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Mazicon Brand names, Mazicon Analogs

Mazicon Brand Names Mixture

  • No information avaliable

Mazicon Chemical_Formula

C32H26N4O2

Mazicon RX_link

No information avaliable

Mazicon fda sheet

Mazicon FDA

Mazicon msds (material safety sheet)

Mazicon Synthesis Reference

No information avaliable

Mazicon Molecular Weight

498.575 g/mol

Mazicon Melting Point

No information avaliable

Mazicon H2O Solubility

Very slightly soluble (0.15 mg/mL at 23oC)

Mazicon State

Solid

Mazicon LogP

5.955

Mazicon Dosage Forms

Liquid (ampule containing 20 mg conivaptan hydrochloride)

Mazicon Indication

For the treatment of euvolemic hyponatremia (e.g. the syndrome of inappropriate secretion of antidiuretic hormone, or in the setting of hypothyroidism, adrenal insufficiency, pulmonary disorders, etc.) in hospitalized patients.

Mazicon Pharmacology

Conivaptan is a nonpeptide, dual antagonist of arginine vasopressin (AVP) V1A and V2 receptors. The level of AVP in circulating blood is critical for the regulation of water and electrolyte balance and is usually elevated in both euvolemic and hypervolemic hyponatremia. The AVP effect is mediated through V2 receptors, which are functionally coupled to aquaporin channels in the apical membrane of the collecting ducts of the kidney. These receptors help to maintain plasma osmolality within the normal range. The predominant pharmacodynamic effect of conivaptan in the treatment of hyponatremia is through its V2 antagonism of AVP in the renal collecting ducts, an effect that results in aquaresis, or excretion of free water. The pharmacodynamic effects of conivaptan include increased free water excretion (i.e., effective water clearance [EWC]) generally accompanied by increased net fluid loss, increased urine output, and decreased urine osmolality.

Mazicon Absorption

No information avaliable

Mazicon side effects and Toxicity

Although no data on overdosage in humans are available, conivaptan has been administered as a 20 mg loading dose on Day 1 followed by continuous infusion of 80 mg/day for 4 days in hyponatremia patients and up to 120 mg/day for 2 days in CHF patients. No new toxicities were identified at these higher doses, but adverse events related to the pharmacologic activity of conivaptan, e.g. hypotension and thirst, occurred more frequently at these higher doses.

Mazicon Patient Information

No information avaliable

Mazicon Organisms Affected

Humans and other mammals