Active substancePiperacillin + TazobactamPiperacillin + Tazobactam
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  • Dosage form: & nbspPowder for solution for intravenous administration.
    Composition:1 bottle contains:
    Active substances:
    Piperacillin sodium is equivalent to piperacillin 4000.00 mg
    Tazobactam sodium is equivalent to tazobactam 500.00 mg

    Description:White or almost white powder.

    Pharmacotherapeutic group:Antibiotic-penicillin semisynthetic + beta-lactamase inhibitor.
    ATX: & nbsp

    J.01.C.R.05   Piperacillin in combination with enzyme inhibitors

    Pharmacodynamics:Piperacillin is a semisynthetic bactericidal broad-spectrum antibiotic that is active against many Gram-positive and Gram-negative aerobic and anaerobic bacteria. Piperacillin inhibits the synthesis of the membrane of the cell wall of the microorganism. Tazobactam is a sulfonic derivative of triazolmethylpenicillic acid, a potent inhibitor of many beta-lactamases (including plasmid and chromosomal beta-lactamases), which often cause resistance to penicillins and cephalosporins, including third-generation cephalosporins. The presence of tazobactam in the combination drug enhances antimicrobial activity and expands
    spectrum of the action of piperacillin due to the inclusion of bacteria forming beta-lactamases, which are usually resistant to piperacillin and other beta-lactam antibiotics. The drug is active against:
    Gram-negative bacteria: producing and non-producing beta-lactamase strains Escherichia coli, Citrobacter spp. (including Citrobacter freundii, Citrobacter diversus), Klebsiella spp. (including Klebsiella oxytoca, Klebsiella pneumoniae), Enterobacter spp. (including Enterobacter cloaca, Enterobacter aerogenes), Proteus vulgaris, Proteus mirabilis, Providencia rettgery, Providencia stuartii, Plesiomonas shigelloides, Morganella morganii, Serratia spp. (including Serratia marcescens, Serratia liquifaciens), Salmonella spp., Shigella spp., Pseudomonas aeruginosa and others Pseudomonas spp. (including Pseudomonas cepacia, Pseudomonas fluorescens), Xanthamonas maltophilia, Neisseria gonorrhoeae, Neisseria meningitidis, Moraxella spp. (including Branhamella catarrhalis), Acinetobacter spp., Haemophilus influenzae, Haemophilus parainfluenza, Pasteurella multocida, Yersinia spp., Campylobacter spp., Gardnerella vaginalis.
    Gram-positive bacteria: producing and non-producing beta-lactamase strains Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes, Streptococcus bovis, Streptococcus, agalactiae. Streptococcus spp. groups viridans subgroups (C and G), Enterococcus spp. (Enterococcus faecalis, Enterococcus faecium), Staphylococcus aureus (sensitive to methicillin), Staphylococcus saprophyticus, Staphylococcus epidermidis (coagulase negative), Listeria monocytogenes, Nocardia spp.
    Anaerobic bacteria: producing and non-producing beta-lactamase strains Bacteroides spp. (Bacteroides bivius, Bacteroides disiens, Bacteroides capillosus, Bacteroides melaninogenicus, Bacteroides oralis), subgroups Bacteroides fragilis (Bacteroides fragilis, Bacteroides fragilis, Bacteroides fragilis, Bacteroides distasonis, Bacteroides ovatus, Bacteroides thetaiotaomicron, Bacteroides uniformis, Bacteroides asaccharolyticus), Peptostreptococcus spp., Fusobacterium spp., Eubacterium spp., Clostridium spp. (including Clostridium difficile, Clostridium perfringens), Veilonella spp. and Actynomyces spp.

    Pharmacokinetics:The maximum concentrations of piperacillin and tazobactam in plasma are reached immediately after completion of intravenous administration.
    When the dose of the combination is increased piperacillin 2 g / tazobactam 250 mg to 4 g / 500 mg, respectively, a disproportionate increase (approximately 28%) of the concentration of piperacillin and tazobactam.
    The connection with the plasma proteins of both piperacillin and tazobactam is approximately 30%, with the presence of tazobactam not affecting this parameter of piperacillin, and the presence of piperacillin - tazobactam.
    Piperacillin and tazobactam are widely distributed in tissues and body fluids, including in the intestinal mucosa, gall bladder, lungs, bile, female genitalia (uterus, ovaries and fallopian tubes) and bones.The average concentrations in tissues are from 50 to 100% of the concentration in the plasma.
    Piperacillin is metabolized to a low-activity deshetylmetabolite; tazobactam - to an inactive metabolite. Piperacillin and tazobactam are excreted by the kidneys through glomerular filtration and canaliculia secretion. Piperacillin is rapidly excreted unchanged, 68% of the administered dose is found in the urine. Tazobactam and its metabolite are rapidly excreted by renal excretion, 80% of the dose taken is unchanged, and the remaining amount is in the form of a metabolite. Piperacillin, tazobactam and desethylpiperacillin are also excreted with bile and excreted by the intestine.
    The half-life (Tl / 2) of piperacillin and tazobactam from the plasma is approximately 0.7-1.2 hours. With a decrease in the creatinine clearance of T1 / 2, piperacillin and tazobactam are elongated.
    Impaired renal function
    As the creatinine clearance (KK) T1 / 2 decreases, piperacillin and tazobactam increase. With a decrease in KK of less than 20 ml / min, T1 / 2 of piperacillin and tazobactam, compared with patients with normal renal function, increase 2 and 4 times, respectively.
    During hemodialysis, 30 to 50% of piperacillin and 5% of the dose of tazobactam in the form of a metabolite are excreted. When peritoneal dialysis is performed, respectively, about 6 and 21% of piperacillin and tazobactam, with 18% of the tazobactam excreted as its metabolite.
    Impaired liver function
    Although in patients with a violation of liver function T1 / 2 piperazillina and tazobactam increase, dose adjustment is not required.



    Indications:Infectious-inflammatory diseases caused by microorganisms sensitive to piperacillin / tazobactam.

    Adults and children over 12 years of age:
    - Lower respiratory tract infections;
    - Urinary tract infections (complicated and uncomplicated);
    - Intraabdominal infections;
    - Infections of the skin and soft tissues;
    - Septicemia;
    - Gynecological infections (including endometritis and adnexitis in the postpartum period);
    - Bacterial infections in patients with neutropenia (in combination with aminoglycosides);
    - Infections of bones and joints;
    - Mixed infections (caused by Gram-positive / Gram-negative aerobic and anaerobic microorganisms).
    Children between the ages of 2 and 12:
    - Intraabdominal infections;
    - Infections against neutropenia (in combination with aminoglycosides).


    Contraindications:Hypersensitivity to beta-lactam antibiotics (including penicillins, cephalosporins), other components of the drug or to beta-lactamase inhibitors. Children under 2 years.

    Carefully:Severe bleeding (including history), cystic fibrosis (increased risk of hyperthermia and skin rash), pseudomembranous colitis, children over 2 years of age, renal failure (CC less than 20 ml / min), patients on hemodialysis, with joint application of high doses of anticoagulants, with hypokalemia.

    Pregnancy and lactation:There is insufficient data on the use of a combination of piperacillin / tazobactam in pregnant women. Piperacillin and tazobactam penetrate the placental barrier. Pregnant women drug can be prescribed only in those cases when the expected benefit for the mother exceeds the possible risk to the fetus.
    Piperacillin in low concentrations is secreted with breast milk; the isolation of tazobactam in milk has not been studied. If it is necessary to use the drug during lactation, it is necessary to stop breastfeeding during the treatment.




    Dosing and Administration:Intravenously slowly run for at least 3-5 minutes or drip for 20-30 minutes.
    The duration of treatment is determined by the severity of the infectious process and the dynamics of clinical and bacteriological indicators.
    Adults and children over 12 years with normal renal function
    The recommended dose of the drug, which is prescribed every 8 hours, is 4.5 g (4 g piperacillin / 0.5 g tazobactam).
    The total daily dose depends on the severity and localization of the infection and can vary from 2.25 g (2 g piperacillin / 0.25 g tazobactam) to 4.5 g (4 g piperacillin / 0.5 g tazobactam) drug administered every 6 or 8 hours
    Children aged from 2 to 12 years.
    For neutropenia:
    In patients with normal kidney function and body weight less than 50 kg with a fever resulting from neutropenia, the dose is 90 mg (80 mg piperacillin / 10 mg tazobactam) per kilogram of body weight, which is injected every 6 hours in combination with the appropriate dose aminoglycoside.
    In children with a body weight of more than 50 kg, the dose corresponds to an adult, and is administered in combination with aminoglycosides.
    With intra-abdominal infection: In children with a body weight of up to 40 kg and normal renal function, the recommended dose is 112.5 mg / kg (100 mg piperacillin / 12.5 mg tazobactam) every 8 hours.
    Children with a body weight of more than 40 kg and normal kidney function are given the same dose as an adult, i.e. 4.5 g of the drug (4 g piperacillin / 0.5 g tazobactam) every 8 hours. Treatment should be at least 5 days and no more than 14 days, given that the drug is continued for at least 48 more h after the disappearance of clinical signs of infection.
    Impaired renal function
    Patients with renal insufficiency or a patient on hemodialysis, dose and frequency of administration should be adjusted for the degree of impaired renal function.
    Recommended doses of the drug for adults and children (body weight> 50 kg) with renal failure

    (creatine kinase) (ml / min)

    Recommended dosage of piperacillin / tazobactam

    >40

    Dose correction is not required

    20-40

    12 g / 1,5 g / day (4 g / 0.5 g every 8 h)

    <20

    8 g / 1 g / day (4 g / 0.5 g every 12 hours)

    For patients on hemodialysis, the maximum daily dose is 8 g / 1 g of piperacillin / tazobactam. In addition, since 30-50% piperacillin is withdrawn from the hemodialysis within 4 hours, one additional dose of 2 g / 0.25 g piperacillin / tazobactam should be given after each dialysis session.
    Children 2-12 years with renal insufficiency:
    The pharmacokinetics of piperacillin / tazobactam in children with renal insufficiency have not been studied. For children aged 2-12 years with renal insufficiency, it is recommended to adjust the dose as follows:
    Recommended doses of the drug for children (body weight <50 kg) with renal failure

    Creatinine clearance

    The dose of piperacillin / tazobactam

    >50 ml / min

    112,5 mg / kg (100 mg piperacillin /12,5 mg tazobactam) every 8 h

    < 50 ml / min

    78,75 mg / kg (70 mg piperacillin / 8,75 mg tazobactam) every 8 h

    Such a change in dose is only indicative. Each patient should be monitored for the timely detection of signs of an overdose. It is necessary to adjust the dose of the drug and the interval between the administration of the next dose accordingly.
    No dosage adjustment required with a violation of the liver.
    In elderly patients, dose adjustment is necessary only if there is a violation of kidney function.
    Method of solution preparation.
    The preparation is dissolved in one of the following solvents in accordance with the indicated volumes. The vial is rotated in a circular motion until the content is completely dissolved (with constant rotation, usually for 5-10 min).The prepared solution is a colorless or pale yellow liquid.

    Dosage / vial (piperacillin / tazobactam)

    Required volume of solvent

    4.50 g (4 g / 500 mg)

    20 ml

    Solvents compatible with the preparation: 0.9% solution of sodium chloride; sterile water for injections; 5% dextrose solution.
    Then the prepared solution can be diluted to the volume required for intravenous administration (for example, from 50 ml to 150 ml) by one of the following compatible solvents: 0.9% sodium chloride solution; sterile water for injections (the maximum recommended volume is 50 ml); 5% dextrose solution.

    Side effects:Allergic reactions: urticaria, skin itch, rash, bullous dermatitis, erythema multiforme Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylactic / anaphylactoid reactions (including anaphylactic shock). On the part of the digestive system: diarrhea, nausea, vomiting, constipation, dyspepsia, jaundice, stomatitis, abdominal pain, pseudomembranous colitis, hepatitis.
    On the part of the organs of hematopoiesis: leukopenia, neutropenia, thrombocytopenia, anemia, bleeding (including purpura, nosebleeds,increased bleeding time), hemolytic anemia, agranulocytosis, false-positive direct Coombs test, pancytopenia, increased activated partial thromboplastin time, increased prothrombin time, thrombocytosis.
    From the urinary system: interstitial nephritis, kidney failure.
    From the nervous system: headache, insomnia, cramps.
    From the cardiovascular system: lowering blood pressure, "hot flashes".
    Laboratory indicators: hypoalbuminemia, hypoglycemia, hypoproteinemia, hypokalemia, eosinophilia, increased activity of "hepatic" transaminases (alanine aminotransferase, aspartate aminotransferase), hyperbilirubinemia, increased activity of alkaline phosphatase, gamma-glutamyltransferase, increased serum creatinine and urea concentration.
    Local reactions: phlebitis, thrombophlebitis, hyperthermia at the injection site, hyperemia and compaction at the site of administration.
    Other: fungal superinfections, fever, arthralgia.

    Overdose:Symptoms: nausea, vomiting, diarrhea, increased neuromuscular excitability and convulsions.
    Treatment: depending on the clinical manifestations, symptomatic treatment is prescribed. To reduce high concentrations of piperacillin or tazobactam in the serum, hemodialysis can be prescribed.

    Interaction:The combined use of the drug with probenecid increases T1 / 2 and decreases the renal clearance of both piperacillin and tazobactam, but the maximum plasma concentrations of both drugs remain unchanged.

    The simultaneous use of the drug and vecuronium bromide can lead to a longer neuromuscular blockade caused by the latter (a similar effect can be observed with a combination of piperacillin with other nondepolarizing muscle relaxants).
    With the simultaneous use of high doses of heparin, indirect anticoagulants or other drugs that affect the blood clotting system, including the function of platelets, it is necessary to more often monitor the state of the blood coagulation system. Piperacillin may delay the excretion of methotrexate (in order to avoid a toxic effect it is necessary to monitor the concentration of methotrexate in the blood serum).
    Pharmaceutical compatibility with other drugs
    The drug should not be mixed in one syringe or dropper with other medicines, including. with aminoglycosides. When used in conjunction with other antibiotics, drugs should be administered separately; most preferably the administration of piperacillin / tazobactam and aminoglycoside is delineated in time.
    The drug should not be used in conjunction with solutions containing sodium hydrogen carbonate and add to blood products or albumin hydrolysates.

    Special instructions:Before starting treatment, the patient should be interviewed in detail to identify possible reactions of hypersensitivity to penicillins, cephalosporins or other allergens. Severe allergic reactions are more likely to develop in patients with increased sensitivity to several allergens. Such reactions require discontinuation of the drug and the introduction of epinephrine (Adrenaline) and other emergency measures.
    The pseudomembranous colitis caused by antibiotics can be manifested by severe, persistent diarrhea, which poses a threat to life. Pseudomembranous colitis can develop both during antibiotic therapy and after its completion.In such cases, the drug should be discontinued immediately and appropriate therapy should be prescribed (eg, by mouth metronidazole, vancomycin). Preparations that inhibit intestinal motility are contraindicated.
    In the treatment, especially long-term, the development of leukopenia and neutropenia, so you need to periodically monitor the peripheral blood.
    In a number of cases (most often in patients with renal insufficiency), the appearance of increased bleeding and concomitant changes in the laboratory parameters of the blood coagulation system (clotting time, platelet aggregation and prothrombin time) is likely. If bleeding occurs, discontinue treatment with the drug and prescribe appropriate therapy.
    It should be borne in mind the possibility of the emergence of resistant microorganisms, which can cause, superinfection, especially with a long course of treatment. This preparation contains 2.79 mEq. (64 mg) of sodium per gram of piperacillin, which can lead to a general increase in sodium intake. In patients with hypokalemia or taking drugs that promote the excretion of potassium,during the treatment may develop hypokalemia (it is necessary to regularly check the content of electrolytes in the blood serum).
    No experience in children under 2 years of age.
    During the use of the drug, a false positive result can be obtained for glucose in the urine using a method based on the reduction of copper ions. Therefore, it is recommended to carry out a test based on enzymatic oxidation of glucose (glucose oxidase method).

    Effect on the ability to drive transp. cf. and fur:Given the possibility of developing side effects from the CNS in the treatment of the drug, care should be taken when working with mechanisms and driving vehicles.
    Form release / dosage:Powder for the preparation of a solution for intravenous administration of 4 g + 0.5 g.
    Packaging:For 4 g of piperacillin and 0.5 g of tazobactam in a vial of colorless glass, corked with a cork of gray chlorobutyl rubber, coated with an aluminum cap. 1 bottle with instructions for use in a cardboard box.
    By 5, 10 or 50 bottles with an equal number of instructions for use in a cardboard box (for hospitals).

    Storage conditions:In the dark place 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 printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:LP-001784
    Date of registration:24.07.2012
    The owner of the registration certificate:ARS, LLC ARS, LLC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp24.07.2012
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