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## Overview
Nimodipine is a calcium channel blocker with a higher affinity for cerebral arteries compared to peripheral arteries. It is primarily used to prevent cerebral vasospasm following subarachnoid hemorrhage (SAH).
## Primary Indications
* Prevention of cerebral vasospasm and subsequent ischemic neurologic deficits in patients who have experienced a subarachnoid hemorrhage (SAH).
## Adult Dosing
* **Oral:** 60 mg every 4 hours for 21 days.
* Dosing may begin as soon as possible, preferably within 72 hours of SAH.
* If oral administration is not feasible, a nasogastric tube may be used. The capsules should be pierced and the contents administered via NG tube. Do not administer the capsule contents directly into the NG tube without dilution.
* **Intravenous (IV) administration of oral nimodipine solution is NOT recommended due to risk of fatal overdose. Specifically formulated IV nimodipine is available in some regions but is not widely available.**
## Pediatric Dosing
* Pediatric dosing for nimodipine is not established. Use in pediatric patients is generally not recommended.
## Dose Adjustments
* No specific dose adjustments are routinely recommended for hepatic or renal impairment. However, caution and close monitoring are advised, particularly in patients with severe hepatic dysfunction, as metabolism may be reduced.
## Contraindications
* Hypersensitivity to nimodipine or any component of the formulation.
* Concurrent use with strong CYP3A4 inhibitors (e.g., ritonavir).
## Adverse Effects
* **Common:** Hypotension, headache, nausea, gastrointestinal upset.
* **Less Common:** Dizziness, flushing, edema, rash, elevated liver enzymes.
* **Serious:** Severe hypotension, myocardial infarction, heart failure.
## Key Drug Interactions
* **CYP3A4 Inhibitors:** Concurrent use with strong CYP3A4 inhibitors (e.g., ritonavir, ketoconazole, itraconazole, grapefruit juice) can significantly increase nimodipine plasma concentrations, leading to potential toxicity. Avoid coadministration.
* **CYP3A4 Inducers:** Concurrent use with CYP3A4 inducers (e.g., rifampin, carbamazepine, phenytoin, phenobarbital) can decrease nimodipine plasma concentrations, potentially reducing efficacy.
* **Antihypertensives:** Additive hypotensive effects may occur when used concurrently with other antihypertensive agents.
## Monitoring
* **Blood Pressure:** Monitor blood pressure regularly, especially during initiation of therapy and dose adjustments, and particularly if administered concurrently with other antihypertensives.
* **Neurological Status:** Assess neurological status for any signs of recurrent vasospasm or neurological deficit.
* **Liver Function Tests:** Monitor liver function periodically, especially in patients with pre-existing liver disease.
## Clinical Pearls
* Nimodipine's efficacy is primarily in preventing the *consequences* of vasospasm, not in directly reversing existing vasospasm.
* The oral formulation is the standard of care for SAH outside of specific IV formulations.
* Careful administration is crucial for the oral suspension via NG tube to avoid overdose.
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**Disclaimer:** This information is intended for clinical use and does not substitute for professional medical advice. Always consult the most current prescribing information and institutional protocols before making any treatment decisions.