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Gentamicin

Gentamicin, sold under brand names Garamycin among others, is an antibiotic used to treat several types of bacterial infections. More

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Description

Gentamicin, sold under brand names Garamycin among others, is an antibiotic used to treat several types of bacterial infections.

Generic Name

Gentamicin

Chemical names

Gentamicin; Garamycin; Gentacycol; GENTAMYCIN; Gentavet

Brand names

Bactigen, Belar-G, Biogaracin, Candigen-BG, Clobetamil-G, Cloma-G, Clotech-GMZ, Cortisol-G, Dermonit, Dipgenta, Diprovate-G, Emugent DPS, Enderm-GM, G-Mycin, G.Mycin E/E, G20/80, Garamax, Garamycin INJ, Geco, Gem, Gem INJ, Genbiotic, Genka, Genkind, Genmycin, Gensat, Genster, Genta Cort-D, Genta Swift, Genta Swift E/E, Genta Swift-D, Gentacip, Gentacip-D, Gentacort-FC, Gentacort-MF, Gentact, Gentafast, Gentalab, Gentalab DPS, Gentam, Gentamicin, Gentamicin INJ, Gentamicin Sulphate, Gentamycin, Gentamycin INJ, Gentaril, Gentasia, Gentasia-D, Gentasporin, Gentasporin E/E

IUPAC name

2-{[4,6-diamino-3-({3-amino-6-[1-(methylamino)ethyl]oxan-2-yl}oxy)-2-hydroxycyclohexyl]oxy}-5-methyl-4-(methylamino)oxane-3,5-diol

Pharmacokinetics

Poor absorption.

Actions

Gentamicin is a broad spectrum aminoglycoside antibiotic act by binding to the bacterial 30S ribosomal subunit, causes misreading of t-RNA, leaving the bacterium unable to synthesize proteins vital to its growth. Aminoglycosides are useful primarily in infections involving aerobic, Gram-negative bacteria, such as Pseudomonas, Acinetobacter, and Enterobacter. 

Dosage/Dosage form

The recommended dose is 1.5-2 mg/kg loading dose followed by 1-1.7 mg/kg every 8 hours or 5-7 mg/kg every 24 hours.

Therapeutic uses

P. aeruginosaProteus species (indole-positive and indole-negative), E. coliKlebsiella-Enterobactor-Serratia species, Citrobacter species and Staphylococcus species (coagulase-positive and coagulase-negative), these stains will be treated by gentamicin.

Adverse effects/Side effects

Dizziness or vertigo; acute renal failure, interstitial nephritis, acute tubular necrosis; electrolyte imbalances; transient elevation of serum bilirubin and aminotransferases; purpura; nausea, vomiting; convulsions, mental depression, hallucinations. Atrophy or rat necrosis at inj sites. Nephrotoxicity, ototoxicity and neuromuscular blockade

Interaction

  • Cephalosporins, cisplatin, ciclosporin, vancomycin, hydrocortisone and indometacin potentiate nephrotoxicity.
  • When combined with ethacrynic acid and furosemide incidence of ototoxicity increased.
  • Potentiates neuromuscular blocking agents.
  • Synergistic with ampicillin, benzylpenicillin and other β-lactam antibiotics.
  • Increased risk of severe respiratory depression when used concurrently with anaesthetics or opioids.
  • when used with biphosphonates may induce hypocalcaemia and reduce renal clearance of zalcitabine
  • Not to be used with agalsidase alfa or beta as it may inhibit α-galactosidase activity.

Contraindications

Pregnancy; History of hypersensitivity to aminoglycoside; perforated ear drum. Hepatic impairment.

Storage

Store at 15-30°C.

Information

Molecular weight

477.5954

Molecular formula

C21H43N5O7

CAS number

1403-66-3

Precautions

  • Concurrent use of neuromuscular blocking agents; myasthenia gravis, Parkinsonism; conditions predisposing to ototoxicity and nephrotoxicity; lactation.
  • Plasma concentrations of this drug will have to monitor in infants, patients who is receiving high doses or prolonged courses, in elderly, and patients with renal impairment, cystic fibrosis or significant obesity.
  • Monitor auditory and renal functions.