The instruction for medical use
the Trade name
of Amoksiklav 2X
the International unlicensed name
Is not present
the Dosage form
Powder for preparation of suspension for intake, 457 mg / 5 ml, 8.75 g and 17.5 g
contain Structure of 5 ml of suspension (1 dosing pipette):
active agents: amoxicillin (in the form of trihydrate amoxicillin) 400.00 mg and clavulanic acid (in the form of clavulanate potassium) 57.00 mg.
excipients: the anhydrous citric acid crushed, sodium the citrate anhydrous crushed, cellulose microcrystalline and sodium the carboxymethylcellulose which is dried up, gum xanthane, silicon colloidal anhydrous, silicon dioxide, fragrance wild cherry, fragrance lemon, sodium the saccharin which is dried up, Mannitolum.
Crystal powder from white till yellow-white color. The prepared suspension uniform suspension from almost white till yellow color.
Antibacterial drugs for system use. Beta laktamnye antibacterial drugs Penicillin. Penicillin in a combination with inhibitors beta laktamaz. Clavulanic acid + amoxicillin.
The ATX J01CR02 code
Pharmacokinetics Amoxicillin properties and clavulanic acid, are completely dissolved in aqueous solution at physiological values rn organism environments. Both components are well absorbed after intake. To optimum accept amoxicillin/clavulanic acid in time or at the beginning of meal. After intake the bioavailability of amoxicillin and clavulanic acid is about 70%. Dynamics of concentration of drug in plasma of both components is similar. The maximum serumal concentration are reached 1 hour later after reception.
Concentration of amoxicillin and clavulanic acid in blood serum at reception of a combination of drugs of amoxicillin/clavulanic acid are similar to those which are observed at oral separate administration of an equivalent dose of amoxicillin and clavulanic acid.
About 25% of total amount of clavulanic acid and 18% of amoxicillin contact proteins in blood plasma. Distribution volume at oral administration of drug is about 0.3-0.4 l/kg of amoxicillin and 0.2 l/kg of clavulanic acid.
After intravenous administration, both amoxicillin, and clavulanic acid were found in a gall bladder, cellulose of an abdominal cavity, skin, fat, muscle tissue, synovial and peritoneal liquids, bile and pus. Amoxicillin badly gets into cerebrospinal fluid.
Amoxicillin and clavulanic acid get through a placental barrier. Both components pass also into breast milk.
Amoxicillin is partially removed with urine in the form of inactive penitsilloyny acid in the quantities equivalent to 10 – 25% of an initial dose. Clavulanic acid is metabolized in an organism and removed with urine and excrements and also in the form of carbon dioxide with expired air.
Average elimination half-life of amoxicillin/clavulanic acid makes about 1 hour, and average general clearance about 25 l/h. About 60 – 70% of amoxicillin and 40 – 65% of clavulanic acid are removed from an organism in an invariable view with urine during the first 6 h after reception of a single dose of tablets of amoxicillin/clavulanic acid. During various researches it was revealed that with urine 50-85% of amoxicillin and 27-60% of clavulanic acid within 24 hours are removed. The greatest number of clavulanic acid is removed within the first 2 hours after use.
Simultaneous use of a probenetsid slows down amoxicillin discharge, but this drug does not influence removal of clavulanic acid through kidneys.
Elimination half-life of amoxicillin is similar at children aged from 3 months up to 2 years, also at children of advanced age and adults. At prescription of medicine to very small children (including the premature newborn) in the first weeks of life, it is not necessary to administer the drug more often than two times a day that is connected with immaturity of a renal way of removal at children. Because elderly patients have renal dysfunction more often, it is necessary to appoint with care drug to this group of patients, but if it is necessary, it is necessary to carry out monitoring of renal function.
The general clearance of amoxicillin/clavulanic acid in plasma decreases in direct ratio to decrease in functions of kidneys. Decrease in clearance of amoxicillin is more significant in comparison with clavulanic acid as the bigger amount of amoxicillin is removed through kidneys. Therefore, when prescribing drug, dose adjustment is necessary for patients with a renal failure to prevent excessive accumulation of amoxicillin and to keep the necessary level of clavulanic acid.
When prescribing drug the patients should be careful with a liver failure when choosing a dose and to regularly control function of a liver.
Amoxicillin is a semi-synthetic antibiotic from group of penicillin (beta laktamny an antibiotic) which inhibits one or more enzymes (which are often mentioned as the proteins connecting penicillin), participating in biosynthesis of a peptidoglikan which is an important structural component of a wall of a bacterial cell. The inhibition of synthesis of a peptidoglikan leads to weakening of a wall of a cell which lysis of a cell and its death usually follows.
Amoxicillin collapses the beta lactamelements developed by resistant bacteria, and, therefore, the range of activity of one amoxicillin does not include the microorganisms producing these enzymes.
Clavulanic acid is the beta lactam which is structurally connected with penicillin. It inhibits some beta lactamelements, thereby preventing an amoxicillin inactivation, and expands its range of activity. Clavulanic acid in itself has no clinically significant antibacterial effect.
Time of exceeding is higher than the minimum overwhelming concentration (T & gt, MPK) it is considered the main determinant of efficiency of amoxicillin.
Two main mechanisms of resistance to amoxicillin and clavulanic acid are:
an inactivation bacterial beta lactamelements which are not suppressed with clavulanic acid, including classes B, C and D.
change penicillin of the connecting proteins that reduces affinity of antibacterial agent to the activator target.
The impermeability of bacteria or mechanisms of the effluxny pump (transport systems) can cause or maintain stability of bacteria, especially gram-negative bacteria.
The MPK boundary values for amoxicillin / clavulanic acid are those which are defined by the European Committee on testing of antimicrobial sensitivity (EUCAST).
Limits of sensitivity (mkg/ml)
Haemophilus influenzae1 & le, 1
& gt, 1
Moraxella catarrhalis1 & le, 1
& gt, 1
Staphylococcus aureus2 & le, 2
& gt, 2
& le, 0.25
& gt, 0.25
Enterococcus1 & le, 4
& gt, 8
Streptococcus A, B, C,
G5 & le, 0.25
& gt, 0.25
Streptococcus pneumoniae3 & le,
& gt, 2
& gt, 8
& le, 4
& gt, 8
& le, 4
& gt, 8
Boundary value without specific svyazi1
& gt, 8
1 Published values for concentration of amoxicillin. For determination
of sensitivity, concentration of clavulanic acid is fixed on 2 mg/l.
2 The published values of concentration of Oxacillinum.
3 Values of control points in the table are based on control points
4 Control point of resistance R & gt, 8 mg/l provide that all strains with
mechanisms of resistance are reported as resistant.
5 Values of control points in the table are based on control points
The prevalence of resistance can geographically vary also on time for the chosen types, and local information on resistance is desirable, especially at treatment of heavy infections.
Aerobic gram-positive microorganisms: Enterococcus faecalis, Gardnerella vaginalis, Staphylococcus aureus (sensitive to Methicillinum), Streptococcus agalacticae, Streptococcus pneumoniae, Streptococcus pyogenes and other beta and hemolytic streptococci, Streptococcus viridans group
Aerobic gram-negative microorganisms: Capnocyptophaga spp., Eikenella corrodens, Haemophilus influenzae, Moraxella catarrhalis, Pasteurella multocida
Anaerobic microorganisms: Bacteroides fragilis, Fusobacterium nucleatum, Prevotella spp.
Strains which acquired resistance, can cause difficulties
Aerobic gram-positive microorganisms: Enterococcus faecium
Aerobic gram-negative microorganisms: Escherichia coli, Klebsiella oxytoca, Klebsiella pneumoniae, Proteus mirabilis, Proteus vulgaris
Aerobic gram-negative microorganisms: Acinetobacter sp., Citrobacter freundii, Enterobacter sp., Legionella pneumophila, Morganella morganii, Providencia spp., Pseudomonas sp., Serratia sp., Stenotrophomonas maltophilia
of Chlamydophila pneumoniae, Chlamydophila psitacci, Coxiella burnetti, Mycoplasma pneumoniae
infections of a middle ear and sinusitis
of respiratory infection
of an infection of urinary tract, including prostatitis
of an infection of skin and soft tissues, including periodontal fabrics
of an infection of bones and joints
the Route of administration and doses
of the Dose are calculated taking into account the content of amoxicillin/clavulanic acid. When choosing a dose of the drug Amoxiclav 2X for treatment of separate infections it is necessary to consider:
sensitivity of the activator to an antibiotic
severity and localization of an infection
age, weight and function of kidneys of the patient, as shown below.
It is also necessary to consider other routes of administration of the drug Amoxiclav 2X, for example, to use higher doses of amoxicillin and/or to appoint amoxicillin and clavulanic acid in various ratios.
Suspension is accepted orally before meal to reduce possible gastrointestinal disturbances and to increase absorption of amoxicillin/clavulanic acid.
Adults and children weighing more than 40 kg
the Recommended dosage to adults and children weighing more than 40 kg makes 1750 mg / 250 the mg divided into two receptions.
Usually suspensions are not appointed to children weighing more than 40 kg.
To children with body weight less than 40 kg
the Daily dose at children less than 40 kg of body weight makes from 25 mg / 3.6 mg/kg up to 45 mg / 6.4mg/kg body weights, divided into two receptions.
In heavier infections (otitis of a middle ear, sinusitis and lower respiratory tract infections) the daily dose at children makes 70 mg / 10 mg/kg, divided into two receptions.
The doser (dosing pipette) for a suspension dosage is applied.
The table of the choice of a single dose of the drug Amoxiclav 2X, 457 mg / 5 ml depending on body weight
The body weight (kg)
the Daily dose of amoxicillin
mg/kg/days 45 mg/kg/days 70 mg/kg/days
5 0,8 ml 2 times in day
of 1.4 ml 2 times a day
6 0,9 ml 2 times in day
of 1.7 ml 2 times a day
7 1,1 ml 2 times in day
of 2.0 ml 2 times a day
8 1,3 ml 2 times in day
of 2.3 ml 2 times a day
9 1,4 ml 2 times in day
of 2.5 ml 2 times a day
10 1,6 ml 2 times in day
of 2.8 ml 2 times a day
11 1,7 ml 2 times in day
of 3.1 ml 2 times a day
12 1,9 ml 2 times in day
of 3.4 ml 2 times a day
13 2,0 ml 2 times in day
of 3.7 ml 2 times in day
of 5.7 ml 2 times a day
14 2,2 ml 2 times in day
of 3.9 ml 2 times in day
of 6.0 ml 2 times a day
15 2,3 ml 2 times in day
of 4.2 ml 2 times in day
of 6.5 ml 2 times a day
20 3,1 ml 2 times in day
of 5.6 ml 2 times in day
of 8.8 ml 2 times a day
25 4,0 ml 2 times in day
of 7.0 ml 2 times in day
of 11 ml 2 times a day
30 4,7 ml 2 times in day
of 8.5 ml 2 times in day
of 13 ml 2 times a day
35 5,5 ml 2 times in day
of 9.8 ml 2 times in day
of 15.3 ml 2 times a day
40 6,3 ml 2 times in day
of 11.3 ml 2 times in day
of 17.5 ml 2 times a day
Are absent clinical these uses of this dosage of the drug Amoxiclav 2X over 45 mg / 6.4 mg/kg/days at children 2 years are younger.
Due to the lack of data on use
of the drug Amoxiclav of 2X 457 Mg / 5 of ml for children 2 months are younger, do not appoint drug to children up to 2 months.
For children with body weight less than 40 kg the maximum daily dose makes 2400 mg of amoxicillin / 600 clavulanic acid mg. In need of purpose of higher daily dose of amoxicillin, it is necessary to appoint other dosage of the drug Amoxiclav 2X in order to avoid reception of high doses of clavulanic acid needlessly.
Duration of treatment depends on reaction of the patient. Some infections (for example, osteomyelitis) demand longer period of treatment. The maximum time of therapy should not exceed 14 days.
The renal failure
Dose adjustment is not required when prescribing drug to patients with clearance of creatinine (CrCl) more than 30 ml/min.
The drug Amoxiclav 2X (ratio of amoxicillin and clavulanic acid 7:1) is not recommended to appoint to patients with clearance of creatinine less than 30 ml/min. (0.5 ml/sec.) as there are no recommendations about dose adjustment.
The liver failure
to Apply with care. It is necessary to check function of a liver regularly.
A way of preparation of suspension
the Drug Amoxiclav 2X, suspension of 457 mg / 5 ml (8.75 g of powder in bottles with a capacity of 60 ml for preparation of 35 ml of suspension): to stir up a bottle with powder, to add 29.5 ml of water in two steps (at first on 2/3 and then to a tag). It is good to shake up bottle contents before each reception. The volume of the prepared suspension of 35 ml.
The drug Amoxiclav 2X, suspension of 457 mg / 5 ml (17.5 g of powder in bottles with a capacity of 100 ml for preparation of 70 ml of suspension): to stir up a bottle with powder, to add 59 ml of water in two steps (at first on 2/3 and then to a tag). It is good to shake up bottle contents before each reception. The volume of the prepared suspension of 70 ml.
Classification of side effects by emergence frequency:
very often 1/10, is frequent from 1/100 to 1/10, infrequently from 1/1000 to 1/100, 1/10000 is rare from 1/10000 to 1/1000, very seldom, frequency is unknown (the available data are not enough for performance of assessment).
candidiasis (skin and mucous membranes)
dizziness, a headache
a digestive disturbance
increase in level of nuclear heating plant and/or ALT5
skin syp7, zud7, krapivnitsa7
the passing leukopenia (including a neutropenia), thrombocytopenia
Frequency is unknown:
growth of insensitive organisms
a passing agranulocytosis, hemolytic anemia, increase in a bleeding time and prothrombin vremeni1
angioneurotic otek10, anafilaksiya10, syvorotochno-like sindrom10, allergic vaskulit10
passing hyperactivity, sudorogi2
an antibiotic – the associated kolit4, black fleecy language, coloring change zubov11
gepatit6, cholestatic zheltukha6
Stephens-Johnsona7 syndrome, toxic epidermal nekroliz7, violent exfoliative dermatit7, sharp generalized exanthematous pustulez (AGEP)9
kristalluriya8 1 cm undressed Special instructions.
2 cm undressed Special instructions.
3 Nausea are more often at use of higher doses inside. It is possible to reduce
gastrointestinal reactions, accepting amoxicillin / clavulanic acid
at the beginning of meal.
4 Including pseudomembranous colitis and hemorrhagic colitis (see the section Special
5 moderate increase in level of nuclear heating plant and/or ALT at the patients
accepting beta laktamnye antibiotics Was noted, but the value of these results is unknown.
6 These complications were noted when using drug in combination with other
penicillin and cephalosporins (see the section Special instructions).
7 At emergence of any skin reaction of hypersensitivity, treatment should
be stopped (see the section Special instructions).
8 cm undressed Special instructions.
9 cm section of the Contraindication.
10 cm undressed Special instructions.
11 very exceptional cases of change of coloring of a surface of teeth at
children Were registered. Observance of rules of hygiene of a mouth will help to prevent it.
Toothbrushing removes drug from an oral cavity.
hypersensitivity to active agent or any auxiliary component of drug
heavy reaction of hypersensitivity in the anamnesis to others beta laktamnym to drugs (for example, to cephalosporins, karbapenema or monobaktama)
cholestatic jaundice or other cases of a liver failure in the anamnesis (in connection with use of amoxicillin / clavulanic acid)
Oral anticoagulants and antibiotics of penicillinic group are widely used in practice without messages about interaction. However in references the increase in the international normalized relation at the patients accepting atsenokumarol or warfarin together with amoxicillin was noted. If simultaneous use of drugs is necessary, it is necessary to control carefully a prothrombin time or the international normalized relation during the assigning and cancellation of amoxicillin. Moreover, change in a dosage of oral anticoagulants can be required.
Drugs of penicillinic group can reduce removal of a methotrexate that causes potential increase in toxicity.
Nie is recommended simultaneous use of a probenetsid. Probienieqid reduces renal canalicular secretion of amoxicillin. Sharing with the drug Amoxiclav 2X can lead to increase in levels of amoxicillin in blood, but not clavulanic acid.
Simultaneous use of Allopyrinolum and drug Amoxiclav 2X can increase risk of emergence of allergic reactions. Data on simultaneous use of Allopyrinolum and the drug Amoxiclav 2X are absent now.
At the patients accepting mikofenolat mofetit, at combined use with the drug Amoxiclav 2X the concentration of an active metabolite of mikofenolovy acid when assigning an initial dose decreases approximately by 50%. Change of level of concentration of an initial dose can not correspond to change of total concentration of mikofenolovy acid.
before therapy by amoxicillin/clavulanic acid it is necessary to study carefully existence at the patient of reactions of hypersensitivity to penicillin, cephalosporins or others beta laktamnye substances.
Serious and sometimes deadly (anaphylactic) reactions of hypersensitivity were registered at the patients receiving treatment by penicillin. These reactions meet at people with reaction of hypersensitivity to penicillin and an atopy in the anamnesis more often. At development of allergic reaction to amoxicillin/clavulanic acid it is necessary to stop therapy by this drug and to pass to other alternative treatment.
In case the infection was resistant to amoxicillin, it is necessary to consider the possibility of use of amoxicillin/clavulanic acid instead of amoxicillin.
At high risk of resistance of the activator to a beta laktamnym the antibiotics should not use the drug Amoxiclav 2X. It is not recommended to use drug for treatment resistant to S. pneumoniae penicillin.
At patients with a renal failure and accepting a high dose of drug, spasms can develop.
It is not necessary to appoint amoxicillin/clavulanic acid in an infectious mononucleosis as appearance of korepodobny rash is possible (to amoxicillin).
Simultaneous use of Allopyrinolum during treatment by amoxicillin can increase a likelihood of development of skin allergic reactions. Data on simultaneous use of Allopyrinolum and the drug Amoxiclav 2X are absent now.
Prolonged use of drug can cause the overgrowth of insensitive microorganisms.
Emergence in an initiation of treatment of a generalized erythema with pustulous rashes and fever can be a symptom of development of a sharp generalized exanthematous pustulez. At development of this reaction it is required to stop use of the drug Amoxiclav 2X and not to use amoxicillin in the future any more.
Patients should appoint drug with care with a liver failure.
Cases of appearance of abnormal liver functions were registered generally at men and elderly patients, quite seldom met at children who took the drug during the long span. Signs and symptoms usually develop in time or right after an initiation of treatment, but in certain cases can be shown only in several weeks after the therapy termination. These symptoms are usually reversible. Complications from a liver can be expressed in a severe form and in extremely exceptional cases to proceed from the death. They almost always develop at patients with serious associated diseases or at the patients taking other drugs which influence a liver.
Development an antibiotic – the associated colitis is characteristic of any antibacterial drugs, including amoxicillin, and can vary on degree of manifestation from moderated to zhizneugrozhayushchy. Therefore, it is important to consider this diagnosis when prescribing drug to patients, having diarrhea, in time or after use of any antibiotics. At emergence an antibiotic – the associated colitis, it is necessary to stop use of the drug Amoxiclav 2X immediately. After consultation of the doctor the corresponding therapy has to be appointed. The drugs reducing a vermicular movement are contraindicated in this situation.
At long therapy it is regularly recommended to estimate function of systems of bodies, including kidneys, a liver and the haematogenic function.
It is necessary correction of a dose of oral anticoagulants for maintenance of desirable level of fibrillation.
At patients with disturbances of functions of kidneys, correction of a dose depending on the degree of manifestation of disturbances is required.
At patients with a reduced diuresis, the crystalluria was very seldom noted, mainly during parenteral therapy. During treatment recommend to the patient plentifully drink to avoid possible development of a crystalluria. According to the obtained data amoxicillin accumulates in bladder catheters (mainly at intravenous administration of high doses), in this case it is necessary to control passability of a catheter regularly.
During treatment using amoxicillin it is necessary to use enzymatic methods of glucose oxydas when carrying out analyses on presence of glucose in urine as when using not of enzymatic methods false positive results are possible.
Presence of clavulanic acid in the drug Amoxiclav 2X can lead to nonspecific binding of immunoglobulin G and albumine with membranes of erythrocytes and to false positive results of test of Koombs.
Data on positive takes of the analysis of Bio-Rad Laboratories Platelia Aspergillus EIA at the patients accepting amoxicillin/clavulanic acid which were Aspergillus which are not infected with an infection subsequently were obtained, but there are no data on cross-reactions using non-Aspergillus of polysaccharides and polifuranoz. Thus, positive takes of analyses of the patients accepting amoxicillin/clavulanic acid should be interpreted with care and to confirm with other diagnostic methods.
of the Research animals is not indicated direct or indirect harmful effects concerning pregnancy, by development of an embryo / fruit, childbirth or post-natal development.
Now there is a limited amount of data on use of amoxicillin/clavulanic acid during pregnancy at the person which did not reveal the increased risk of congenital malformations. In clinical trial at women with a premature rupture of a fetal membrane the relationship of cause and effect between preventive treatment using amoxicillin / clavulanic acid and the increased risk of a necrotic coloenteritis at the newborn was registered. It is not recommended to use the drug Amoxiclav 2X during pregnancy, use is possible only in urgent cases on doctor’s orders.
Both active agents are emitted in breast milk (there are no data on influence of clavulanic acid on breastfeeding). Therefore, when breastfeeding the emergence of such symptoms as a diarrhea and fungal infections of mucous membranes is possible, in these cases it is necessary to stop breastfeeding. The drug Amoxiclav 2X is allowed to be used during feeding by a breast only after advantage/risk assessment by the attending physician.
Features of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms
of Researches on identification of the effects influencing an opportunity to drive the car and the equipment it was not carried out. Nevertheless, the drug Amoxiclav 2X can cause such side effects as allergic reactions, dizziness, spasms which can affect an opportunity to drive the car and moving mechanisms.
Symptoms: gastrointestinal symptoms and disturbances of water and electrolytic balance are possible. The amoxicillin crystalluria in certain cases leads to a renal failure. At patients with renal failures or at the patients accepting high doses of drug spasms are possible.
Treatment: symptomatic treatment taking into account water and electrolytic balance. Amoxicillin/clavulanic acid can be brought out of an organism by means of a hemodialysis.
A form of release and packing
On 8.75 g of powder in bottles (capacity of 60 ml) or on 17.5 g of powder in the bottles (capacity of 100 ml) from glass of amber color corked by the screwing-up polyethylene covers with a strip of control of the first opening. On 1 bottle together with the dosing pipette and the instruction for medical use in the state and Russian languages place in a pack from cardboard.
To Store storage conditions in the dry place at a temperature not over 25 of C.
To store out of children’s reach!
Period of storage
To store the prepared suspension in the fridge (at a temperature from 2 With to 8 C) no more than 7 days, in densely closed bottle.
Not to use after the expiry date specified on packing.
According to the prescription
the Producer / Packer Lek Pharmasyyutikals of of, Slovenia
of Perzonali 47, SI 2391 Prevalje, Slovenia
the Owner of the registration certificate
Lek Pharmasyyutikals of of, Slovenia
of Verovskova, 57, 1526 Ljubljana, Slovenia
the Address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of the products (goods) responsible for post-registration observation of safety of medicine
Representative office of JSC Sandoz Pharmasyyutikals of of in Republic of Kazakhstan, Almaty, Luganskogo St. 96