G-Mycin

G-Mycin Brand names, G-Mycin Analogs

G-Mycin Brand Names Mixture

Diprogen Crm (Betamethasone Dipropionate + Gentamicin Sulfate)
Diprogen Ont (Betamethasone Dipropionate + Gentamicin Sulfate)
Garasone Oph/Ot Sol (Betamethasone + Gentamicin Sulfate)
Garasone Ophthalmic Ointment (Betamethasone + Gentamicin Sulfate)
Gentamicin Sulfate in Nacl 0.9% Inj (Gentamicin Sulfate + Sodium Chloride)
Gentamicin Sulfate in Nacl 0.9% Inj (Gentamicin Sulfate + Sodium Chloride)
Gentocin Durafilm (Betamethasone 21-Acetate + Gentamicin Sulfate)
Gentocin Otic Solution (Betamethasone + Gentamicin Sulfate)
Otomax Ointment (Betamethasone + Clotrimazole + Gentamicin Sulfate)
Sandoz Pentasone (Betamethasone + Gentamicin Sulfate)
Topagen Ont (Betamethasone + Gentamicin Sulfate)
Topagen Spray (Betamethasone + Gentamicin Sulfate)
Valisone G Cream (Betamethasone + Gentamicin Sulfate)
Valisone G Ointment (Betamethasone + Gentamicin Sulfate)

G-Mycin Chemical_Formula

C₂₁H₄₃N₅O₇

G-Mycin RX_link

http://www.rxlist.com/cgi/generic2/pedgenta.htm

G-Mycin fda sheet

G-Mycin msds (material safety sheet)

G-Mycin MSDS

G-Mycin Synthesis Reference

No information avaliable

G-Mycin Molecular Weight

477.596 g/mol

G-Mycin Melting Point

105°C (218-237°C as sulfate salt)

G-Mycin H₂O Solubility

100 mg/mL

G-Mycin State

Solid

G-Mycin LogP

-3.637

G-Mycin Dosage Forms

Cream; Drops; Liquid; Ointment; Solution

G-Mycin Indication

For treatment of serious infections caused by susceptible strains of the following microorganisms: P. aeruginosa, Proteus species (indole-positive and indole-negative), E. coli, Klebsiella-Enterobactor-Serratia species, Citrobacter species and Staphylococcus species (coagulase-positive and coagulase-negative).

G-Mycin Pharmacology

Gentamicin is a broad spectrum aminoglycoside antibiotic. Aminoglycosides work by binding to the bacterial 30S ribosomal subunit, causing misreading of t-RNA, leaving the bacterium unable to synthesize proteins vital to its growth. Aminoglycosides are useful primarily in infections involving aerobic, Gram-negative bacteria, such as Pseudomonas, Acinetobacter, and Enterobacter. In addition, some mycobacteria, including the bacteria that cause tuberculosis, are susceptible to aminoglycosides. Infections caused by Gram-positive bacteria can also be treated with aminoglycosides, but other types of antibiotics are more potent and less damaging to the host. In the past the aminoglycosides have been used in conjunction with penicillin-related antibiotics in streptococcal infections for their synergistic effects, particularly in endocarditis. Aminoglycosides are mostly ineffective against anaerobic bacteria, fungi and viruses.

G-Mycin Absorption

Injections lead to peak serum concentrations in 30-60 minutes. Topical gentamicin is readily absorbed from large burned, denuded, or granulating areas but not through intact skin. Absorption of gentamicin is faster and greater with the cream compared to the ointment. Gentamicin is absorbed in small quantities following topical application to the eye. Gentamicin is also absorbed in small amounts following topical application to the ear (especially if the eardrum is perforated or if tissue damage is present).

G-Mycin side effects and Toxicity

Mouse, intravenous LD₅₀: 52 mg/kg; rat, intravenous LD₅₀: 96 mg/kg.

G-Mycin Patient Information