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Linezolid

Linezolid


LINEZOLID

  • Synthetic antibiotic agent of oxazolidinone class of antibiotics.
  • Acts by inhibiting protein synthesis.
  • Used for treatment of serious infections due to multi-resistant Gram-positive bacteria.
  • Includes Methicillin-resistant Staphylococcus aureus (MRSA).
  • Vancomycin-resistant enterococci (VRE).
  • Also categorized under reversible, nonselective monoamine oxidase inhibitor. 
  • Hence, has potential for interaction with adrenergic & serotonergic agents.
MICROBIOLOGY:
  • In-vitro activity against aerobic gram-positive bacteria, certain gram-negative bacteria & anaerobic microorganisms.
  • Effective against all clinically important gram-positive bacteria.
  • Enterococcus faecium & Enterococcus faecalis (including vancomycin-resistant enterococci).
  • Staphylococcus aureus (including MRSA).
  • Streptococcus agalactiae, Streptococcus pneumoniae, & Streptococcus pyogenes
  • No effect on Gram-negative bacteria. 
  • Bacteriostatic – Against enterococci and staphylococci. 
  • Bactericidal – For streptococci for majority of strains. 
MECHANISM OF ACTION:

Protein synthesis inhibitor

  • Acts on first step of protein synthesis, Ie. ‘initiation’.
  • Unlike other protein synthesis inhibitors inhibiting elongation.
  • Binds to 23S portion of 50S subunit (center of peptidyl transferase activity).
  • Prevents formation of functional 70S-initiation complex. 
  • Linezolid resistance due to mutation of 23S ribosomal RNA has been detected among enterococci.

PHARMACOKINETICS:

  • Rapidly & completely absorbed orally.
  • Partly metabolized nonenzymatically.
  • Excreted in urine.
  • Plasma t½ – 5 hrs.
DOSAGE:
  • 600 mg BD, oral/ i.v..
  • Dose modification has not been necessary for renal insufficiency.

INDICATION:

  • Bacterial infections caused by susceptible strains of vancomycin-resistant Enterococcus faecium, Staphylococcal aureus (methicillin resistant and susceptible strains), Streptococcus pneumonia, Streptococcus pyogenes & Streptococcus agalactiae.
  • Community-Acquired Pneumonia (CAP)
  • Bacterial infections.
  • Skin & subcutaneous tissue bacterial infections
  • Uncomplicated skin & skin structure infections
  • Hospital-acquired bacterial pneumonia

 ADVERSE EFFECT:

  • Principal toxicity – Hematologic.
  • Is reversible & generally mild.
  • Thrombocytopenia – Most common manifestation.
  • Seen in approx. 3% of treatment courses.
  • Particularly when administered for longer than 2 weeks. 
  • Platelet count should be monitored.
  • Anaemia.
  • Neutropenia 
  • May underly bone marrow suppression.
  • Causes optic & peripheral neuropathy and lactic acidosis on prolonged use.
  • Due to linezolid-induced inhibition of mitochondrial protein synthesis.
DRUG INTERACTION:
  • Interactions seen with,
  • Adrenergic/Serotonergic drugs (SSRIs, etc.).
  • Excess dietary tyramine.
  • Because linezolid is MAO inhibitor.
Exam Question
 
  • Platelet count should be monitored in patient receiving linezolid therapy.
  • Optic neuropathy, Pancytopenia & Lactic acidosis are side effects of Linezolid.
  • In Methicillin-resistant Staphylococcus – aureus (MRSA) linezolid can be given.
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