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Pronunciation |
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(NIL
va di
peen) |

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Synonyms |
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Nivadipine |

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Pharmacological Index |
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Calcium Channel Blocker |

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Contraindications |
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Acute apoplectic stroke; intracranial hemorrhage; raised intracranial
pressure |

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Adverse
Reactions |
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Cardiovascular: Flushing, tachycardia, edema, hypotension, ectopy
(ventricular), shock, chest pain, angina, palpitations, sinus tachycardia,
arrhythmias (ventricular)
Central nervous system: Headache, dizziness, sleep disturbances, insomnia
Gastrointestinal: Nausea
Ocular: Oscillopsia |

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Mechanism of
Action |
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Dihydropyridine calcium channel blocking agent with properties similar to
nifedipine |

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Pharmacodynamics/Kinetics |
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Protein binding: 98%
Distribution: Vd: 24-40 L/kg
Bioavailability: Oral: 14% to 19%
Half-life: 9.8-18.2 hours
Elimination: Renal; clearance: 1.08 L/kg/hour |

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Usual Dosage |
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Hypertension: 4-16 mg/day; reduce dosage to a maximum dose of 8 mg in
patients with cirrhosis or with concomitant use with cimetidine
Cerebrovascular disease: 2-4 mg twice daily
Angina pectoris: 8-16 mg/day |

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Cardiovascular
Considerations |
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Nilvadipine alone or in combination with other agents may be used in the
management of hypertension and angina. Nilvadipine should be avoided in patients
with left ventricular systolic dysfunction because of negative inotropic
effects. |

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