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Presolisin Brand names, Presolisin Analogs

Presolisin Brand Names Mixture

  • No information avaliable

Presolisin Chemical_Formula

C56H71N9O23S

Presolisin RX_link

http://www.rxlist.com/cgi/generic4/mycamine.htm

Presolisin fda sheet

Presolisin FDA

Presolisin msds (material safety sheet)

Presolisin MSDS

Presolisin Synthesis Reference

No information avaliable

Presolisin Molecular Weight

1270.28 g/mol

Presolisin Melting Point

No information avaliable

Presolisin H2O Solubility

Freely soluble as sodium salt (> 200mg/mL)

Presolisin State

Solid

Presolisin LogP

No information avaliable

Presolisin Dosage Forms

Powder for solution (for injection)

Presolisin Indication

For use in the treatment of patients with esophageal candidiasis and prophylaxis of Candida infections in patients undergoing hematopoietic stem cell transplantation.

Presolisin Pharmacology

Formerly known as FK463, micafungin is a novel antifungal agent. It is a glucan synthesis inhibitor of the echinocandin structural class. The U.S. Food and Drug Administration approved micafungin in March 2005. Micafungin inhibits an enzyme essential for fungal cell-wall synthesis and is fungicidal (lethal) for Candida. Micafungin can be used concomitantly with a variety of other drugs, including the HIV protease inhibitor ritonavir and the transplant medications cyclosporine and tacrolimus.

Presolisin Absorption

No information avaliable

Presolisin side effects and Toxicity

Intravenous LD50 in rats is 125mg/kg. In dogs it is >200mg/kg. No cases of overdosage have been reported. Repeated daily doses up to 8 mg/kg (maximum total dose of 896 mg) in adult patients have been administered in clinical trials with no reported dose-limiting toxicity. The minimum lethal dose is 125 mg/kg in rats, equivalent to 8.1 times the recommended human clinical dose for esophageal candidiasis based on body surface area comparisons.

Presolisin Patient Information

No information avaliable

Presolisin Organisms Affected

Aspergillis, Candida and other fungi