Indication |
For the treatment of initial and recurrent urinary tract
infections in adults caused by the following susceptible microorganisms:
Escherichia coli, Proteus mirabilis, Proteus vulgaris, Klebsiella species (including K. pneumoniae), and Enterobacter species. |
Pharmacodynamics |
Cinoxacin is a synthetic antibacterial agent with in vitro
activity against many gram-negative aerobic bacteria, particularly
strains of the Enterobacteriaceae family. Cinoxacin inhibits bacterial
deoxyribonucleic acid (DNA) synthesis, is bactericidal, and is active
over the entire urinary pH range. Cross resistance with nalidixic acid
has been demonstrated. |
Mechanism of action |
Evidence exists that cinoxacin binds strongly, but reversibly, to
DNA, interfering with synthesis of RNA and, consequently, with protein
synthesis. It appears to also inhibit DNA gyrase. This enzyme is
necessary for proper replicated DNA separation. By inhibiting this
enzyme, DNA replication and cell division is inhibited. |
Absorption |
Rapidly absorbed after oral administration. The presence of food delays absorption but does does not affect total absorption. |
Volume of distribution |
Not Available |
Protein binding |
60 to 80% |
Metabolism |
Hepatic, with approximately 30-40% metabolized to inactive metabolites. |
Route of elimination |
Not Available |
Half life |
The mean serum half-life is 1.5 hours. Half-life in patients with impaired renal function may exceed 10 hours. |
Clearance |
Not Available |
Toxicity |
Oral, subcutaneous, and intravenous LD50 in the rat is 3610 mg/kg, 1380 mg/kg, and 860 mg/kg, respectively. Oral, subcutaneous, and intravenous LD50
in the mouse is 2330 mg/kg, 900 mg/kg, and 850 mg/kg,
respectively.Symptoms following an overdose of cinoxacin may include
anorexia, nausea, vomiting, epigastric distress, and diarrhea. The
severity of the epigastric distress and the diarrhea are dose related.
Headache, dizziness, insomnia, photophobia, tinnitus, and a tingling
sensation have been reported in some patients. |