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cefuroxime 500 mg + potassium clavunate 125 mg tab

cefuroxime 500 mg + potassium clavunate 125 mg tab

Product Details:

  • Drug Type Other Types
  • Ingredients Cefuroxime Axetil 500 mg + clavulanate potassium 125 mg
  • Physical Form Tablets
  • Function Antibiotic Medicine
  • Recommended For ALL AGE
  • Dosage Guidelines As directed by the physician
  • Quantity 500 Boxes
  • Supply Ability : as per market demands Per Day Per Year
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Price And Quantity

  • 500 Box
  • 1 INR
  • 1.00 - 1.00 INR

Product Specifications

  • As directed by the physician
  • Cefuroxime Axetil 500 mg + clavulanate potassium 125 mg
  • Antibiotic Medicine
  • 500 Boxes
  • ALL AGE
  • Other Types
  • store in a cool & dry ,dark plase
  • Tablets

Trade Information

  • Cash Against Delivery (CAD), Cash on Delivery (COD)
  • as per market demands Per Day Per Year
  • 45 Days
  • Within a certain price range free samples are available
  • 1*6 , 1*10
  • All India
  • Drug Licence, WHO GMP Certified,

Product Description

efuroxime 500mg + Clavulanic acid 125mg Salt Information :

Uses of Cefuroxime 500mg + Clavulanic acid 125mg:

Cefuroxime is a cephalosporin antibiotic. Cefuroxime is used in the treatment of various bacterial infections. Cefuroxime is used in infections of respiratory tract infections like pharyngitis, otitis media, sinusitis, and bronchitis.

Side Effects of Cefuroxime 500mg + Clavulanic acid 125mg:

Large doses can cause cerebral irritation and convulsions; nausea, vomiting, diarrhoea, GI disturbances; erythema multiforme, Stevens-Johnson syndrome, epidermal necrolysis.Potentially Fatal: Anaphylaxis, nephrotoxicity, pseudomembranous colitis.

Drug Interactions of Cefuroxime 500mg + Clavulanic acid 125mg:

Probenecid decreases renal clearance of cefuroxime.Potentially Fatal: Nephrotoxicity with aminoglycosides and furosemide.

Contraindications of Cefuroxime 500mg + Clavulanic acid 125mg:

Hypersensitivity to cephalosporins.

Mechanism of Action of Cefuroxime 500mg + Clavulanic acid 125mg:

Cefuroxime binds to one or more of the penicillin-binding proteins (PBPs) which inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell wall, thus inhibiting biosynthesis and arresting cell wall assembly resulting in bacterial cell death.Absorption: Absorbed from the GI tract with peak plasma concentrations after 2-3 hr (oral); may be enhanced by the presence of food.Distribution: Pleural and synovial fluid, sputum, bone and aqueous fluids; CSF (therapeutic concentrations). Crosses the placenta and enters breast milk. Protein-binding: Up to 50%.Metabolism: Rapidly hydrolysed (intestinal mucosa and blood).Excretion: Via the urine by glomerular filtration and renal tubular secretion (as unchanged); via bile (small amounts); 70 min (elimination half-life); prolonged in neonates and renal impairment.

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