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 30 mg oral tablet for oral use. It is indicated for the prevention of cerebral vasospasm following subarachnoid hemorrhage, helping to maintain cerebral blood flow in affected patients.

GNH India supplies Nimotop as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies and clinics worldwide, with a focus on quality assurance and regulatory compliance for EU‑origin medicines and supporting timely delivery across global markets.

Manufacturer / TM Owner

Laboratoire Xo

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Indications & Clinical Uses

Nimotop (nimodipine) is a cerebral vasodilator used in the management of vascular complications after subarachnoid hemorrhage.

  • Subarachnoid hemorrhage: prevention of cerebral vasospasm to reduce the risk of delayed ischemic neurological deficits.
  • Aneurysmal SAH: supports maintenance of cerebral perfusion during the acute phase.
  • Neurocritical care after SAH: adjunct therapy to improve cerebral blood flow and limit secondary brain injury.

How It Works

  • Nimodipine selectively blocks L‑type calcium channels in vascular smooth muscle, especially within cerebral arteries. By inhibiting calcium influx, it induces vasodilation of intracranial vessels, thereby increasing cerebral blood flow and providing neuroprotective effects against ischemic injury following subarachnoid hemorrhage.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate pain often reported during early therapy.
  • Hypotension: transient lowering of blood pressure, especially when standing.
  • Nausea or vomiting: gastrointestinal discomfort that may resolve with continued use.
  • Flushing or warmth: sensation of heat, usually on the face or neck.
  • Dizziness or light‑headedness: related to blood pressure changes.
  • Tachycardia: increased heart rate in some patients.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Myocardial ischemia or infarction: rare cardiac events linked to excessive vasodilation.
  • Hepatic dysfunction: abnormal liver enzymes or jaundice.
  • Allergic reactions: rash, pruritus, or anaphylaxis in hypersensitive individuals.
  • Seizures: infrequent neurologic events reported in isolated cases.

Precautions & Warnings

Before initiating Nimotop, clinicians should consider several safety measures.

  • Blood pressure monitoring: check for hypotension, especially in patients on other antihypertensives.
  • CYP3A4 inhibitors: avoid strong inhibitors (e.g., ketoconazole) that may raise nimodipine levels.
  • Hepatic impairment: use with caution and adjust therapy if liver function is compromised.
  • Abrupt discontinuation: do not stop suddenly without medical guidance to prevent rebound vasospasm.
  • Store at ambient temperature: keep in the original pack, protect from moisture and light.

Avoid Interactions

Nimotop can interact with other medicines, requiring attention to the level of risk.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase plasma concentrations and risk of toxicity.
  • Concomitant antihypertensives: additive hypotensive effect.
  • Grapefruit juice: can elevate nimodipine exposure.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy.
  • Other calcium channel blockers: potential for enhanced cardiovascular effects.
  • Diuretics: may affect electrolyte balance and blood pressure stability.

Frequently Asked Questions

Nimotop contains nimodipine, a calcium channel blocker that is used to prevent cerebral vasospasm after subarachnoid hemorrhage. By keeping the brain’s blood vessels dilated, it helps reduce the risk of delayed ischemic neurological deficits in patients who have suffered this type of bleed.

Nimodipine selectively blocks L‑type calcium channels in the smooth muscle of cerebral arteries. This inhibition reduces calcium entry, causing the vessels to relax and dilate, which improves cerebral blood flow and offers neuroprotection during the critical period after a subarachnoid hemorrhage.

The specific dose of Nimotop is determined by the prescribing clinician based on the patient’s condition, weight, and overall health. Healthcare professionals follow local guidelines and adjust the regimen as needed; patients should not alter the dose without medical advice.

The safety of nimodipine in pregnancy and lactation has not been fully established. It is generally classified as contraindicated or used only when the potential benefit outweighs the risk. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss alternatives with their healthcare provider.

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 (including any special handling) and the necessary import documentation.

Nimotop (nimodipine) is the only calcium‑channel blocker specifically approved for preventing vasospasm after subarachnoid hemorrhage. Other agents, such as hypertensive therapy or endovascular interventions, address vasospasm through different mechanisms. Nimodipine’s advantage lies in its oral administration and targeted cerebral vasodilation, though clinical decisions depend on individual patient factors.

Nimotop tablets should be stored at ambient temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the medication out of reach of children and avoid storing in bathrooms or other humid environments.

Nimotop is taken orally as a tablet, usually with a glass of water. The tablet should be swallowed whole and not crushed or chewed unless specifically instructed by a healthcare professional. Administration timing follows the schedule prescribed by the treating physician.

The most serious risks include severe hypotension, which can lead to dizziness, fainting, or shock, and rare cardiac events such as myocardial ischemia. Hepatic dysfunction and severe allergic reactions are also possible. Patients should be monitored closely for any signs of these complications.

Nimotop should be avoided in patients with known hypersensitivity to nimodipine or any component of the tablet, in those with severe liver impairment, and in individuals taking strong CYP3A4 inhibitors that could raise drug levels. It is also contraindicated in patients with uncontrolled hypotension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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