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