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 an oral tablet for systemic use. It is indicated for the prophylaxis of cerebral vasospasm in patients who have suffered a subarachnoid hemorrhage, helping to preserve cerebral blood flow.

GNH India supplies Nimotop as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company follows stringent quality standards to provide reliable sourcing across multiple regions for global healthcare providers and ensure compliance with regulatory requirements.

Manufacturer / TM Owner

Laboratoire Xo

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Indications & Clinical Uses

Nimotop (nimodipine) is used in the management of cerebrovascular conditions, specifically to prevent vasospasm after bleeding in the brain.

  • Cerebral vasospasm after subarachnoid hemorrhage: reduces narrowing of cerebral arteries and helps maintain adequate cerebral perfusion.
  • Delayed cerebral ischemia following aneurysmal SAH: lowers the incidence of secondary ischemic neurological deficits.
  • Neuroprotective support in acute brain injury: may improve cerebral blood flow and oxygen delivery during the early recovery phase.

How It Works

  • Nimodipine antagonizes L‑type voltage‑gated calcium channels on vascular smooth muscle, especially in cerebral arteries. By inhibiting calcium influx, it induces selective vasodilation of intracranial vessels, increasing cerebral blood flow without markedly affecting systemic blood pressure, providing a clinically favorable profile. The drug crosses the blood‑brain barrier, allowing direct action on cerebral vasculature, which contributes to its efficacy in preventing vasospasm after subarachnoid hemorrhage.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate pain often reported during therapy.
  • Hypotension: transient lowering of blood pressure, especially when standing.
  • Nausea: occasional stomach upset or queasiness.
  • Flushing: warm sensation and reddening of the skin.
  • Dizziness: feeling light‑headed or unsteady.
  • Constipation: reduced bowel movements.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Bradycardia: abnormally slow heart rate that may need intervention.
  • Allergic reaction: rash, itching, swelling, or anaphylaxis.
  • Liver enzyme elevation: increased transaminases indicating hepatic stress.
  • Myocardial infarction: rare occurrence of heart attack.
  • Thrombocytopenia: low platelet count leading to bleeding risk.

Precautions & Warnings

Before prescribing Nimotop, clinicians should consider several precautionary measures to ensure safe use.

  • Renal impairment: monitor renal function and adjust therapy as needed.
  • Hepatic impairment: use with caution; assess liver enzymes regularly.
  • Concomitant antihypertensives: risk of additive blood‑pressure lowering effects.
  • Elderly patients: increased sensitivity to hypotension; start at lower dose if applicable.
  • Pregnancy: safety not established; avoid unless benefit outweighs risk.
  • Store at ambient temperature: keep below 25 °C in the original packaging, protect from moisture.

Avoid Interactions

Nimotop can interact with other medicines, altering its effectiveness or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., clarithromycin, itraconazole): may increase plasma concentrations.
  • Other calcium channel blockers: additive vasodilatory and hypotensive effects.
  • Grapefruit juice: can raise drug levels and risk of adverse events.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: monitor heart rate and blood pressure for excessive slowing.
  • Diuretics: watch for enhanced hypotensive response.
  • Antihypertensive agents: dose adjustments may be required to avoid over‑lowering blood pressure.

Frequently Asked Questions

Nimotop contains nimodipine, a calcium channel blocker that is specifically indicated to prevent cerebral vasospasm after a subarachnoid hemorrhage. By maintaining the diameter of cerebral arteries, it helps reduce the risk of delayed ischemic neurological deficits in patients who have experienced bleeding in the brain.

Nimodipine blocks L‑type voltage‑gated calcium channels on the smooth muscle of cerebral blood vessels. This inhibition reduces calcium entry, causing selective dilation of intracranial arteries, which improves cerebral blood flow while having limited impact on systemic blood pressure.

The exact dose of Nimotop is determined by the prescribing clinician based on the patient’s clinical condition, weight, renal and hepatic function, and response to therapy. Dosage regimens are individualized and should follow the prescriber’s instructions and local guidelines.

Safety data for nimodipine in pregnancy and lactation are limited. The product is classified as having an unknown pregnancy category, so it should only be used when the potential benefit justifies the potential risk to the fetus. Breastfeeding mothers should consult their healthcare provider before use.

To order 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 high lipophilicity, which allows it to cross the blood‑brain barrier and preferentially dilate cerebral vessels. Other calcium channel blockers, such as amlodipine, are less selective for intracranial arteries and are not approved for preventing vasospasm after subarachnoid hemorrhage.

Nimotop tablets should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original blister pack, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Nimotop is taken orally as a tablet. The tablet should be swallowed whole with water and can be taken with or without food, unless the prescribing physician provides specific instructions regarding timing relative to meals.

Serious risks include severe hypotension, bradycardia, allergic reactions such as rash or anaphylaxis, significant liver enzyme elevations, myocardial infarction, and thrombocytopenia. Patients should seek immediate medical attention if they experience symptoms like faintness, rapid heartbeat, chest pain, severe skin reactions, or unusual bleeding.

Nimotop should be avoided in patients with known hypersensitivity to nimodipine or any excipients in the tablet. Caution is advised for individuals with severe hepatic impairment, uncontrolled hypotension, or those taking contraindicated strong CYP3A4 inhibitors. Pregnant women should only use it when clearly indicated by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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