Chloromycetin Hydrocortisone

Chloromycetin Hydrocortisone Brand names, Chloromycetin Hydrocortisone Analogs

Chloromycetin Hydrocortisone Brand Names Mixture

No information avaliable

Chloromycetin Hydrocortisone Chemical_Formula

C₁₁H₁₂Cl₂N₂O₅

Chloromycetin Hydrocortisone RX_link

http://www.rxlist.com/cgi/generic3/chloramphenicol.htm

Chloromycetin Hydrocortisone fda sheet

Chloromycetin_Hydrocortisone FDA

Chloromycetin Hydrocortisone msds (material safety sheet)

Chloromycetin_Hydrocortisone MSDS

Chloromycetin Hydrocortisone Synthesis Reference

No information avaliable

Chloromycetin Hydrocortisone Molecular Weight

323.129 g/mol

Chloromycetin Hydrocortisone Melting Point

150.5 ^oC

Chloromycetin Hydrocortisone H₂O Solubility

2500 mg/L (at 25 °C)

Chloromycetin Hydrocortisone State

Solid

Chloromycetin Hydrocortisone LogP

1.476

Chloromycetin Hydrocortisone Dosage Forms

Capsule; Drops; Liquid; Ointment; Powder; Solution; Suspension; Tablet

Chloromycetin Hydrocortisone Indication

Used in treatment of cholera, as it destroys the vibrios and decreases the diarrhea. It is effective against tetracycline-resistant vibrios. It is also used in eye drops or ointment to treat bacterial conjunctivitis.

Chloromycetin Hydrocortisone Pharmacology

Chloramphenicol is a broad-spectrum antibiotic that was derived from the bacterium Streptomyces venezuelae and is now produced synthetically. Chloramphenicol is effective against a wide variety of microorganisms, but due to serious side-effects (e.g., damage to the bone marrow, including aplastic anemia) in humans, it is usually reserved for the treatment of serious and life-threatening infections (e.g., typhoid fever). Chloramphenicol is bacteriostatic but may be bactericidal in high concentrations or when used against highly susceptible organisms. Chloramphenicol stops bacterial growth by binding to the bacterial ribosome (blocking peptidyl transferase) and inhibiting protein synthesis.

Chloromycetin Hydrocortisone Absorption

Rapidly and completely absorbed from gastrointestinal tract following oral administration (bioavailability 80%). Well absorbed following intramuscular administration (bioavailability 70%). Intraocular and some systemic absorption also occurs after topical application to the eye.

Chloromycetin Hydrocortisone side effects and Toxicity

Oral, mouse: LD₅₀ = 1500 mg/kg; Oral, rat: LD₅₀ = 2500 mg/kg. Toxic reactions including fatalities have occurred in the premature and newborn; the signs and symptoms associated with these reactions have been referred to as the gray syndrome. Symptoms include (in order of appearance) abdominal distension with or without emesis, progressive pallid cyanosis, vasomotor collapse frequently accompanied by irregular respiration, and death within a few hours of onset of these symptoms.

Chloromycetin Hydrocortisone Patient Information