Gantrisona en es it fr

Gantrisona Brand names, Gantrisona Analogs

Gantrisona Brand Names Mixture

  • Pediazole (Erythromycin (Erythromycin Ethylsuccinate) + Sulfisoxazole Acetyl)
  • Renazone Plus Tab (Ammonium Chloride + Atropine Sulfate + Hyoscyamine Hydrobromide + Scopolamine Hydrobromide + Sulfisoxazole)

Gantrisona Chemical_Formula

C11H13N3O3S

Gantrisona RX_link

No information avaliable

Gantrisona fda sheet

Gantrisona msds (material safety sheet)

Gantrisona MSDS

Gantrisona Synthesis Reference

H. M. Wuest, M. Hoffer, U.S. pat. 2,430,094 (1947 to Hoffmann-La Roche)

Gantrisona Molecular Weight

267.305 g/mol

Gantrisona Melting Point

194 oC

Gantrisona H2O Solubility

0.13 mg/ml (25 oC)

Gantrisona State

Solid

Gantrisona LogP

2.569

Gantrisona Dosage Forms

Tablet; Oral suspension; Eye drops

Gantrisona Indication

Treatment of severe, repeated, or long-lasting urinary tract infections, meningococcal meningitis, acute otitis media, trachoma, inclusion conjunctivitis, nocardiosis, chancroid, toxoplasmosis, malaria and other bacterial infections.

Gantrisona Pharmacology

Sulfisoxazole is a sulfonamide antibiotic. The sulfonamides are synthetic bacteriostatic antibiotics with a wide spectrum against most gram-positive and many gram-negative organisms. However, many strains of an individual species may be resistant. Sulfonamides inhibit multiplication of bacteria by acting as competitive inhibitors of p-aminobenzoic acid in the folic acid metabolism cycle. Bacterial sensitivity is the same for the various sulfonamides, and resistance to one sulfonamide indicates resistance to all. Most sulfonamides are readily absorbed orally. However, parenteral administration is difficult, since the soluble sulfonamide salts are highly alkaline and irritating to the tissues. The sulfonamides are widely distributed throughout all tissues. High levels are achieved in pleural, peritoneal, synovial, and ocular fluids. Although these drugs are no longer used to treat meningitis, CSF levels are high in meningeal infections. Their antibacterial action is inhibited by pus.

Gantrisona Absorption

No information avaliable

Gantrisona side effects and Toxicity

LD50=6800 mg/kg (Orally in mice)

Gantrisona Patient Information

Gantrisona Organisms Affected

Enteric bacteria and other eubacteria