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CANSPAR

Contains
  • Indication

    Community-acquired pneumonia, Acute bacterial exacerbation of chronic bronchitis

  • Dosage

    Oral Community-acquired pneumonia, Acute bacterial exacerbation of chronic bronchitis Adult: 100-300 mg daily, as a single dose or 2 divided doses. Renal impairment: Dosage adjustment may be necessary in severe impairment.

  • Administration

    May be taken with or without food.

  • Contraindications

    Hypersensitivity; pregnancy and lactation; children <18 yr.

  • Special precautions

    Hypersensitivity; pregnancy and lactation; children <18 yr.

  • Adverse drug reactions

    Diarrhoea, abdominal pain, nausea, vomiting; jaundice, renal failure, elevation of liver enzymes, BUN and creatinine; anaphylactoid reaction, headache, dizziness, convulsions; tremors, myalgia; rhabdomyolysis, thrombocytopenia and eosinophilia. Potentially Fatal: AV block; anaphylaxis.

  • Drug interaction

    Cations such as aluminum, magnesium, zinc and iron may reduce the bioavailability of sparfloxacin. May increase the plasma concentrations of theophylline and tizanidine. May enhance the effect of warfarin and glibenclamide. May decrease the renal clearance of methotrexate. Excretion may be reduced by probenecid. May alter serum levels of phenytoin. Potentially Fatal: Corticosteroids may increase risk of tendon rupture. Increased risk of seizures with NSAIDs. Risk of additive QT prolongation effect when used with class Ia or III antiarrhythmic drugs, astemizole,terfenadine, cisapride, erythromycin, pentamidine, phenothiazines or TCAs.

  • Mech of action

    Sparfloxacin inhibits the supercoiling activity of DNA gyrase which is an enzyme essential for DNA replication thus promoting the breakage of DNA structures. It has activity against S. pneumoniae, S. aureus, H. influenzae, K. pneumoniae, M. catarrhalis and Mycobacterium spp. Absorption: Well absorbed from the GI tract (oral); peak plasma concentrations after 3-6 hr. Distribution: Widely distributed into tissues including respiratory tissues. Protein-binding: 45%. Metabolism: Hepatic (by glucuronidation). Excretion: Excreted in equal amounts in the urine and faeces as unchanged drug and glucuronide metabolites; elimination half-life: 20 hr.

  • CIMS class

    Quinolones

  • ATC class

    J01MA09 - sparfloxacin; Belongs to the class of quinolones, fluoroquinolone. Used in the treatment of systemic infections.

  • Additional Info

    *sparfloxacin information: Note that there are some more drugs interacting with sparfloxacin sparfloxacin sparfloxacin brands available in India Always prescribe with Generic Name : sparfloxacin, formulation, and dose (along with brand name if required)

 
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