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