GNH USA

Europe — EMA

Nimodipino Stadafarma (Nimodipine)

GNH USA supplies Nimodipino Stadafarma (Nimodipine), a calcium channel blocker to prevent cerebral vasospasm after hemorrhage. Request a quote for supply.

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What is Nimodipine?

Nimodipine, the active ingredient in Nimodipino Stadafarma, is a calcium channel blocker of the dihydropyridine class presented as an oral tablet for oral administration. It works by selectively antagonising L‑type calcium channels in cerebral vessels, thereby reducing the risk of vasospasm after subarachnoid hemorrhage in adult patients.

GNH USA supplies Nimodipino Stadafarma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality and regulatory conformity across markets.

What is Nimodipine used for?

Nimodipine acts on cerebral vasculature to prevent vasospasm following subarachnoid hemorrhage.

- Subarachnoid hemorrhage: reduces the incidence and severity of cerebral vasospasm after aneurysmal bleed.

What are the side effects of Nimodipine?

Nimodipine may cause a range of adverse reactions, from mild to severe.

Common Side Effects: - Headache: mild to moderate pain often reported during therapy. - Dizziness: sensation of light‑headedness, especially when standing quickly. - Hypotension: reduction in blood pressure, may cause faintness. - Nausea: upset stomach or urge to vomit. - Flushing: warm, reddened skin, usually on the face or neck. - Constipation: reduced bowel movements.

Serious or Rare Side Effects: - Severe hypotension: marked drop in blood pressure requiring medical attention. - Bradycardia: unusually slow heart rate that may be symptomatic. - Hepatic dysfunction: abnormal liver enzyme elevations. - Allergic reaction: rash, itching, swelling, or anaphylaxis. - Stevens‑Johnson syndrome: severe skin and mucous membrane disorder. - Seizures: rare neurologic events requiring urgent care.

What precautions apply to Nimodipine?

Before initiating Nimodipino Stadafarma, clinicians should consider several safety measures.

- Blood pressure monitoring: check systolic and diastolic values regularly during therapy. - CYP3A4 inhibitors: avoid concomitant use with strong inhibitors to prevent excess drug exposure. - Hepatic impairment: use with caution in patients with liver dysfunction, adjusting dose if necessary. - Pregnancy and lactation: assess risk‑benefit ratio before prescribing to pregnant or nursing women. - Hypersensitivity: discontinue immediately if signs of allergic reaction appear. - Store at ambient temperature below 25°C: keep in the original container, protect from moisture and light.

What does Nimodipine interact with?

Nimodipine can interact with several medicines, influencing its safety and effectiveness.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise plasma levels and increase toxicity. - Concurrent potent vasodilators (e.g., nitroglycerin): additive hypotensive effect can be dangerous. - Grapefruit juice: can elevate nimodipine concentrations, heightening adverse effects.

Moderate Interactions (Monitor Closely): - Other antihypertensives (beta‑blockers, ACE inhibitors): monitor blood pressure for excessive lowering. - Diuretics: watch electrolytes and blood pressure for synergistic effects. - Antiepileptic drugs (phenytoin, carbamazepine): may reduce nimodipine levels, requiring efficacy assessment.

Frequently asked questions

What is Nimodipino Stadafarma used for?+
Nimodipino Stadafarma contains nimodipine, which is prescribed to prevent cerebral vasospasm in patients who have suffered a subarachnoid hemorrhage. By improving blood flow in the brain’s arteries, it helps reduce the risk of delayed ischemic neurological deficits that can follow the bleed.
How does nimodipine work in the body?+
Nimodipine selectively blocks L‑type calcium channels on the smooth muscle of cerebral arteries. This blockade reduces calcium entry into the cells, causing the vessels to relax and dilate. The resulting vasodilation improves cerebral perfusion and lessens the likelihood of vasospasm after a hemorrhagic event.
What is the usual dose of Nimodipino Stadafarma?+
The appropriate dose of Nimodipino Stadafarma is determined by the prescribing clinician based on the patient’s condition, age, weight, and renal or hepatic function. Dosage regimens are individualized and should follow the prescribing information provided by the healthcare professional.
Is Nimodipino Stadafarma safe during pregnancy or breastfeeding?+
Safety data for nimodipine in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any possible risk to the fetus or infant. Healthcare providers must evaluate the risk‑benefit profile before prescribing to pregnant or nursing women.
How do I order Nimodipino Stadafarma from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA 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.
How does Nimodipino Stadafarma compare with other vasospasm treatments?+
Nimodipine is the only calcium‑channel blocker specifically approved for preventing cerebral vasospasm after subarachnoid hemorrhage. Other agents, such as clazosentan or endothelin‑receptor antagonists, target different pathways and have distinct safety profiles. Nimodipine’s oral route and well‑characterised pharmacology make it a first‑line option in many guidelines.
What are the recommended storage conditions for Nimodipino Stadafarma?+
Store Nimodipino Stadafarma at ambient temperature below 25 °C. Keep the tablets in their original packaging, protect them from moisture, heat and direct sunlight. Do not refrigerate or freeze the product, as temperature extremes can affect tablet integrity.
How is Nimodipino Stadafarma administered?+
Nimodipino Stadafarma is taken orally, usually with a glass of water. The tablet should be swallowed whole and not crushed or chewed unless otherwise directed by a healthcare professional. Administration timing (e.g., with or without food) follows the prescriber’s instructions.
What are the most serious risks associated with Nimodipino Stadafarma?+
The most serious risks include severe hypotension, bradycardia, and rare but potentially life‑threatening allergic reactions such as anaphylaxis or Stevens‑Johnson syndrome. Patients should be monitored for sudden drops in blood pressure, slow heart rate, or any signs of hypersensitivity, and medical attention should be sought immediately if they occur.
Who should not use Nimodipino Stadafarma?+
Nimodipino Stadafarma should be avoided in individuals with known hypersensitivity to nimodipine or any component of the formulation. Caution is also advised for patients with severe hepatic impairment, uncontrolled hypotension, or those taking contraindicated strong CYP3A4 inhibitors. The prescriber decides suitability on a case‑by‑case basis.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Nimodipine
Route
Oral Use
Manufacturer
Laboratorio Stada, S.L.
Origin
EU

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