Terfonyl
Terfonyl Brand names, Terfonyl Analogs
- Adiazin
- Adiazine
- Coco-Diazine
- Cocodiazine
- Codiazine
- Cremodiazine
- Cremotres
- Debenal
- Deltazina
- Diazin
- Diazolone
- Diazovit
- Diazyl
- Eskadiazine
- Honey Diazine
- Lantrisul
- Lipo-Diazine
- Lipo-Levazine
- Liquadiazine
- Metha-Meridiazine
- Microsulfon
- Neazine
- Neotrizine
- Palatrize
- Pecta-Diazine, Suspension
- Piridisir
- Pirimal
- Pyrimal
- Quadetts
- Quadramoid
- SDA
- Sanodiazine
- Sildaflo
- Silvadene
- Spofadrizine
- Ssd
- Sterazine
- Sulfa-Triple #2
- Sulfacombin
- Sulfadiazene
- Sulfadiazin
- Sulfaloid
- Sulfanilamidopyrimidine
- Sulfapirimidin
- Sulfapyrimidin
- Sulfapyrimidine
- Sulfatryl
- Sulfazin
- Sulfazine
- Sulfolex
- Sulfonamides Duplex
- Sulfonsol
- Sulfose
- Sulphadiazine
- Terfonyl
- Theradiazine
- Thermazene
- Tri-Sulfameth
- Trifonamide
- Triple Sulfa
- Triple Sulfas
- Triple Sulfoid
- Trisem
- Trisulfapyrimidine, Oral Suspension
- Truozine
Terfonyl Brand Names Mixture
- No information avaliable
Terfonyl Chemical_Formula
C10H10N4O2S
Terfonyl RX_link
http://www.rxlist.com/cgi/generic3/silversulf.htm
Terfonyl fda sheet
Terfonyl msds (material safety sheet)
Terfonyl Synthesis Reference
No information avaliable
Terfonyl Molecular Weight
250.278 g/mol
Terfonyl Melting Point
No information avaliable
Terfonyl H2O Solubility
No information avaliable
Terfonyl State
Solid
Terfonyl LogP
1.883
Terfonyl Dosage Forms
Cream
Terfonyl Indication
For the treatment of rheumatic fever and meningococcal meningitis
Terfonyl Pharmacology
Sulfadiazine 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.
Terfonyl Absorption
No information avaliable
Terfonyl side effects and Toxicity
No information avaliable
Terfonyl Patient Information
No information avaliable
Terfonyl Organisms Affected
Enteric bacteria and other eubacteria
