Clevidipine Iv

Drug Overview

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drug details
nameClevidipine
route of administrationIV
classificationCalcium channel blocker, vasodilator
pharmacokinetics
absorptionRapidly absorbed after IV administration; reaches peak plasma concentration within minutes
distributionDistributes extensively to tissues; highly protein-bound
metabolismMetabolized primarily by the liver; undergoes ester hydrolysis
excretionEliminated primarily as inactive metabolites in the urine and bile
suggested dosage
generalDosage should be individualized based on patient response and blood pressure goals. Initiation and titration are critical.
starting dose1-2 mcg/kg/min IV
titrationTitrate dose up or down every 2-5 minutes in increments of 0.5-2 mcg/kg/min, to achieve the desired blood pressure.
maximum dose20 mcg/kg/min
patient specific considerationsAdjusting for factors such as age, renal function, or concomitant medications is important for accurate and safe dosage calculation.
weight specific considerationsThe suggested initial dosage range is tailored for a 70 kg individual.
indicationsHypertension crisis, particularly in acute situations like acute aortic dissection, post-operative hypertension, and during cardiac procedures.
safety in pregnancy
classificationCategory C
explanationAnimal studies have shown adverse effects, but adequate and well-controlled studies in pregnant women are lacking. Use only if potential benefits outweigh risks.
safety in breastfeeding
classificationNot established
explanationLimited data are available about clevidipine excretion into breast milk. Breastfeeding is not recommended during treatment.
side effects
1Headache
2Hypotension
3Nausea
4Vomiting
5Flushing
6Dizziness
7Tachycardia
8Arrhythmias (less common)
9Rash (less common)
10Palpitations
11Fever (less common)
alternatives
1Nicardipine
2Nitroprusside
3Nitroglycerin
4Esmolol
contraindications
1Severe hypotension
2Hypersensitivity to clevidipine or any of its components
3Severe bradycardia
interactions
other medicationsInhibitors of hepatic drug-metabolizing enzymes, particularly those with a similar mechanism of action may modify clevidipine's effect. Consult with pharmacist or physician on the potential for drug-drug interaction.
foodsNo significant known food interactions with clevidipine.
warnings and precautions
1Closely monitor blood pressure and heart rate during and after administration
2Rapid reductions in blood pressure can be dangerous. Adjust the dose carefully and avoid over-titration.
3Monitor for signs of bradycardia, hypotension, and cardiac dysfunction.
4Potential for allergic reactions (including angioedema and anaphylaxis)
5Infusion-related reactions (e.g., fever, chills, flushing, urticaria) can occur
6Risk of lipid-related adverse reactions (e.g., hypertriglyceridemia and pancreatitis in rare cases) due to the emulsion formulation.
7Caution in patients with severe liver or renal disease
additional information
special instructionsInfusion should be administered via dedicated IV line. Avoid use in patients with severe lipid disorders or those at high risk.
monitoring recommendationsContinuous cardiac monitoring and frequent blood pressure measurements are crucial during clevidipine infusion.
patient specific informationAge and weight considerations are used to calculate the appropriate dosage range. The provided starting dose and titration recommendations are guidelines and should be tailored based on patient response and physician judgment. A comprehensive patient history including past medical conditions, allergies, and medications currently being taken is important for appropriate clinical management.
disclaimerThis information is for educational purposes only and does not constitute medical advice. Always consult with a qualified healthcare professional before starting or stopping any medication.

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Reference Patient:(25 years,Male, 70KGs) *Not a medical advice

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