  • Abrupt discontinuation: taper the medication gradually to prevent rebound hypertension.
  • Store at room temperature: keep tablets in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lacidipine can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase lacidipine plasma levels, raising risk of hypotension.
  • Grapefruit juice: can markedly elevate drug concentration and precipitate severe blood pressure drops.
  • Concurrent use with other calcium‑channel blockers: may cause additive vasodilatory effects and profound hypotension.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce lacidipine effectiveness.
  • Beta‑blockers or ACE inhibitors: combined therapy may enhance antihypertensive response, requiring dose titration.
  • Diuretics: may increase risk of electrolyte imbalance and orthostatic hypotension.
  • NSAIDs: can attenuate antihypertensive effect of lacidipine.

Frequently Asked Questions

Monopin contains lacidipine, which is prescribed to lower high blood pressure in adults diagnosed with hypertension. By reducing peripheral vascular resistance, it helps achieve and maintain target blood‑pressure levels and reduces the risk of cardiovascular complications associated with uncontrolled hypertension.

Lacidipine selectively inhibits L‑type calcium channels in the smooth muscle of arterial walls. This blockade prevents calcium‑induced contraction, causing the vessels to relax and dilate. The resulting fall in peripheral resistance lowers systemic blood pressure without markedly affecting heart rate or contractility.

The appropriate dose of Monopin is determined by the prescribing healthcare professional based on the individual’s blood‑pressure profile, age, renal and hepatic function, and concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for lacidipine during pregnancy and lactation are limited. It should only be used if the potential benefit justifies the possible risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.

To request Monopin, 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.

Monopin (lacidipine) belongs to the dihydropyridine calcium‑channel blocker class, which primarily causes arterial vasodilation. Compared with beta‑blockers or ACE inhibitors, it has a lower impact on heart rate and cardiac output but may be more likely to cause peripheral edema. It can be combined with agents from other classes for additive blood‑pressure control.

Monopin tablets should be stored at room temperature, below 25 °C, in the original packaging. Keep them away from excess moisture, heat and direct sunlight. Do not use the product after the expiry date printed on the label.

Monopin is taken orally, usually once daily, with or without food as directed by the prescriber. The tablet should be swallowed whole with a glass of water. Patients should not crush, chew, or split the tablet unless specifically instructed by a healthcare professional.

Serious adverse reactions include severe hypotension, which can cause fainting or dizziness, and angioedema, a rapid swelling of the face, lips, tongue or airway that may threaten breathing. Signs of liver injury such as jaundice or dark urine also require immediate medical attention.

Monopin is contraindicated in patients with known hypersensitivity to lacidipine or any component of the formulation, and in those with severe aortic stenosis or unstable angina. Caution is advised in patients with significant liver impairment, and it should be avoided in individuals taking strong CYP3A4 inhibitors without dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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