Product image of Manyper (Manidipine Dihydrochloride) supplied by GNH India

Manyper

Active Ingredient:
Manidipine Dihydrochloride
Origin:
EU

Manyper (Manidipine Dihydrochloride)

Manidipine, the active ingredient in Manyper, is a calcium channel blocker presented as an oral tablet for oral use. It treats essential hypertension in adult patients by lowering blood pressure and reducing cardiovascular risk.

GNH India supplies Manyper as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Chiesi Hellas S.A.

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Indications & Clinical Uses

  • Manidipine is a dihydropyridine calcium channel blocker indicated for the management of essential hypertension.
  • Essential hypertension: lowers systemic vascular resistance, helping to achieve target blood pressure and reduce the risk of cardiovascular events.

How It Works

  • Manidipine selectively blocks L‑type calcium channels in vascular smooth muscle, inhibiting calcium influx. This causes dose‑dependent vasodilation of peripheral arteries, decreasing peripheral vascular resistance and consequently lowering arterial blood pressure without significant negative inotropic effects.

Side Effects

Manidipine may cause a range of adverse reactions. Patients should be informed of common and serious possibilities.

Common Side Effects

  • Headache: mild to moderate intensity, often transient.
  • Flushing: warm sensation and redness, usually resolves with continued therapy.
  • Peripheral edema: swelling of ankles or feet, may require monitoring.
  • Dizziness: especially upon standing, related to blood pressure reduction.
  • Nausea: occasional gastrointestinal discomfort.
  • Tachycardia: increased heart rate in some individuals.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Myocardial infarction: rare occurrence, especially in patients with pre‑existing coronary disease.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Arrhythmias: abnormal heart rhythms, including ventricular ectopy.
  • Acute kidney injury: sudden decline in renal function.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Renal impairment: assess renal function and monitor for fluid retention.
  • Hepatic impairment: use with caution; monitor liver enzymes.
  • Concomitant antihypertensives: adjust therapy to avoid excessive hypotension.
  • Pregnancy: safety not established; avoid unless clearly needed.
  • Elderly patients: start at lower dose and monitor for orthostatic hypotension.
  • Store at room temperature: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Manidipine may interact with several drug classes, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase plasma concentrations.
  • Other calcium channel blockers: additive vasodilatory effect leading to profound hypotension.
  • Grapefruit juice: can elevate drug exposure and risk of side effects.

Moderate Interactions (Monitor Closely):\n- Diuretics: enhanced antihypertensive effect, monitor electrolytes.

  • Beta‑blockers: possible bradycardia; observe heart rate.
  • ACE inhibitors or ARBs: monitor renal function and potassium levels.

Frequently Asked Questions

Manyper contains manidipine dihydrochloride and is prescribed to lower high blood pressure in adults with essential hypertension. By reducing vascular resistance, it helps achieve target blood pressure levels and lowers the risk of cardiovascular complications.

Manidipine selectively blocks L‑type calcium channels in arterial smooth muscle. This inhibition prevents calcium entry, causing the vessels to relax and dilate, which decreases peripheral vascular resistance and results in lowered systemic blood pressure.

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

Safety of manidipine in pregnancy and lactation has not been established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

To order Manyper, 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.

Manidipine belongs to the dihydropyridine calcium‑channel blocker class, similar to amlodipine. Compared with amlodipine, manidipine may have a slightly lower incidence of peripheral edema, but both provide effective blood‑pressure reduction. Choice of therapy depends on patient tolerance, comorbidities, and physician preference.

Manyper tablets should be stored at room temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

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

Serious risks include severe hypotension, which can cause fainting or shock, and rare cases of myocardial infarction, hepatic dysfunction, or severe allergic reactions such as anaphylaxis. Patients should seek immediate medical attention if they experience symptoms like chest pain, sudden weakness, or difficulty breathing.

Manyper is contraindicated in patients with known hypersensitivity to manidipine or any component of the formulation, and it should be avoided in individuals with severe aortic stenosis or uncontrolled heart failure. Caution is also advised for patients with significant liver or kidney disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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