Clinical and pharmacological group: & nbsp

Cephalosporins

Included in the formulation
  • Bestum
    powder w / m in / in 
    Vokhard Ltd     India
  • Witsef®
    powder w / m in / in 
    PREBAND PFC, LLC     Russia
  • Orzide®
    powder w / m in / in 
  • Tizim
    powder w / m in / in 
    Lupine Co., Ltd.     India
  • Fortazim®
    powdersolution w / m in / in 
  • Fortazim®
    powder w / m in / in 
  • Fortum
    powder for injections 
  • Cephzid
    powder w / m in / in 
    ELFA NPC, CJSC     Russia
  • Ceftazidime
    powdersolution in / in 
    KRASFARMA, JSC     Russia
  • Ceftazidime
    powdersolution w / m in / in 
  • Ceftazidime
    powdersolution w / m in / in 
    Company DEKO, LLC     Russia
  • Ceftazidime
    powder w / m in / in 
  • Ceftazidime
    powdersolution for injections 
  • Ceftazidime
    powdersolution w / m in / in 
    KRASFARMA, JSC     Russia
  • Ceftazidime
    powdersolution w / m in / in 
    PROTEK-SVM, LLC     Russia
  • Ceftazidime
    powdersolution w / m in / in 
  • Ceftazidime Kabi
    powdersolution w / m in / in 
  • Ceftazidime Kabi
    powdersolution d / infusion 
  • Ceftazidime Sandoz®
    powdersolution w / m in / in 
    Sandoz GmbH     Austria
  • Ceftazidime-AKOS
    powdersolution w / m in / in 
    SYNTHESIS, OJSC     Russia
  • Ceftazidime-Vial
    powdersolution w / m in / in 
    VIAL, LLC     Russia
  • Ceftazidime-Jodas
    powdersolution w / m in / in 
  • Ceftidine
    powdersolution w / m in / in 
    FARMGID CJSC     Russia
  • Included in the list (Order of the Government of the Russian Federation No. 2782-r of 30.12.2014):

    VED

    АТХ:

    J.01.D.D.02   Ceftazidime

    Pharmacodynamics:

    Cephalosporin antibiotic III generation for parenteral use.

    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 against gram-negative microorganisms: Pseudomonas spp., Escherichia coli, Klebsiella spp., Proteus mirabilis, Proteus vulgaris, Enterobacter spp., Citrobacter spp., Serratia spp., Haemophilus influenzae and Neisseria meningitidis; Gram-positive - Staphylococcus aureus, Streptococcus pyogenes, Streptococcus agalactiae and Streptococcus pneumoniae; anaerobic - Bacteroides spp.

    Resistant to the action of β-lactamases.

    Pharmacokinetics:

    After intravenous administration, the maximum concentration in the blood plasma is reached in 20-30 minutes, after intramuscular - in 1 hour. The connection with plasma proteins is 10%.

    Penetrates into all organs and tissues. Penetrates into the cerebrospinal fluid with meningitis. Do not cumulate. Not exposed to metabolism. Penetrates through the placental barrier, is found in breast milk.

    The half-life is 1.9 hours after intravenous administration and 2 hours after intramuscular injection. Elimination of the kidneys unchanged.

    Indications:

    It is used for treatment septicemia, peritonitis, meningitis, severe infections of the respiratory tract, urinary tract, skin, soft tissues, bones and joints, digestive tract, infections caused by Pseudomonas aeruginosa.

    I.A30-A49.A40   Streptococcal septicemia

    I.A30-A49.A41   Other septicemia

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

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

    X.J85-J86.J86   Pythothrace

    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

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

    Contraindications:

    Individual intolerance to β-lactam antibiotics: penicillins and cephalosporins.

    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:

    Use in children

    Intramuscularly and intravenously:

    up to 2 months: 25-50 mg / kg per day for 2 injections;

    over 2 months: 50-100 mg / kg per day.

    Adults

    Intravenous and intramuscular, 1 g every 8 hours or 2 g every 12 hours. In severe disease - up to 6 grams per day.

    The highest daily dose: 6 g.

    The highest single dose: 2 g.

    Side effects:

    Central and peripheral nervous system: rarely - convulsions.

    Hemopoietic system: thrombocytopenia, eosinophilia, leukopenia, increased prothrombin time and blood 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, convulsive attacks.

    Treatment is symptomatic, hemodialysis.

    Interaction:

    Simultaneous application with probenecid slows the renal excretion of ceftazidime.

    "Loop diuretics" block the tubular secretion of ceftazidime.

    Special instructions:

    Ceftazidime is not recommended for the treatment of meningitis.

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

    Instructions
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