Details of Drug-Drug Interaction
| Drug General Information (ID: DDI8R1UM5S) | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Nimodipine | Drug Info | Rapacuronium | Drug Info | |||||
| Drug Type | Small molecule | Small molecule | |||||||
| Therapeutic Class | Vasodilator Agents | Neuromuscular Blocking Agents | |||||||
| Structure | |||||||||
| Mechanism of Nimodipine-Rapacuronium Interaction (Severity Level: Moderate) | |||||||||
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| Additive neuromuscular blocking effects Click to Show/Hide Mechanism Graph | |||||||||
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| Drug Name | Nimodipine | Rapacuronium | |||||||
| Mechanism | Potentiates neuromuscular blockade |
Neuromuscular blocking agent Neuronal acetylcholine receptor Antagonist |
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| Key Mechanism Factor 1 | |||||||||
| Factor Name | Neuronal acetylcholine receptor | Structure Sequence | |||||||
| Protein Family | Ligand-gated ion channel (TC 1.A.9) family | ||||||||
| Protein Function |
After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane.
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| Mechanism Description |
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| Recommended Action | |||||||||
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| Management | Patients should be closely monitored for prolonged neuromuscular blockade. Reduced doses of muscle relaxants may be necessary. Profound neuromuscular blockade may be reversed by neostigmine or edrophonium. | ||||||||

