Active substanceAmoxicillin + Clavulanic acidAmoxicillin + Clavulanic acid
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  • Dosage form: & nbspfilm coated tablets
    Composition:

    Composition of the preparation (per 1 tablet)

    Active substances:

    Amoxicillin trihydrate in terms of amoxicillin 875.0 mg.

    Potassium clavulanate in terms of clavulanic acid 125.0 mg.

    Excipients:

    tablet core: magnesium stearate, sodium carboxymethyl starch, silicon colloidal dioxide, microcrystalline cellulose;

    film membrane tablets: titanium dioxide, hypromellose (5 cP), hypromellose (15 cP), macrogol-4000, macrogol-6000, dimethicone.

    Ratio of active components

    Dosage form

    Ratio of active

    components

    Amoxicillin, mg (in the form of amoxicillin trihydrate)

    Clavulanic acid, mg (in the form of potassium clavulanate)

    Tablets 875 mg / 125 mg

    7:1

    875

    125

    Description:The film-coated tablets are oval in shape from white to almost white with letters A and C on both sides of the tablets and a line of fracture on one side of the tablet. Tablets from yellowish white to almost white in color at the break.
    Pharmacotherapeutic group:Antibiotic - penicillin semisynthetic + beta-lactamase inhibitor
    ATX: & nbsp

    J.01.C.R.02   Amoxicillin in combination with enzyme inhibitors

    Pharmacodynamics:

    Mechanism of action

    Amoxicillin is a semisynthetic broad-spectrum antibiotic with activity against many Gram-positive and Gram-negative microorganisms. In the same time amoxicillin is subject to destruction by beta-lactamases, and therefore the spectrum of amoxicillin activity does not extend to microorganisms that produce this enzyme.

    Clavulanic acid, a beta-lactamase inhibitor structurally related to penicillins, has the ability to inactivate a wide spectrum of beta-lactamases found in microorganisms resistant to penicillins and cephalosporins. Clavulanic acid has sufficient efficacy against plasmid beta-lactamases, which most often cause bacterial resistance, and is not effective against type 1 chromosomal beta lactamases that are not inhibited by clavulanic acid.

    The presence of clavulanic acid in the preparation of Augmentin ® protects amoxicillin from destruction by enzymes - beta-lactamases, which allows to expand the antibacterial spectrum of amoxicillin.

    The activity of a combination of amoxicillin with clavulanic acid in vitro is given below.

    Bacteria, usually sensitive to a combination of amoxicillin and clavulanic acid

    Gram-positive aerobes

    Bacillus anthracis

    Enterococcus faecalis

    Listeria monocytogenes

    Nocardia asteroides

    Streptococcus pyogenes1,2

    Streptococcus agalactiae1,2

    Streptococcus spp. (other beta-hemolytic streptococci)1,2

    Staphylococcus aureus (sensitive to methicillin)1

    Staphylococcus saprophyticus (sensitive to methicillin)

    Coagulase-negative staphylococci (sensitive to methicillin)

    Gram-positive anaerobes

    Clostridium spp.

    Peptococcus niger

    Peptostreptococcus magnus

    Peptostreptococcus micros

    Peptostreptococcus spp.

    Gram-negative aerobes

    Bordetella pertussis

    Haemophilus influenzae1

    Helicobacter pylori

    Moraxella catarrhalis1

    Neisseria gonorrhoeae

    Pasteurella multocida

    Vibrio cholerae

    Gram-negative anaerobes

    Bacteroides fragilis

    Bacteroides spp.

    Capnocytophaga spp.

    Eikenella corrodens

    Fusobacterium nucleatum

    Fusobacterium spp.

    Porphyromonas spp.

    Prevotella spp.

    Other

    Borrelia burgdorferi

    Leptospira icterohaemorrhagiae

    Treponema pallidum

    Bacteria for which the acquired resistance to a combination of amoxicillin and clavulanic acid is probable

    Gram-negative aerobes

    Escherichia coli1

    Klebsiella oxytoca

    Klebsiella pneumoniae1

    Klebsiella spp.

    Proteus mirabilis

    Proteus vulgaris

    Proteus spp.

    Salmonella spp.

    Shigella spp.

    Gram-positive aerobes

    Coiynebacterium spp.

    Enterococcus faecium

    Streptococcus pneumoniae1,2

    Streptococcus group Viridans

    Bacteria that have natural resistance to a combination of amoxicillin and clavulanic acid

    Gram-negative aerobes

    Acinetobacter spp.

    Citrobacterfreundii

    Enterobacter spp.

    Hafnia alvei

    Legionella pneumophila

    Morganella morganii

    Providencia spp.

    Pseudomonas spp.

    Serratia spp.

    Stenotrophomonas maltophilia

    Yersinia enterocolitica

    Other

    Chlamydia pneumoniae

    Chlamydia psittaci Chlamydia spp. Coxiella burnetii

    Mycoplasma spp.

    1 - for these bacteria, the clinical efficacy of a combination of amoxicillin with clavulanic acid has been demonstrated in clinical studies.

    2 - strains of these bacteria do not produce beta-lactamases.

    Sensitivity to monotherapy with amoxicillin suggests a similar sensitivity to the combination of amoxicillin and clavulanic acid.

    Pharmacokinetics:

    Suction

    Both active substances drug Augmentin®, amoxicillin and clavulanic acid, are quickly and completely absorbed from the gastrointestinal tract (GIT) after oral administration. Absorption of active substances of the drug Augmentin® is optimal in case of taking the drug at the beginning of food intake.

    Below is the data pharmacokinetic parameters amoxicillin and clavulanic acid, obtained in separate studies, when healthy volunteers on an empty stomach accepted:

    2 tablets of the drug Augmentin®, 875 mg / 125 mg (1000 mg).

    Basic pharmacokinetic parameters

    A drug

    Dose

    (mg)

    Cmax

    (mg / ml)

    Tmax

    (hours)

    s)

    AUC

    (mg * h /

    ml)

    T1/2

    (clock)

    Amoxicillin in the drug Augmentin®

    Augmentin®, 875 mg / 125 mg

    1750

    11,64 ± 2,78

    1,50

    (1,0-

    2,5)

    53,52 ± 12,31

    1,19 ± 0,21

    Clavulanic acid as a part of the preparation of Augmenty®

    Augmentin®, 875 mg / 125 mg

    250

    2,18 ± 0,99

    1,25

    (1,0-

    2,0)

    10,16 ± 3,04

    0,96 ± 0,12

    Cmax- maximum concentration in blood plasma.

    Tmax - time to reach the maximum concentration in the blood plasma.

    AUC- the area under the concentration-time curve.

    T1/2 - half-life.

    Distribution

    As with intravenous combination of amoxicillin with clavulanic acid, therapeutic concentrations of amoxicillin and clavulanic acid are found in various tissues and interstitial fluid (in the gall bladder, abdominal tissues, skin, fat and muscle tissues, synovial and peritoneal fluids, bile secretion) .

    Amoxicillin and clavulanic acid have a weak degree of binding to plasma proteins. The conducted studies showed that about 25% of the blood plasma proteins bind, total clavulanic acid and 18% amoxicillin in blood plasma.

    In animal studies, no cumulation of components of the Augmentin® preparation in any organ was detected. Amoxicillin, like most penicillins, penetrates into breast milk. Traces of clavulanic acid can also be detected in breast milk. With the exception of the possibility of developing sensitization, diarrhea or candidiasis of the oral mucosa, there are no known other negative effects of amoxicillin and clavulanic acid on the health of infants fed by breast milk.

    Studies of reproductive function in animals have shown that amoxicillin and clavulanic acid penetrate the placental barrier. However, there was no adverse effect on the fetus.

    Metabolism

    10-25% of the initial dose of amoxicillin is excreted by the kidneys in the form of an inactive metabolite (penicillic acid). Clavulanic acid undergoes intensive metabolism to 2,5-dihydro-4- (2-hydroxyethyl) -5-oxo-1 H-pyrrole-3-carboxylic acid and 1-amino-4-hydroxybutan-2-one and is excreted by the kidneys , through the gastrointestinal tract, and also with exhaled air in the form of carbon dioxide.

    Excretion

    Like other penicillins, amoxicillin is excreted mainly by the kidneys, whereas clavulanic acid - through both renal and extrarenal mechanisms.

    Approximately 60-70% of amoxicillin and about 40-65% of clavulanic acid is excreted by the kidneys unchanged in the first 6 hours after the administration of the drug. Simultaneous administration of probenecid slows the excretion of amoxicillin, but not clavulanic acid (see section "Interaction with other drugs").

    Indications:

    Bacterial infections caused by microorganisms sensitive to amoxicillin-clavulanic acid:

    - ENT organs infections, eg, relapsing tonsillitis, sinusitis, otitis media, usually caused by Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis and Streptococcus pyogenes.

    - Infections of the lower respiratory tract, for example, exacerbations of chronic bronchitis, lobar pneumonia and bronchopneumonia, commonly caused by Streptococcus pneumoniae, Haemophilus influenzae and Moraxella catarrhalis.

    - Urinary tract infections, such as cystitis, urethritis, pyelonephritis, infections of the female genitalia, usually caused by species of the Enterobacteriaceae family (mainly Escherichia coli), Staphylococcus saprophyticus and species of the genus Enterococcus, and gonorrhea caused by Neisseria gonorrhoeae.

    - Infections of the skin and soft tissues, usually caused by Staphylococcus aureus, Streptococcus pyogenes and species of the genus Bacteroides.

    - Infections of bones and joints, for example osteomyelitis, usually caused by Staphylococcus aureus, if long-term therapy is necessary.

    - Other mixed infections (eg septic abortion, obstetric sepsis, intra-abdominal sepsis) in the framework of stepwise therapy.

    Infections caused by microorganisms sensitive to amoxicillin can be treated with the drug "Augmentin®" because amoxicillin is one of its active ingredients.

    Contraindications:

    - Hypersensitivity to beta-lactams, for example to penicillins and cephalosporins or other components of the drug;

    - previous episodes of jaundice or impaired liver function with amoxicillin / clavulanic acid in history;

    - Children under 12 years of age (for this dosage form);

    - impaired renal function (creatinine clearance less than or equal to 30 ml / min).

    Carefully:

    Violation of the function of the liver.

    Pregnancy and lactation:

    Pregnancy

    In studies of reproductive function in animals, oral and parenteral administration of the Augmentin® drug did not produce teratogenic effects. In a single study in women with premature rupture of membranes, it was found that preventive therapy with the drug may be associated with an increased risk of developing necrotizing enterocolitis in newborns. Like all medicines, Augmentin® is not recommended for use during pregnancy, unless the expected benefit to the mother exceeds the potential risk to the fetus.

    Breastfeeding period

    The drug Augmentin ® can be used during breastfeeding. With the exception of the possibility of developing sensitization, diarrhea, or candidiasis of the oral mucosa,associated with the penetration of the breast milk trace amounts of the active substances of this drug, no other adverse effects in children who are breastfed, was observed. In case of adverse effects in children who are breastfeeding, it is necessary to stop breastfeeding.

    Dosing and Administration:

    For oral administration.

    The dosage regimen is set individually depending on the age, body weight, function of the patient's kidneys, and also on the severity of the infection.

    To reduce potential abnormalities from the gastrointestinal tract and to optimize absorption, the drug should be taken at the beginning of the meal.

    Treatment should not last more than 14 days without reviewing the clinical situation.

    If necessary, stepwise therapy is possible (first intravenous injection of the drug Augmentin in the form of a powder for the preparation of a solution for intravenous administration, followed by the transition to the drug Augmentin in oral dosage forms).

    Adults and children 12 years of age or older or with a body weight of 40 kg or more

    For 1 tablet 875 mg / 125 mg 2 times a day.

    Special patient groups

    Children under 12 years of age with a body weight of less than 40 kg

    It is recommended to use other dosage forms of the drug Augmentin.

    Elderly patients

    No dosage adjustment is required. In elderly patients with impaired renal function, the dose should be adjusted as described below for adults with impaired renal function.

    Patients with impaired renal function

    Tablets 875 mg / 125 mg should be used only in patients with creatinine clearance greater than 30 ml / min, with no dosage adjustment required.

    In most cases, parenteral therapy should be preferred where possible.

    Patients with impaired hepatic function

    Treat with caution; regularly monitor liver function. There is insufficient data to change the recommendation of the dosing regimen in such patients.

    Side effects:

    The undesirable reactions presented below are listed in accordance with the damage to organs and organ systems and frequency of occurrence. Frequency of occurrence is defined as follows: very often (1/10), often (≥ 1/100 and <1/10), infrequently (≥ 1/1 000 and <1/100), rarely (≥ 1/10 000 and <1/1 000), very rarely (<1/10 000, including individual cases). Frequency categories were formed on the basis of clinical studies of the drug and post-registration surveillance.

    Frequency of occurrence of undesirable reactions

    Infectious and parasitic diseases

    Often: candidiasis of skin and mucous membranes.

    Violations of the blood and lymphatic system

    Rarely: reversible leukopenia (including neutropenia), reversible thrombocytopenia. Very rarely: reversible agranulocytosis and reversible hemolytic anemia, prolongation of bleeding time and prothrombin time, anemia, eosinophilia, thrombocytosis.

    Immune system disorders

    Very rarely: angioedema, anaphylactic reactions, a syndrome similar to serum sickness, allergic vasculitis.

    Disturbances from the nervous system

    Infrequent: dizziness, headache. Very rarely: reversible hyperactivity, convulsions. Seizures can occur in patients with impaired renal function, as well as in those who receive high doses of the drug. Insomnia, agitation, anxiety, behavior change.

    Disorders from the gastrointestinal tract

    Adults Very often: diarrhea. Often: nausea, vomiting.

    Children Often: diarrhea, nausea, vomiting.

    The entire population

    Nausea was most often associated with the use of high doses of the drug. If after the beginning of taking the drug there are undesirable reactions from the digestive tract, they can be eliminated if you take Augmentin at the beginning of the meal.

    Infrequent digestion. Very rarely: antibiotic-associated colitis (including pseudomembranous colitis and hemorrhagic colitis) (see section "Special instructions"), black "hairy" tongue, gastritis, stomatitis. Change in the color of the surface layer of tooth enamel in children.

    Disturbances from the liver and bile ducts

    Infrequent: moderate increase in activity of aspartate aminotransferase and / or alanine aminotransferase (ACT and / or ALT). This reaction is observed in patients receiving beta-lactam antibiotic therapy, but its clinical significance is unknown. Highly rarely: hepatitis and cholestatic jaundice. These reactions are observed in patients receiving penicillin antibiotics and cephalosporins. Increased concentrations of bilirubin and alkaline phosphatase.

    Undesirable reactions from the liver have been observed mainly in men and elderly patients and can be associated with long-term therapy.These undesirable reactions are very rare in children.

    These signs and symptoms usually occur in the process or immediately after the end of therapy, but in some cases may not appear for several weeks after the completion of therapy. Undesirable reactions are usually reversible.

    Undesirable reactions from the liver can be severe, in extremely rare cases there have been reports of lethal outcomes. In almost all cases, these were patients with severe concomitant pathologies or patients who received potentially hepatotoxic drugs at the same time.

    Disturbances from the skin and subcutaneous tissues

    Infrequent: rash, itching, hives. Rarely: erythema multiforme. Very rarely: Stevens-Johnson syndrome, toxic epidermal necrolysis, bullous exfoliative dermatitis, acute generalized exanthematous pustulosis.

    Disorders from the kidneys and urinary tract

    Very rarely: interstitial nephritis, crystalluria (see the section "Overdose"), hematuria.

    Overdose:

    There may be gastrointestinal disorders and disturbances in the water electrolyte balance.These overdose symptoms should be treated symptomatically, focusing on the normalization of the water-electrolyte balance. Amoxicillin crystalluria is described, in some cases leading to the development of renal failure.

    The drug "Augmentin ®" is excreted from the blood by hemodialysis.

    Interaction:

    Simultaneous use of the drug Augmentin® and probenecid is not recommended. Probenecid reduces the tubular secretion of amoxicillin, and therefore simultaneous use of the drug Augmentin and probenecid can lead to an increase and persistence in the blood concentration of amoxicillin, but not clavulanic acid.

    The simultaneous use of allopurinol and amoxicillin may increase the risk of skin allergic reactions. Currently, there is no data in the literature on the simultaneous use of a combination of amoxicillin with clavulanic acid and allopurinol. Penicillins can slow the excretion of methotrexate from the body by inhibiting its tubular secretion, so the simultaneous use of the drug Augmentin and methotrexate may increase the toxicity of methotrexate.

    Like other antibacterial drugs, the drug Augmentin can affect the intestinal microflora, leading to a decrease in absorption of estrogens from the digestive tract and a decrease in the effectiveness of combined oral contraceptives.

    In the literature, rare cases of an increase in the international normalized ratio (INR) in patients with joint use of acenocoumarol or warfarin and amoxicillin are described. If it is necessary to simultaneously prescribe the Augmentin® drug with anticoagulants, prothrombin time or INR should be carefully monitored with the appointment or discontinuation of the Augmentin® drug.) Correction of the dose of anticoagulants for oral administration may be required.

    In patients who received mycophenolate mofetil, after the start of the combination of amoxicillin with clavulanic acid, a decrease in the concentration of the active metabolite, mycophenolic acid, was observed, before taking the next dose of the drug by approximately 50%. Changes in this concentration can not accurately reflect the overall changes in the exposure of mycophenolic acid.

    Special instructions:

    Before starting treatment with Augmentin, you need to collect a detailed medical history,concerning previous hypersensitivity reactions to penicillins, cephalosporins or other substances that cause an allergic reaction in the patient. Serious, and sometimes lethal, hypersensitivity reactions (anaphylactic reactions) to penicillins are described. The risk of occurrence of such reactions is highest in patients who have a history of hypersensitivity reactions to penicillins. In case of an allergic reaction, it is necessary to stop treatment with the drug Augmentin® and begin the appropriate alternative therapy. Serious anaphylactic reactions should be promptly administered to the patient epinephrine. Oxygen therapy, intravenous glucocorticosteroids, and airway patency, including intubation, may also be required.

    In case of suspected infectious mononucleosis, the drug Augmentin® should not be used, since in patients with this disease amoxicillin can cause a skinlike skin rash, which makes it difficult to diagnose the disease. Long-term treatment with the drug Augmentin® can lead to excessive reproduction of insensitive microorganisms.

    In general, the drug Augmentin® is well tolerated and has a characteristic of all penicillins of low toxicity. During prolonged therapy with the drug Augmentin, it is recommended to periodically evaluate the function of the kidneys, liver and hematopoiesis.

    There are cases of pseudomembranous colitis occurring when taking antibiotics, the severity of which can range from mild to life-threatening. Therefore, it is important to consider the possibility of developing pseudomembranous colitis in patients with diarrhea during or after antibiotic use. If diarrhea is long or severe, or the patient experiences abdominal cramps, treatment should be stopped immediately and the patient should be examined.

    In patients who received a combination of amoxicillin with clavulanic acid in conjunction with indirect (oral) anticoagulants, in rare cases, increased prothrombin time (increased INR) was reported. With the joint appointment of indirect (oral) anticoagulants with a combination of amoxicillin and clavulanic acid, monitoring of the relevant indicators is necessary.To maintain the necessary effect of oral anticoagulants, correction of the dose of anticoagulants for oral administration may be required.

    In patients with reduced diuresis, crystalluria is very rare, mainly with parenteral therapy. During the administration of high doses of amoxicillin, it is recommended to take a sufficient amount of fluid and maintain an adequate diuresis to reduce the likelihood of amoxicillin crystals (see section "Overdose").

    When taking Augmentin®, a high content of amoxicillin in the urine is observed, which can lead to false-positive results in the determination of glucose in the urine (for example, the Benedict test, Feeling's test). In this case, it is recommended to use a glucose oxidant method for determining the concentration of glucose in the urine.

    Clavulanic acid can cause a non-specific binding of class G and albumin immunoglobulin to erythrocyte membranes, which leads to false positive results of Coombs test.

    Oral care helps prevent tooth discoloration associated with taking the drug, as it is enough to brush your teeth.

    Abuse and drug dependence

    There was no drug dependence, addiction and reactions of euphoria associated with the use of the drug Augmentin.

    Effect on the ability to drive transp. cf. and fur:The drug Augmentin® does not adversely affect these functions.
    Form release / dosage:

    Tablets coated with a film coating of 875 mg / 125 mg.

    Packaging:For 7 tablets in an Al / PVC blister. Each blister with a bag of silica gel is placed in a package of laminated aluminum foil. 2 packs of foil together with instructions for use are placed in a cardboard box.
    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 stated on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:П N015030 / 02
    Date of registration:24.09.2008 / 30.03.2010
    Expiration Date:Unlimited
    The owner of the registration certificate:GlaxoSmithKline Trading, ZAO GlaxoSmithKline Trading, ZAO Russia
    Manufacturer: & nbsp
    Representation: & nbspGlaxoSmithKline group of companies GlaxoSmithKline group of companies Unknown
    Information update date: & nbsp04.10.2017
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