Clinical and pharmacological group: & nbsp

Aminoglycosides

Included in the formulation
  • Gentamicin
    drops d / eye 
  • Gentamicin
    solution w / m in / in 
  • Gentamicin
    powder w / m 
  • Gentamicin
    solution w / m in / in 
    OMELA, LTD.     Russia
  • Gentamicin
    solution w / m in / in 
  • Gentamicin
    drops d / eye 
  • Gentamicin
    solution w / m in / in 
    DALHIMFARM, OJSC     Russia
  • Gentamicin
    solution w / m in / in 
    Company DEKO, LLC     Russia
  • Gentamicin
    solution w / m in / in 
  • Gentamicin
    ointment externally 
    NIZHFARM, JSC     Russia
  • Gentamicin
    solution w / m in / in 
  • Gentamicin
    solution w / m in / in 
  • Gentamycin-AKOS
    ointment externally 
    SYNTHESIS, OJSC     Russia
  • Gentamicin-K
    solution w / m in / in 
  • Gentamicin-Ferein®
    drops d / eye 
    BRYNTSALOV-A, CJSC     Russia
  • Gentamicin-Ferein®
    solution w / m in / in 
    BRYNTSALOV-A, CJSC     Russia
  • Gentamicin Sulfate
    solution w / m in / in 
    Mapichem AG     Switzerland
  • Included in the list (Order of the Government of the Russian Federation No. 2782-r of 30.12.2014):

    VED

    АТХ:

    J.01.G.B.03   Gentamicin

    Pharmacodynamics:

    Antibiotic from the group of aminoglycosides. Linked from 30S-subunit of the ribosomes of the bacterial cell and disrupts the movement of the ribosome along the filaments PHK. Also changes the process of reading the code PHK, which leads to the synthesis of functionally inactive proteins. Is able to disrupt the permeability of the cytoplasmic membrane of microorganisms. Has a bactericidal type of action against Neisseria gonorrhoeae, including strains producing penicillinase.

    Pharmacokinetics:

    With intramuscular injection gentamicin quickly absorbed: bactericidal concentration in the blood serum is achieved 1 hour after the injection and persists for 8-12 hours. With intravenous drip introduction, the concentration of antibiotic in the blood plasma during the first hours exceeds the concentration that is reached by intramuscular injection of the drug. The connection with plasma proteins is about 10%. Not exposed to metabolism. Penetrates through the planetary barrier.

    The half-life is 2-4 hours. Elimination by the kidneys.

    Indications:

    It is used to treat bacterial infections caused by sensitive microorganisms: infections of the upper and lower respiratory tract (including bronchitis, pneumonia, pleural empyema), complicated urogenital infections (including pyelonephritis, cystitis,urethritis, prostatitis, endometritis), bone and joint infections (including osteomyelitis), skin and soft tissue infections, abdominal infections (peritonitis, pelvic inflammation), infections of the central nervous system (including meningitis), gonorrhea, sepsis, wound and burn infection, otitis.

    I.A30-A49.A40   Streptococcal septicemia

    I.A30-A49.A41   Other septicemia

    X.J10-J18.J13   Pneumonia caused by Streptococcus pneumoniae

    X.J10-J18.J15   Bacterial pneumonia, not elsewhere classified

    X.J85-J86.J86   Pythothrace

    XI.K65-K67.K65   Peritonitis

    XI.K80-K87.K81.0   Acute cholecystitis

    XI.K80-K87.K83.0   Cholangitis

    XII.L00-L08.L01   Impetigo

    XII.L00-L08.L02   Abscess of skin, boil and carbuncle

    XII.L00-L08.L03   Phlegmon

    XII.L00-L08.L08.0   Pyoderma

    XII.L20-L30.L21   Seborrheic dermatitis

    XII.L60-L75.L73.8   Other specified diseases of follicles

    XIII.M00-M03.M00   Pyogenic arthritis

    XIII.M86-M90.M86   Osteomyelitis

    XIV.N10-N16.N10   Acute tubulointerstitial nephritis

    XIV.N10-N16.N11   Chronic tubulointerstitial nephritis

    XIV.N30-N39.N30   Cystitis

    XIX.T20-T32.T30   Thermal and chemical burns, unspecified

    XIX.T79.T79.3   Post-traumatic wound infection, not elsewhere classified

    Contraindications:

    Severe renal failure with azotemia (residual nitrogen in the blood above 150 mg%) and uremia, diseases of auditory and vestibular, cochlear neuritis, myasthenia gravis, idiosyncrasy.

    Carefully:

    Botulism, parkinsonism, myasthenia gravis, renal failure, dehydration, neonatal period, prematurity of children, advanced age.

    Pregnancy and lactation:

    Recommendations for FDA - category D. Contraindicated during pregnancy and lactation.

    Dosing and Administration:

    Use in children

    Newborns and infants: 6-7 mg / kg per day.

    Older than 2 years: 1.2-5 mg / kg per day in 2-3 injections.

    Adults

    Intramuscularly: 3 mg / kg body weight in 2-3 injections.

    Intravenously: 3 mg / kg body weight in 5-15 ml sodium chloride solution 0,9% or 5% glucose solution.

    The highest daily dose: 5 mg / kg.

    The highest single dose: 3 mg / kg.

    Side effects:

    Central and peripheral nervous system: neuromuscular blockade, respiratory arrest.

    Digestive system: candidiasis, nausea, vomiting, malabsorption syndrome.

    Sense organs: deafness.

    Urinary system: toxic nephrosis.

    Dermatological reactions: Candidiasis, itching, burning with local application.

    Allergic reactions.

    Overdose:

    Stop breathing.

    Treatment: hemodialysis, oxygen therapy, anticholinesterase drugs, calcium salts.

    Interaction:

    Simultaneous use with anesthetics, inhalation of halogenated hydrocarbons, blockers of neuromuscular transmission, massive transfusions of citrated blood increases the risk of blockade of neuromuscular transmission.

    Simultaneous use with warfarin enhances the therapeutic effect.

    When used simultaneously with other aminoglycosides, the risk of ototoxicity increases.

    The risk of nephrotoxicity increases with simultaneous use with amphotericin B, aldesleukin, salicylates, acyclovir, bacitracin, carmustine, ifosfamide, preparations of gold and lithium, sulfonamides, cytostatics.

    Special instructions:

    When parenteral administration can sometimes cause the development of curare-like symptoms.

    Instructions
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