Gentamicin

Brands: gentamicin

Out of stock

Dosing & Uses

ADULT and PEDIATRIC

Dosage Forms & Strengths

injectable solution

  • 10mg/mL
  • 40mg/mL

Intravenous solution

  • Intravenous solution
  • 60mg (50mL)
  • 70mg (50mL)
  • 80mg (50mL, 100mL)
  • 90mg (100mL)
  • 100mg (50mL, 100mL)
  • 120mg (100mL)

Susceptible Infections

Use of ideal body weight (IBW) for determining the mg/kg/dose appears to be more accurate than on the basis of total body weight (TBW)

Infants: 2.5 mg/kg/dose IV/IM q8hr

Children and adolescents:: 2-2.5 mg/kg/dose IV/IM q8hr  

<30 weeks' gestation

  • 0-28 days: 2.5 mg/kg/day IV/IM  
  • >28 days: 3 mg/kg/day IV/IM

30-36 weeks' gestation

  • 0-14 days: 3 mg/kg/day IV/IM  
  • >14 days: 5 mg/kg/day IV/IM divided q12hr

>36 weeks' gestation

  • 0-7 days: 5 mg/kg/day IV/IM divided q12hr  
  • >7 days: 7.5 mg/kg/day IV/IM divided q8hr

Surgical Prophylaxis, Preoperative (Off-label use)

2.5 mg/kg IV/IM within 60 min piror to surgical incision or without antibiotics; procedure dependent  

Dose is based on actual body weight unless >20% above ideal body weight; then dosage requirement may best be estimated using a dosing weight of IBW + 0.4 (TBW- IBW)

Dosage Modifications

GFR>50 mL/min/1.73m²: No dosage adjustment necessary

GFR 30-50 mL/min/1.73m²: Administer q12-18hr

GFR 10-29 mL/min/1.73m²: Administer q18-24hr

GFR <10 mL/min/1.73m² Administer q48-72hr

Intermitent hemodialysis: 2 mg/kg/dose; redose as indicated by serum concentration

Peritoneal dialysis: 2 mg/kg/dose; redose as indicated by serum concentration

Continuous renal replacement therapy: 2-2.5 mg/kg/dose q12-24hr; monitor serum concentration  

Dosing Considerations

Monitor peak (4-12 mg/L) and trough (1-2 mg/L)

Monitor nephrotoxicity, neurotoxicity, and ototoxicity; assess at beginning of therapy and throughout

Individualization critical due to low therapeutic index

Use ideal body weight for mg/kg/dose, except in neonates (in whom actual body weight should be used)

Bacterial organisms causing susceptible infections

  • Pseudomonas aeruginosa
  • Proteus species (indole-positive and indole-negative)
  • Escherichia coli
  • Klebsiella-Enterobacter-Serratia species
  • Citrobacter species
  • Staphylococcus species (coagulase-positive and coagulase-negative)

Adverse Effects

>10%

Neurotoxicity (vertigo, ataxia)

Gait instability

Ototoxicity (auditory, vestibular)

Nephrotoxicity (decreased CrCl)

Nephrotoxicity if trough >2 mg/L

1-10%

Edema

Rash

Reddening of skin

Itching

<1%

Drowsiness

Headache

Pseudomotor cerebri

Photosensitivity

Allergic reaction

Erythema

Anorexia

Nausea/vomiting

Weight loss

Increased salivation

Enterocolitis

Granulocytopenia

Agranulocytosis

Thrombocytopenia

Elevated LFTs

Burning

Stinging

Tremors

Muscle cramps

Weakness

Dyspnea

Contraindications

Prior aminoglycoside toxicity or hypersensitivity

Cautions

Patients treated withaminoglycosides should be under close clinical observation; high risk of toxicity associated with their use

Risk of ototoxicity; tinnitus or vertigo may be indications of vestibular injury and impending bilateral irreversible damage; discontinue therapy if signs of ototoxicity occur

Risk of nephrotoxicity; other factors that increase patient risk of ototoxicity include advanced age and dehydration

Narrow therapeutic index (not intended for long-term therapy)

Caution in renal failure (not on dialysis), myasthenia gravis, hypocalcemia, and conditions that depress neuromuscular transmission

Adjust dose in renal impairment

Endocarditis prophylaxis (GI, GU procedure): AHA Guidelines recommend only for high-risk patients

Diuretics may enhance aminoglycoside toxicity by altering antibiotic concentration in serum and tissue; certain diuretics by themselves may cause ototoxicity; avoid potent diuretics, including ethacrynic acid or furosemide

Use caution in patients with electrolyte abnormalitie including hypocalcemia, hypomagnesemia, or hypokelemia

Use caution in patients with neuromuscular disorders, including myasthenia gravis

Use caution in patients with hearing and renal impairment

Pregnancy & Lactation

Pregnancy category: D

Lactation: Enters breast milk; use with caution (AAP Committee states "compatible with nursing")

Pregnancy Categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

 

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

 

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

 

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.