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