section name header

Pronunciation ⬇

jen-ta-MYE-sin

Classifications ⬆ ⬇

Therapeutic Classification: anti-infectives

Pharmacologic Classification: aminoglycosides

Indications ⬆ ⬇

REMS


Action ⬆ ⬇

  • Inhibits protein synthesis in bacteria at level of 30S ribosome.
Therapeutic effects:
  • Bactericidal action.

Spectrum:

Pharmacokinetics ⬆ ⬇

Absorption: Well absorbed after IM administration. IV administration results in complete bioavailability. Some absorption follows administration by other routes.

Distribution: Widely distributed throughout extracellular fluid; crosses the placenta; small amounts enter breast milk. Poor penetration into CSF.

Metabolism/Excretion: >90% excreted unchanged by kidneys.

Half-Life: Neonates <7 days: 3–11.5 hr; Neonates 7–30 days: 3–6 hr; Infants: 3–5 hr; Children: 1–3 hr; Adolescents: 0.5–2.5 hr; Adults: 2–4 hr (↑ in renal impairment).

Time/Action Profile ⬆ ⬇

(blood levels‡)
ROUTEONSETPEAKDURATION
IMrapid30–90 min8–24 hr
IVrapid15–30 min‡8–24 hr

‡All parenterally administered aminoglycosides.

‡Post-distribution peak occurs 30 min after the end of a 30-min infusion and 15 min after the end of a 1-hr infusion.



Contraind./Precautions ⬆ ⬇

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects ⬆ ⬇

EENT: ototoxicity (vestibular and cochlear)

GU: nephrotoxicity

MS: muscle paralysis (high parenteral doses)

Neuro: ataxia, vertigo

Misc: hypersensitivity reactions

Interactions ⬆ ⬇

Drug-drug:

Route/Dosage ⬆ ⬇

Renal Impairment

Availability ⬆ ⬇

(Generic available)

Assessment ⬆ ⬇

Lab Test Considerations:

Toxicity and Overdose:

Implementation ⬆ ⬇

IV Administration:

Patient/Family Teaching ⬆ ⬇

Evaluation/Desired Outcomes ⬆ ⬇

US Brand Names ⬆

Garamycin