D-Dopamine is used to treat low blood pressure due to various causes like heart attack, infection, or surgery. It improves blood flow and urine output, often used under close medical supervision.
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Brief Description of Dopamine Hydrochloride
Consuming alcohol with D-dopamine is unsafe.
Use of D-dopamine during pregnancy may pose risks to the developing baby. Consult your doctor to weigh the benefits against potential risks.
Limited data suggests that D-Dopamine is probably safe during breastfeeding. However, consult your doctor before use.
Do not drive or operate any heavy tools or machines if you experience dizziness or difficulty in seeing bright light after receiving D-Dopamine
Limited information is available on the use of D-dopamine in patients with kidney or liver disease. Consult your doctor for guidance.
Limited information is available on the use of D-dopamine in patients with kidney or liver disease. Consult your doctor for guidance.
D-Dopamine acts on receptors in various organs, improving blood flow, oxygen delivery, and urine production.
Adverse reactions include ectopic beats, nausea, vomiting, tachycardia, anginal pain, palpitations, dyspnoea, headache, hypotension, hypertension, vasoconstriction, and others.
D-Dopamine is recommended for the correction of hemodynamic imbalance present in:
Dopamine is a preparation of Dopamine hydrochloride that stimulates α, β, and dopamine receptors. It is a natural catecholamine formed by the decarboxylation of 3,4-dihydroxyphenylalanine (DOPA). Dopamine produces positive chronotropic and inotropic effects on the myocardium, increasing heart rate and cardiac contractility by exerting an agonist action on β-adrenoceptors and causing the release of norepinephrine from sympathetic nerve endings. Dopamine does not cross the blood-brain barrier and does not activate dopamine receptors in the brain.
Adult dose: Begin infusion at a dosage of 2 to 5 micrograms/kg/min in patients likely to respond to modest increments of heart force and renal perfusion. Increase gradually up to 20 to 50 micrograms/kg/min in seriously ill patients. In patients with severe, refractory, chronic congestive heart failure, doses should be started at 0.5 to 2 micrograms/kg/min and increased as urinary output increases.
Children less than 12 years old: Safety and efficacy have not been established.
Geriatric patients: No variation in dosage is suggested, but close monitoring is required.
D-dopamine must be diluted before administration to patients using sterile intravenous solutions. Dilutions should be made just before administration.
The action of D-D-Dopamine is potentiated by monoamine oxidase inhibitors (MAOIs). Concurrent administration of cyclopropane or halogenated hydrocarbon anesthetics may cause ventricular arrhythmias. β-adrenergic blocking agents antagonize the cardiac effects of D-D-Dopamine.
Dopamine hydrochloride is contraindicated in patients with known hypersensitivity to dopamine, phaeochromocytoma, uncorrected tachyarrhythmias, or ventricular fibrillation.
The drug may be used in pregnant women when the expected benefits outweigh the potential risks to the fetus. Use in breastfeeding mothers is not recommended unless the benefits outweigh the risks.
Administer cautiously in patients with impaired renal and hepatic function, and closely monitor blood pressure, urine flow, and tissue perfusion. Correct hypovolaemia before treatment with D-D-Dopamine. Avoid extravasation, and use with caution in patients inhaling cyclopropane or halogenated hydrocarbon anesthetics.
Store below 25°C and protect from light. Diluted solutions are stable for a minimum of 24 hours when stored as recommended. Avoid mixing with alkaline intravenous solutions or amphotericin B solution.
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