Clinical and pharmacological group: & nbsp

Cephalosporins

Included in the formulation
  • Kefepim
    powdersolution w / m in / in 
  • Maxipim®
    powdersolution w / m in / in 
  • Maxitsef®
    powder w / m in / in 
    PREBAND PFC, LLC     Russia
  • Movizar
    powder w / m in / in 
  • Tsepim
    powdersolution w / m in / in 
    SYNTHESIS, OJSC     Russia
  • Cefepim
    powdersolution w / m in / in 
  • Cefepim
    powdersolution w / m in / in 
    BIOSINTEZ, PAO     Russia
  • Cefepim
    powdersolution w / m in / in 
    NIZHFARM, JSC     Russia
  • Cefepim
    powdersolution w / m in / in 
  • Cefepim
    powdersolution w / m in / in 
    Company DEKO, LLC     Russia
  • Cefepim
    powdersolution w / m in / in 
  • Cefepim
    powdersolution w / m in / in 
    KRASFARMA, JSC     Russia
  • Cefepim
    powdersolution w / m in / in 
    KRASFARMA, JSC     Russia
  • Cefepim
    powdersolution w / m in / in 
  • Cefepim
    powder w / m in / in 
  • Cefepim
    powder w / m in / in 
  • Cefepim
    powder w / m in / in 
    KRASFARMA, JSC     Russia
  • Cefepim-Alkem
    powdersolution w / m in / in 
  • Cefepime-Vial
    powdersolution w / m in / in 
  • Cephepim-Jodas
    powdersolution w / m in / in 
    JODAS EKSPOIM, LLC     Russia
  • Cefomax
    powdersolution w / m in / in 
  • Etipim®
    powdersolution w / m in / in 
       
  • Etipim®
    powdersolution w / m in / in 
       
  • Included in the list (Order of the Government of the Russian Federation No. 2782-r of 30.12.2014):

    VED

    АТХ:

    J.01.D.E.01   Cefepim

    Pharmacodynamics:

    Has bactericidal action due to inhibition of bacterial cell wall synthesis. Violates the synthesis of the biopolymer peptidoglikana - the main component of the cell wall of bacteria. It inhibits the peptidoglycan transpeptidase, inhibits the activity of the endogenous inhibitor, which leads to activation of murein hydrolase, which cleaves peptidoglycan. Effective against fissile bacteria, in the walls of which the synthesis of peptidoglycan occurs.

    Active with gram-positive: Staphylococcus aureus, Staphylococcus epidermidis, S. hominis, S. saprophyticus, Streptococcus pyogenes (group A), Streptococcus agalactiae (group B), Streptococcus pneumoniae other β-hemolytic streptococci (groups C, G, F), S. bovis (group D), S. Viridans; Gram-negative aerobes: Pseudomonas spp., Enterobacter spp. (including E. cloacae, E. aerogenes, E. agglomerans, E. sakazakii), Proteus spp., Acinetobacter calcoaceticus (subsp. Anitratus, Iwofii), Aeromonas hydrophila, Capnocytophaga spp., Citrobacter spp, Campylobacter jejuni, Gardnerella vaginalis, Haemophilus ducreyi, Haemophilus influenzae, Haemophilus parainfluenzae, Hafnia alvei, Legionella spp., Morganella morganii, Moraxella catarrhalis, Neisseria gonorrhoeae, Neisseria meningitidis, Providencia spp., Salmonella spp ., Serratia, Shigella spp., Yersinia enterocolitica; a also anaerobes: Bacteroides spp., Clostridium perfringens, Fusobacterium spp., Mobiluncus spp., Peptostreptococcus spp., Veillonella spp.

    Inactive at respect Bacteroides fragilis and Clostridium difficile.

    Highly resistant to hydrolysis by most β-lactamases, especially chromosome-mediated ones.

    Pharmacokinetics:

    After intramuscular injection, the maximum concentration in the blood plasma is reached after 30-120 minutes, after intravenous administration - after 10 minutes. It binds to plasma proteins up to 19%.

    Not exposed to metabolism. Penetrates through the placental and blood-brain barrier (with inflammatory changes in the meninges) barrier, found in breast milk.

    The elimination half-life is 2 hours, during hemodialysis, the half-life is 13 hours, with continuous ambulatory peritoneal dialysis - 19 hours.

    Elimination of the kidneys unchanged.

    Indications:

    It is used to treat infections caused by pathogens that are sensitive to cefepime: respiratory tract, including pneumonia and bronchitis, urinary tract, skin and soft tissues, intra-abdominal infections, including peritonitis and bile duct infections. It is used for gynecological infections, septicemia, for the purpose of empirical treatment for febrile neutropenia.

    I.A30-A49.A39   Meningococcal infection

    I.A30-A49.A40   Streptococcal septicemia

    I.A30-A49.A41   Other septicemia

    VI.G00-G09.G00   Bacterial meningitis, not elsewhere classified

    X.J00-J06.J00   Acute nasopharyngitis (runny nose)

    X.J30-J39.J31.1   Chronic nasopharyngitis

    X.J30-J39.J31   Chronic rhinitis, nasopharyngitis and pharyngitis

    X.J00-J06.J01   Acute Sinusitis

    X.J30-J39.J32.9   Chronic sinusitis, unspecified

    X.J30-J39.J31.2   Chronic pharyngitis

    X.J00-J06.J02   Acute pharyngitis

    X.J00-J06.J03   Acute tonsillitis

    X.J30-J39.J35.0   Chronic tonsillitis

    X.J00-J06.J04   Acute laryngitis and tracheitis

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

    X.J20-J22.J20   Acute bronchitis

    X.J40-J47.J42   Chronic bronchitis, unspecified

    X.J40-J47.J40   Bronchitis, not specified as acute or chronic

    XI.K65-K67.K65.0   Acute peritonitis

    XI.K80-K87.K81.1   Chronic cholecystitis

    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

    XIII.M00-M03.M00   Pyogenic arthritis

    XIII.M86-M90.M86   Osteomyelitis

    XIV.N10-N16.N11   Chronic tubulointerstitial nephritis

    XIV.N10-N16.N10   Acute tubulointerstitial nephritis

    XIV.N30-N39.N30   Cystitis

    XIV.N30-N39.N34   Urethritis and urethral syndrome

    XIV.N40-N51.N41   Inflammatory diseases of the prostate

    XIV.N70-N77.N70   Salpingitis and oophoritis

    XIV.N70-N77.N71.0   Acute inflammatory disease of the uterus

    XIV.N70-N77.N72   Inflammatory disease of the cervix

    XIV.N70-N77.N73.0   Acute parametritis and pelvic cellulite

    Contraindications:

    Individual intolerance of β-lactam antibiotics: penicillins and cephalosporins, neonatal period.

    Carefully:

    Imbalance of electrolytes or fluids, severe liver damage, colitis in history.

    Pregnancy and lactation:

    Recommendations for FDA - Category B. It is used in pregnancy and lactation.

    Dosing and Administration:

    Use in children

    Intramuscularly, from the age of two months with a body weight of up to 40 kg - 50 mg / kg every 12 hours, with severe infections - every 8 hours.

    Adults

    Intravenously slowly or intramuscularly, intraglutally, 0.5-1 g (in severe infections - 2 g) every 12 hours, with severe disease - every 8 hours.

    The highest daily dose: 4 g.

    The highest single dose: 2 g.

    Side effects:

    Central and peripheral nervous system: headache, asthenia, paresthesia, confusion, hallucinations (with inflammatory phenomena of the meninges), rarely - convulsions.

    Respiratory system: cough.

    Hemopoietic system: thrombocytopenia, eosinophilia, leukopenia, an increase in prothrombin index and coagulation time.

    Digestive system: nausea, vomiting, diarrhea, increased activity of hepatic enzymes, hepatic or cholestatic jaundice, intestinal dysbacteriosis.

    Dermatological reactions: local reactions - compaction at the injection site, candidiasis dermatitis, vulvovaginitis.

    urinary system: rarely - the development of hypokalemia.

    Allergic reactions.

    Overdose:

    Nausea, vomiting, diarrhea, neuromuscular excitability, encephalopathy, convulsive attacks.

    Treatment is symptomatic, hemodialysis.

    Interaction:

    Increases the nephro- and ototoxicity of aminoglycosides, furosemide and other loop diuretics.

    Simultaneous application with probenecid slows the renal excretion of cefepime.

    "Loop diuretics" block the tubular secretion of cefepime.

    Special instructions:

    Simultaneous use with ethanol can cause a disulfiram-like reaction.

    Instructions
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