Active substanceCeftriaxoneCeftriaxone
Similar drugsTo uncover
  • Azaran
    powdersolution w / m in / in 
    Hemofarm AD     Serbia
  • Axon
    powder w / m in / in 
  • Betasporin
    powdersolution w / m in / in 
    Laboratorios Atral SA     Portugal
  • Biotrakson
    powdersolution w / m in / in 
  • Broadssef-S
    powdersolution w / m in / in 
    ELFA NPC, CJSC     Russia
  • IFICEF®
    powder w / m in / in 
  • Lendacin®
    powder d / infusion 
    Lek dd     Slovenia
  • Lifaxon
    powdersolution w / m in / in 
    FARMGID CJSC     Russia
  • Medaxon
    powder w / m in / in 
    Medocemi Co., Ltd.     Cyprus
  • Movigip®
    powder w / m in / in 
  • Oframax®
    powdersolution w / m in / in 
  • Rocefin®
    powder w / m 
    Hoffmann-La Roche Ltd.     Switzerland
  • Rocefin®
    powder in / in 
  • Rocefin®
    powder w / m in / in 
    Hoffmann-La Roche Ltd.     Switzerland
  • Rocefin®
    powder d / infusion 
    Hoffmann-La Roche Ltd.     Switzerland
  • Steritsef®
    powdersolution for injections 
  • Tertsef®
    powdersolution w / m in / in 
    Aktavis, AO     Iceland
  • TOROCEF®
    powdersolution w / m in / in 
  • Triacson
    powdersolution w / m in / in 
  • Chizon
    powdersolution w / m in / in 
    Shin Pung Pharmaceutical Co., Ltd.     The Republic of Korea
  • Cefaxon
    powdersolution w / m in / in 
    Lupine Co., Ltd.     India
  • Cefatrine
    powdersolution w / m in / in 
  • Cefogram®
    powdersolution w / m in / in 
  • Cepheon
    powdersolution w / m in / in 
  • Cepheon
    powdersolution w / m in / in 
  • Ceftriabol®
    powdersolution w / m in / in 
    PREBAND PFC, LLC     Russia
  • Ceftriabol®
    powdersolution w / m in / in 
    PREBAND PFC, LLC     Russia
  • Ceftriaxone
    powdersolution d / infusion 
    KRASFARMA, JSC     Russia
  • Ceftriaxone
    powdersolution w / m in / in 
    KRASFARMA, JSC     Russia
  • Ceftriaxone
    powdersolution w / m in / in 
    BELMEDPREPARATY, RUP     Republic of Belarus
  • Ceftriaxone
    powdersolution w / m in / in 
    RUZFARMA, LLC     Russia
  • Ceftriaxone
    powdersolution w / m in / in 
    RAFARMA, CJSC     Russia
  • Ceftriaxone
    powdersolution
    Mapichem AG     Switzerland
  • Ceftriaxone
    powdersolution w / m in / in 
    BIOSINTEZ, PAO     Russia
  • Ceftriaxone
    powdersolution w / m in / in 
  • Ceftriaxone
    powdersolution w / m in / in 
    LEKKO, ZAO     Russia
  • Ceftriaxone
    powdersolution w / m in / in 
  • Ceftriaxone
    powdersolution w / m in / in 
    Vertex Exports     India
  • Ceftriaxone
    powdersolution w / m in / in 
    BIOCHEMIST, OJSC     Russia
  • Ceftriaxone
    powdersolution w / m in / in 
  • Ceftriaxone
    powdersolution w / m in / in 
  • Ceftriaxone
    powdersolution
    SYNTHESIS, OJSC     Russia
  • Ceftriaxone
    powdersolution w / m in / in 
    Company DEKO, LLC     Russia
  • Ceftriaxone
    powdersolution w / m in / in 
    MAKIZ-PHARMA, LLC     Russia
  • Ceftriaxone
    powder w / m in / in 
    HIMFARM, JSC     Kazakhstan
  • Ceftriaxone
    powder w / m in / in 
  • Ceftriaxone Danson
    powdersolution w / m in / in 
  • Ceftriaxone DS
    powdersolution
  • Ceftriaxone Kabi
    powdersolution w / m in / in 
  • Ceftriaxone Kabi
    powdersolution w / m in / in 
  • Ceftriaxone Protek
    powdersolution w / m in / in 
  • Elf Ceftriaxone
    powdersolution w / m in / in 
    ELFA NPC, CJSC     Russia
  • Ceftriaxone-Vial
    powdersolution w / m in / in 
    VIAL, LLC     Russia
  • Ceftriaxone-Jodhas
    powdersolution w / m in / in 
  • Ceftriaxone-CmP
    powdersolution w / m in / in 
  • Ceftriaxone-LEXMM®
    powdersolution w / m in / in 
  • Dosage form: & nbspPowder for the preparation of solution for intramuscular and intravenous administration.
    Composition:Active substance: Ceftriaxone sodium (equivalent to ceftriaxone) 0.25 g, 0.5 g or 1 g.
    Description:Crystalline powder from white to light yellow.
    Pharmacotherapeutic group:Antibiotic-cephalosporin.
    ATX: & nbsp

    J.01.D.D.04   Ceftriaxone

    Pharmacodynamics:

    Ceftriaxone is a third generation cephalosporin antibiotic for parenteral use, has a bactericidal effect, inhibits the synthesis of the cell membrane, in vitro suppresses the growth of most gram-positive and gram-negative microorganisms. Ceftriaxone is resistant to the ratio of beta-lactamase enzymes (both penicillinase and cephalosporinase, produced by the majority of gram-positive and gram-negative bacteria). Effective against the following microorganisms:

    Gram-positive

    Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, Streptococcus A (Str.pyogenes), Streptococcus V (Str. agalactiae), Streptococcus viridans, Streptococcus bovis. Note: Staphylococcus spp., resistant to methicillin, is resistant to cephalosporins, including ceftriaxone. Most strains of enterococci (for example, Streptococcus faecalis) also resistant to ceftriaxone.

    Gram-negative

    Aeromonas spp., Alcaligenes spp., Branhamella catarrhalis, Citrobacter spp., Enterobacter spp. (some strains are stable), Escherichia coli, Haemophilus ducreyi, Haemophilus influenzae, Haemophilus parainfluenzae, Klebsiella spp. (at Tom number of Kl. pneumoniae), Moraxella spp., Morganella morganii, Neisseria gonorrhoeae, Neisseria meningitidis, Plesiomonas shigelloides, Proteus mirabilis, Proteus vulgaris, Providencia spp., Pseudomonas aeruginosa (some strains are stable), Salmonella spp. (at Tom number of S. typhi), Serratia spp. (at Tom number of S. marcescens), Shigella spp., Vibrio spp. (at Tom number of V. cholerae), Yersinia spp. (at Tom number of Y. enterocolitica)

    Note: many strains of these microorganisms, which in the presence of other antibiotics, for example, penicillins, first-generation cephalosporins and aminoglycosides, are multiplying steadily, are sensitive to ceftriaxone. Treponema pallidum is sensitive to ceftriaxone as in vitro, and in experiments on animals. According to clinical data, in the primary and secondary syphilis, a good efficacy of ceftriaxone is noted.

    Anaerobic pathogens

    Bacteroides spp. (including some strains of B. fragilis), Clostridium spp. (at Tom number of FROM1. difficile), Fusobacterium spp. (Besides F. mostiferum. F. varium), Peptococcus spp., Peptostreptococcus spp.

    Note: some strains of many Bacteroides spp. (for example, in. fragilis), Developing beta-lactamase, resistant to ceftriaxone. To determine the sensitivity of microorganisms, discs containing ceftriaxone, since it is shown that in vitro to classical cephalosporins, certain strains of pathogens can be stable.

    Pharmacokinetics:
    With parenteral administration ceftriaxone well penetrates into tissues and body fluids. In healthy adults, the subjects for ceftriaxone are characterized by a long half-life period of about 8 hours. The area under the concentration curve - time in the blood serum for intravenous and intramuscular injection coincide. This means that the bioavailability of ceftriaxone when administered intramuscularly is 100%. With intravenous administration ceftriaxone quickly diffuses into the interstitial fluid, where its bactericidal action against pathogens sensitive to it persists for 24 hours. Ceftriaxone reversibly binds to albumin and this binding is inversely proportional to the concentration: for example, when the concentration of the drug in the serum is less than 100 mg / l, the binding of ceftriaxone to proteins is 95%, and at a concentration of 300 mg / l, only 85%. Due to the lower content of albumins in the interstitial fluid, the concentration of ceftriaxone in it is higher than in serum.
    The half-life in healthy adults is about 8 hours. In newborns up to 8 days and in elderly people older than 75 years, the average half-life is approximately twice as large. In adults, 50-60% of ceftriaxone is excreted unchanged in urine, and 40-50% is also unchanged in bile. Under the influence of intestinal flora ceftriaxone turns into an inactive metabolite. In neonates, approximately 70% of the administered dose is excreted by the kidneys. In renal failure or liver disease in adults pharmacokinetics ceftriaxone hardly changes, half-life period is lengthened slightly. If the kidney function is impaired, the secretion with bile increases, and if liver pathology takes place, then the excretion of ceftriaxone by the kidneys increases.
    Penetration into the cerebrospinal fluid: in newborns and in children with inflammation of the meninges ceftriaxone penetrates into the cerebrospinal fluid, while in the case of bacterial meningitis, an average of 17% of the concentration of the drug in the blood serum diffuses into the cerebrospinal fluid, which is approximately 4 times greater than with aseptic meningitis. 24 hours after intravenous administration of ceftriaxone in a dose of 50-100 mg / kg body weight, the concentration in the cerebrospinal fluid exceeds 1.4 mg / L.In adults with meningitis, 2 to 25 hours after the administration of ceftriaxone at a dose of 50 mg / kg body weight, the concentration of ceftriaxone was many times greater than the minimum oppressive dose that is necessary to suppress the pathogens most commonly causing meningitis.
    Indications:
    Infections caused by susceptible to ceftriaxone pathogens: sepsis, meningitis, infections of the abdominal cavity (peritonitis, inflammatory diseases of the gastrointestinal tract, bile ducts), infections of bones, joints, connective tissue, skin, infection in patients with low immunity, infection of the kidneys and urinary tract pathways, respiratory tract infections (including pneumonia), as well as infections of LOP-organs, urogenital infections (including gonorrhea). Prevention of infections in the postoperative period.
    Contraindications:Hypersensitivity to cephalosporins, penicillins and carbapenems. The first trimester of pregnancy.
    Carefully:Hyperbilirubinemia in newborns, premature infants, renal / hepatic insufficiency, ulcerative colitis, enteritis or colitis associated with the use of antibacterial drugs, pregnancy 2-3 trimester, lactation.
    Dosing and Administration:

    For adults and for children over 12 years old

    The average daily dose is 1-2 g of ceftriaxone once a day or 0.5-1 g every 12 hours. In severe cases or in cases of infections caused by moderately sensitive pathogens, the daily dose can be increased to 4 g.

    For newborns

    For a single daily dosage, the following scheme is recommended:

    For newborns (up to 2 weeks of age): 20-50 mg / kg of body weight per day (a dose of 50 mg / kg of body weight is not recommended because of the immature enzyme system of newborns).

    For infants and children under 12 years of age The daily dose is 20-75 mg / kg body weight.

    Children with a body weight of 50 kg and above should adhere to the dosage for adults. Dose more

    50 mg / kg body weight should be administered as an intravenous infusion, at least in

    for 30 minutes.

    Duration of therapy

    Depends on the course of the disease.

    Meningitis

    In bacterial meningitis in newborns and in children, the initial dose is 100 mg / kg of body weight once a day (maximum 4 g). Once it was possible to isolate the pathogenic microorganism and determine its sensitivity, the dose should be reduced accordingly.

    Causative agent

    Duration of therapy

    Neisseria meningitidis

    4 days

    Haemophilus influenzae

    6 days

    Streptococcus pneumoniae

    7 days

    Sensitive Enterobacteriacease

    10-14 days

    Gonorrhea

    For the treatment of gonorrhea caused by both generative and non-penicillinase-resistant strains, the recommended dose is 250 mg once intramuscularly.

    Prevention in the pre- and postoperative period

    Before infected or suspected infected surgical interventions to prevent postoperative infections, depending on the risk of infection, one-time administration of ceftriaxone in a dose of 1-2 g is recommended 30-90 minutes prior to surgery.

    Lack of kidney and liver function

    In patients with impaired renal function, under the condition of normal liver function, a dose of ceftriaxone is not necessary to reduce. Only if the kidneys are deficient in the preterminal stage (creatinine clearance below 10 ml / min) it is necessary that the daily dose of ceftriaxone does not exceed 2 g.

    In patients with impaired liver function, if the function of the kidneys is maintained, the dose of ceftriaxone should not be reduced.

    In cases of simultaneous presence of severe pathology of the liver and kidneys, the concentration of ceftriaxone in serum should be monitored regularly.In patients undergoing hemodialysis, the dose of the drug after this procedure is not necessary to change.

    Intramuscular injection

    For intramuscular injection, 1 g of the drug should be diluted in 3.5 ml of a 1% solution of lidocaine and inserted deep into the gluteal muscle, it is recommended to inject no more than 1 g of the drug into one buttock. A solution of lidocaine can never be administered intravenously! Intravenous administration

    For intravenous injection, 1 g of the drug should be diluted in 10 ml of sterile distilled water and administered intravenously slowly for 2-4 minutes.

    Intravenous infusion

    Duration of intravenous infusion is at least 30 minutes. For intravenous infusion, 2 g of the drug should be diluted in approximately 40 ml of a calcium free solution, for example: in a 0.9% solution of sodium chloride, in a 5% solution of dextrose, in a 10% solution of dextrose, 5% solution of fructose.

    Side effects:
    Allergic reactions: urticaria, chills or fever, rash, itching, rarely - bronchospasm, eosinophilia, erythema, polymorphic exudative (including Stevens-Johnson syndrome), serum sickness, angioedema, anaphylactic shock.
    From the side of the digestive system: nausea, vomiting, diarrhea or constipation, flatulence, abdominal pain, taste disorder, stomatitis, glossitis, pseudomembranous enterocolitis, impaired liver function (increased activity of "liver" transaminases, less often - alkaline phosphatase or bilirubin, cholestatic jaundice), pseudocholithiasis gall bladder ("sludge" - a syndrome), a dysbacteriosis.
    On the part of the hematopoiesis: leukopenia, leukocytosis, neutropenia, granulocytopenia, lymphopenia, thrombocytosis, thrombocytopenia, hemolytic anemia, basophilia, hypocoagulation, decrease in plasma clotting factor concentration (II, VII, IX, X), prolongation of prothrombin time.
    On the part of the urinary system: renal dysfunction (azotemia, increased urea in the blood, hypercreatininaemia, glycosuria, cylindruria, hematuria), oliguria, anuria.
    Local reactions: phlebitis, pain along the vein, soreness and infiltration at the site of the / m introduction.
    Other: headache, dizziness, nosebleeds, candidiasis, superinfection.
    Overdose:Excessively high concentrations of ceftriaxone in plasma can not be reduced by hemodialysis or peritonealdialysis. Symptomatic measures are recommended for the treatment of overdose cases.
    Interaction:
    Ceftriaxone and aminoglycosides have a synergistic effect on many Gram-negative bacteria.
    Incompatible with ethanol.
    Nonsteroidal anti-inflammatory drugs and other inhibitors of platelet aggregation increase the likelihood of bleeding.
    With simultaneous use with "loop" diuretics and other nephrotoxic drugs, the risk of developing nephrotoxic action increases. Pharmaceutically incompatible with solutions containing other antibiotics.
    Special instructions:
    With simultaneous severe renal and hepatic insufficiency, the concentration of the drug in the plasma should be regularly determined.
    In patients who are on hemodialysis, it is necessary to monitor the concentration of ceftriaxone in the plasma, tk. they can decrease the rate of its excretion.
    With long-term treatment, it is necessary to regularly monitor the picture of peripheral blood, indicators of the functional state of the liver and kidneys.
    In rare cases, with ultrasound of the gallbladder, blackouts are noted, which disappear after cancellation (even if this phenomenon is accompanied by pain in the right hypochondrium,recommend continued use of antibiotic and symptomatic treatment).
    During treatment, the use of ethanol is contraindicated - disulfiramoid-like effects are possible (red face, spasm in the stomach, nausea, vomiting, headache, lowering blood pressure, tachycardia, dyspnea).
    Despite the detailed history, which is the rule for other cephalosporin antibiotics, one can not exclude the possibility of developing an anaphylactic shock that requires immediate therapy - first intravenously injected epinephrine, then glucocorticoids. In vitro studies have shown that, like other cephalosporin antibiotics ceftriaxone is able to displace bilirubin, associated with serum albumin. Therefore, in newborns with hyperbilirubinemia and, especially, in preterm infants, the use of ceftriaxone requires even greater caution. When appointing during lactation, it is necessary to cancel breastfeeding. Elderly and debilitated patients may require the appointment of vitamin K.

    Form release / dosage:Powder for the preparation of solution for intramuscular and intravenous administration of 0.25 g, 0.5 g and 1 g.
    Packaging:Powder for preparation of solution for intramuscular and intravenous administration of 0.25 g, 0.5 g and 1 g of ceftriaxone, in colorless glass bottles, type I, sealed with rubber stoppers and crimped with aluminum caps with plastic caps; 1 bottle per carton, along with instructions for medical use.
    Storage conditions:At a temperature of no higher than 25 ° C. Keep out of the reach of children.
    Shelf life:2 years. Do not use after the expiration date.
    Terms of leave from pharmacies:On prescription
    Registration number:LSR-003634/10
    Date of registration:30.04.2010
    The owner of the registration certificate:Shraya Life Senses Pvt. Ltd.Shraya Life Senses Pvt. Ltd. India
    Manufacturer: & nbsp
    Representation: & nbspSHREYA LIFE SENENSIZ Pvt.Ltd. SHREYA LIFE SENENSIZ Pvt.Ltd. India
    Information update date: & nbsp21.11.2015
    Illustrated instructions
      Instructions
      Up