Clinical and pharmacological group: & nbsp

Cephalosporins

Included in the formulation
  • Isodep®
    powder w / m in / in 
       
  • Cephanorm
    powdersolution w / m in / in 
  •    
  • АТХ:

    J.01.D.E.02   Tsefpyrom

    Pharmacodynamics:

    Antibiotic group cephalosporins of the IV generation. 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.

    Has a wide spectrum of action against gram-positive and gram-negative bacteria, strains resistant to cephalosporin antibiotics of the third generation and aminoglycosides. Active with respect to E. coli, Salmonella spp., Shigella spp., Proteus mirabilis, Proteus vulgaris, Providencia, Morganella morganii, Citrobacter diversus, Citrobacter freundii, Klebsiella oxytoca, Serratia spp., Enterobacter spp., Haemophilus influenzae, Neisseria spp., Moraxella catarrhalis, Streptococcus spp., Staphylococcus spp., Peptostreptococcus spp., Clostridium perfringens, Ps. aeruginosa.

    Pharmacokinetics:

    After intravenous administration, the maximum concentration in the blood plasma is reached after 5 minutes. The connection with plasma proteins is about 10%.

    Penetrates into all organs and tissues. When meningitis gets into the cerebrospinal fluid.It is subject to partial metabolism in the liver. Do not cumulate. Penetrates through the placental barrier, is found in breast milk.

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

    Indications:

    It is used to treat infections caused by susceptible microorganisms cefpirome, including in patients with neutropenia and immunocompromised: septicemia, bacteremia, complicated infections of the upper and lower parts of the urinary system, pneumonia, lung abscess, empyema, skin and soft tissue infections.

    I.A30-A49.A40   Streptococcal septicemia

    I.A30-A49.A41   Other septicemia

    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

    X.J85-J86.J85   Abscess of the lung and mediastinum

    X.J85-J86.J86   Pythothrace

    X.J90-J94.J90   Pleural effusion, not elsewhere classified

    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

    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

    XIV.N70-N77.N75   Diseases of the Bartholin gland

    XXI.Z20-Z29.Z29.2   Another type of preventive chemotherapy

    Contraindications:

    Individual intolerance of β-lactam antibiotics: penicillins and cephalosporins, children under 12 years.

    Carefully:

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

    Pregnancy and lactation:

    Recommendations for FDA - Category B. It is used with caution during pregnancy and lactation in cases where the intended benefit exceeds the risk to the fetus and newborn.

    Dosing and Administration:

    Intravenously struino, slowly or infuzionno, 1-2 g every 12 hours. Patients on hemodialysis receive 500 mg per day with an additional 250 mg after each procedure.

    The highest daily dose: 2 g.

    The highest single dose: 2 g.

    Side effects:

    Central and peripheral nervous system: rarely - convulsions.

    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:

    Convulsions, tremor, increased neuromuscular excitability, encephalopathy (especially with renal failure).

    Treatment: hemodialysis (within 4 hours is eliminated 40-45%) and symptomatic treatment.

    Interaction:

    Simultaneous application with probenecid slows the renal excretion of cefpirom.

    "Loop diuretics" block the tubular secretion of ceftirom.

    Special instructions:

    Ceftir is not recommended for the treatment of meningitis.

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

    Instructions
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