Cremodiazine
Cremodiazine Brand names, Cremodiazine 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
Cremodiazine Brand Names Mixture
- No information avaliable
Cremodiazine Chemical_Formula
C10H10N4O2S
Cremodiazine RX_link
http://www.rxlist.com/cgi/generic3/silversulf.htm
Cremodiazine fda sheet
Cremodiazine msds (material safety sheet)
Cremodiazine Synthesis Reference
No information avaliable
Cremodiazine Molecular Weight
250.278 g/mol
Cremodiazine Melting Point
No information avaliable
Cremodiazine H2O Solubility
No information avaliable
Cremodiazine State
Solid
Cremodiazine LogP
1.883
Cremodiazine Dosage Forms
Cream
Cremodiazine Indication
For the treatment of rheumatic fever and meningococcal meningitis
Cremodiazine 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.
Cremodiazine Absorption
No information avaliable
Cremodiazine side effects and Toxicity
No information avaliable
Cremodiazine Patient Information
No information avaliable
Cremodiazine Organisms Affected
Enteric bacteria and other eubacteria
