Fenoldopam Mesylate Baxter
Fenoldopam Mesylate Baxter Uses, Dosage, Side Effects, Food Interaction and all others data.
A dopamine D1 receptor agonist that is used as an antihypertensive agent. It lowers blood pressure through arteriolar vasodilation.
Fenoldopam Mesylate Baxter is an agonist at D1-like dopamine receptors, binds to α2-adrenoceptors, increasing renal blood flow.
Trade Name | Fenoldopam Mesylate Baxter |
Availability | Prescription only |
Generic | Fenoldopam |
Fenoldopam Other Names | Fénoldopam, Fenoldopam, Fenoldopamum |
Related Drugs | hydralazine, nifedipine, captopril, enalapril, labetalol, methyldopa, Corlopam |
Type | |
Formula | C16H16ClNO3 |
Weight | Average: 305.756 Monoisotopic: 305.08187109 |
Groups | Approved |
Therapeutic Class | |
Manufacturer | |
Available Country | USA |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Fenoldopam Mesylate Baxter is a dopamine D1 receptor agonist used for the short term management of hypertension.
For the in-hospital, short-term (up to 48 hours) management of severe hypertension when rapid, but quickly reversible, emergency reduction of blood pressure is clinically indicated, including malignant hypertension with deteriorating end-organ function.
Fenoldopam Mesylate Baxter is also used to associated treatment for these conditions: Malignant Hypertension, Severe Hypertension
How Fenoldopam Mesylate Baxter works
Fenoldopam Mesylate Baxter is a rapid-acting vasodilator. It is an agonist for D1-like dopamine receptors and binds with moderate affinity to α2-adrenoceptors. It has no significant affinity for D2-like receptors, α1 and β-adrenoceptors, 5HT1 and 5HT2 receptors, or muscarinic receptors. Fenoldopam Mesylate Baxter is a racemic mixture with the R-isomer responsible for the biological activity. The R-isomer has approximately 250-fold higher affinity for D1-like receptors than does the S-isomer. In non-clinical studies, fenoldopam had no agonist effect on presynaptic D2-like dopamine receptors, or α or β -adrenoceptors, nor did it affect angiotensin-converting enzyme activity. Fenoldopam Mesylate Baxter may increase norepinephrine plasma concentration.
Toxicity
The most likely reaction of overdose would be excessive hypotension which should be treated with drug discontinuation and appropriate supportive measures.
Food Interaction
- Take on an empty stomach. Orally administered fenoldopam should be taken in a fasted state for optimal absorption.
Fenoldopam Mesylate Baxter Alcohol interaction
[Moderate]
Many psychotherapeutic and CNS-active agents (e.g., anxiolytics, sedatives, hypnotics, antidepressants, antipsychotics, opioids, alcohol, muscle relaxants) exhibit hypotensive effects, especially during initiation of therapy and dose escalation.
Coadministration with antihypertensives and other hypotensive agents, in particular vasodilators and alpha-blockers, may result in additive effects on blood pressure and orthostasis.
Caution and close monitoring for development of hypotension is advised during coadministration of these agents.
Some authorities recommend avoiding alcohol in patients receiving vasodilating antihypertensive drugs.
Patients should be advised to avoid rising abruptly from a sitting or recumbent position and to notify their physician if they experience dizziness, lightheadedness, syncope, orthostasis, or tachycardia.
Fenoldopam Mesylate Baxter Drug Interaction
Moderate: diltiazem, diltiazem, losartan, losartanUnknown: amoxicillin / clavulanate, amoxicillin / clavulanate, sulfamethoxazole / trimethoprim, sulfamethoxazole / trimethoprim, cyclophosphamide, cyclophosphamide, meperidine, meperidine, glucose, glucose, fentanyl, fentanyl, heparin, heparin, sodium iodide, sodium iodide
Fenoldopam Mesylate Baxter Disease Interaction
Major: congestive heart failure, glaucoma, hypokalemia, hypotension, tachycardia
Half Life
The elimination half-life is about 5 minutes in mild to moderate hypertensives, with little difference between the R (active) and S isomers.
Elimination Route
Radiolabeled studies show that about 90% of infused fenoldopam is eliminated in urine, 10% in feces. Elimination is largely by conjugation, without participation of cytochrome P-450 enzymes. Only 4% of the administered dose is excreted unchanged.
Innovators Monograph
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