Product image of Nimotop (Nimodipine) supplied by GNH India

Nimotop

Active Ingredient:
Nimodipine
Origin:
EU

Nimotop (Nimodipine)

Nimodipine, the active ingredient in Nimotop, is a calcium channel blocker presented as a formulation for intracisternal and intravenous use. It is employed to reduce the risk of cerebral vasospasm following subarachnoid hemorrhage and to support neurological recovery.

GNH India supplies Nimotop as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, including tertiary care centers and specialty clinics, with adherence to global quality standards and reliable logistics throughout.

Manufacturer / TM Owner

Laboratoire Xo

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Indications & Clinical Uses

Nimodipine acts on cerebral vascular smooth muscle to prevent vasospasm after subarachnoid hemorrhage.

  • Subarachnoid hemorrhage: prevention of delayed cerebral vasospasm.
  • Aneurysmal subarachnoid hemorrhage: reduction of secondary ischemic injury.
  • Neurovascular protection: supports cerebral blood flow after hemorrhagic events.

How It Works

  • Nimodipine selectively blocks L‑type calcium channels on cerebral arterial smooth muscle, decreasing calcium influx. This preferential vasodilation of cerebral vessels lowers vascular resistance, mitigates vasospasm, and improves perfusion to ischemic brain tissue after subarachnoid hemorrhage.

Side Effects

Nimotop may cause adverse reactions that vary in frequency and severity.

Common Side Effects

  • Headache: mild to moderate pain, often transient.
  • Hypotension: low blood pressure that can cause light‑headedness.
  • Nausea: feeling of stomach upset.
  • Flushing: warm sensation and reddening of the skin.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Cardiac arrhythmia: irregular heart rhythm that may be life‑threatening.
  • Hepatic injury: elevated liver enzymes or jaundice.
  • Anaphylactic reaction: severe allergy with breathing difficulty.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Monitor blood pressure: check regularly for hypotension.
  • Assess liver function: perform baseline and periodic liver enzyme tests.
  • Use caution in cardiac disease: avoid in patients with severe heart failure or conduction disorders.
  • Avoid concurrent potent vasodilators: limit use with other calcium channel blockers or nitrates.
  • Adjust in renal impairment: consider dose modification in severe renal dysfunction.
  • Store at ambient temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

Nimodipine can interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Other calcium channel blockers: additive vasodilatory effect may cause severe hypotension.
  • Potent CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): increase nimodipine plasma concentrations, raising toxicity risk.
  • Nitrates or other vasodilators: combined use can lead to profound blood pressure drops.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may lower nimodipine levels and reduce efficacy.
  • Antihypertensive agents (e.g., ACE inhibitors, ARBs): may enhance blood pressure lowering.
  • Beta‑blockers: can potentiate bradycardia when combined with nimodipine.

Frequently Asked Questions

Nimotop contains nimodipine and is prescribed to prevent cerebral vasospasm after a subarachnoid hemorrhage, helping to maintain adequate blood flow to the brain and reduce the risk of delayed ischemic injury.

Nimodipine selectively blocks L‑type calcium channels in cerebral arterial smooth muscle, causing targeted vasodilation of brain vessels. This reduces calcium‑driven contraction, preventing the narrowing of arteries that can follow a subarachnoid bleed.

The dosage of Nimotop is determined by the treating physician based on the patient’s clinical condition, route of administration, and local guidelines. Only a qualified prescriber can set the appropriate regimen.

Safety data for nimodipine in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by a healthcare professional.

To request Nimotop, 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.

Nimodipine is distinguished by its preferential dilation of cerebral vessels, whereas many other calcium channel blockers primarily affect peripheral vasculature. This neurovascular selectivity makes nimodipine the preferred choice for preventing vasospasm after subarachnoid hemorrhage.

Nimotop should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight, and extreme temperature fluctuations to maintain stability.

Nimotop is supplied for intracisternal or intravenous administration by a qualified healthcare professional. The route and rate of infusion are determined by the prescriber according to the patient’s condition and institutional protocols.

Serious risks include severe hypotension, cardiac arrhythmias, hepatic injury, and anaphylactic reactions. Prompt medical evaluation is required if any of these events occur during therapy.

Patients with known hypersensitivity to nimodipine or any component of the formulation, those with severe uncontrolled hypotension, or individuals with certain cardiac conduction disorders should avoid Nimotop unless a physician determines the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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