Composition
One bottle of powder for preparing a solution for intravenous and intramuscular use contains:
Active ingredient: Â ceftriaxone sodium – 2.142 g (in terms of ceftriaxone-2 g).
Pharmacological action
Pharmacotherapy group
Antibiotic-cephalosporin
ATX code
J01DD04
Pharmacodynamics :
Ceftriaxone is a parenteral cephalosporin antibiotic of the third generation.
The bactericidal activity of ceftriaxone is due to the suppression of cell wall synthesis.
In vitro, ceftriaxone has a broad spectrum of action against gram-negative and gram-positive microgranisms. It is highly resistant to most beta-lactamases (both penicillinases and cephalosporinases) produced by gram-positive and gram-negative bacteria.
Ceftriaxone is usually active against the following microorganisms.
Gram
-positive aerobes Staphylococcus aureus (msticillin-sensitive) coagulase-negative staphylococci Streptococcus pyogenes (β-hemolytic group A) Streptococcus agalactiae (β-hemolytic group B) β-hemolytic streptococci (groups neither A nor B) Streptococcus viridans Streptococcus pneumoniae.
Note. Methicillin-resistant Staphylococcusspp. are resistant to cephalosporins, including ceftriaxone. Generally Enterococcusfaecalis Enterococcusfaecium and Listeriamonocytogenes are also resistant.
Gram-negative aerobes
Acinetobacter Iwoffii Acinetobacteranitratus (mainly A. baumannii)* Aeromonashydrophila Alcaligenesfaecalis Alcaligenesodorans alkaligene-like bacteria Borreliaburgdorferi Capnocytophagaspp. Citrobacterdiversus (including C. amalonaticus) Citrobacterfreundii* Escherichiacoli Enterobacteraerogenes* Enterobactercloacae* Enterobacterspp. (other)* Haemophilusducreyi Haemophilusinfluenzae Haemophilusparainfluenzae Hafniaalvei Klebsiellaoxytoca Klebsiellapneumoniae** Moraxellacatarrhalis(formerly known as Branhamellacatarrhalis) Moraxellaosloensis Moraxellaspp. (others) Morganella morganii Neisseria gonorrhoeae. Neisseria meningitidis Pasteurella multocida Plesiomonas shigelloides Proteus mirabilis Proteus penneri* Proteus vulgaris* Pseudomonas fluorescens* Pseudomonas spp. (other) Providencia rettgeri* Providencia spp. (other) Salmonella typhi Salmonella spp. (non-typhoid) Serratia marcescens * Serratia spp. (other)* Shigella spp. Vibrio spp. Yersinia enterocolitica Yersinia spp. (other).
* Some isolates of these species are resistant to ceftriaxone mainly due to the formation of beta-lactamases encoded by chromosomes.
** Some isolates of these species are stable due to the formation of a number of plasmid-mediated β-lactamases.
Note. Many strains of the above mentioned microorganisms that are polyresistant to other antibiotics such as aminopenicillins and ureidonenicillins first and second generation cephalosporins and aminoglycosides are sensitive to ceftriaxone. Treponoma pallidum is sensitive to ceftriaxone in vitro and in animal experiments. Clinical trials show that ceftriaxone has good efficacy against primary and secondary syphilis. With very few exceptions, clinical isolates of P. aeruginosa are resistant to ceftriaxone.
Anaerobes
Bacteroidesspp. (bile-sensitive)*Â Clostridiumspp. (except with. difficile) Fusobacterium nucleatum Fusobacterium spp. (others)Â Gaffkya anaerobica (formerly called Peptococcus) Peptostreptococcus spp.
* Some isolates of these species are resistant to ceftriaxone due to the formation of β-lactamases. Note. Many strains of beta-lactamase-forming Bacteroidesspp. (in particular B. fragilis) they are stable. Clostridium Difficile is also stable.
Sensitivity to ceftriaxone can be determined by the disco-diffusion method or by serial dilutions on agar or broth using a standard method similar to that recommended by the Institute of Clinical and Laboratory Standards (ICLS). The ICLS has established the following criteria for evaluating the results of a sample for ceftriaxone: :
Sensitive |
Moderately sensitive |
Sustainable |
|
Dilution method |
= 8 |
16-32 |
= 64 |
Suppressive concentration mg / l |
|||
Disc method (disc containing 30 mcg of ceftriaxone) = 21 |
20-14 |
= 13 |
|
Diameter of the growth retardation zone mm |
Ceftriaxone discs should be used for determination since in vitro studies have shown that ceftriaxone is active against individual strains that show resistance when using discs designed for the entire group of cephalosporins.
Instead of ICLS standards, other well-standardized standards can be used to recommend determining the sensitivity of microorganisms, for example, the German Institute for Standardization DIN (Deutsches Institut fur Normung) and the international recommendations of ICS (International Collaborative Study), which allow an adequate interpretation of the sensitivity state.
Pharmacokinetics:
The pharmacokinetics of ceftriaxone are non-linear. All major pharmacokinetic parameters based on total drug concentrations, with the exception of the half-life, depend on the dose and increase less than in proportion to its increase. Non-linearity is typical for pharmacokinetic parameters that depend on the total concentration of ceftriaxone in blood plasma (not only free ceftriaxone) and is explained by saturation of the drug’s binding to plasma proteins.
Suction
The maximum plasma concentration after a single intramuscular injection of 1 g of the drug is about 81 mg / l and is reached within 2-3 hours after use. The areas under the plasma concentration – time curve after intravenous and intramuscular use are the same. This means that the bioavailability of ceftriaxone after intramuscular use is 100%.
After intravenous bolus use of 500 mg and 1 g of ceftriaxone, the mean maximum plasma concentrations were 120 mg / l and 200 mg/L, respectively. After an intravenous infusion of 500 mg of 1 g and 2 g of ceftriaxone, the plasma concentrations of the drug were approximately 80-150 and 250 mg/l, respectively. After intramuscular injection, the average maximum concentration of ceftriaxone in blood plasma is approximately two times lower than after intravenous use of the equivalent dose of the drug.
Distribution
The volume of distribution of ceftriaxone is 7-12 liters. After use in a dose of 1-2 g, ceftriaxone penetrates well into tissues and body fluids. For more than 24 hours, its concentrations far exceed the minimum suppressive concentrations for most infectious agents in more than 60 tissues and fluids (including the lungs, heart, bile ducts, liver, tonsils, middle ear and nasal mucosa, bones, as well as spinal pleural and synovial fluids and prostate secretions).
After intravenous use, ceftriaxone quickly penetrates into the cerebrospinal fluid, where bactericidal concentrations against sensitive microorganisms persist for 24 hours.
Protein binding
Ceftriaxone reversibly binds to albumin. The degree of binding is approximately 95% when the plasma concentration of ceftriaxone is at least 100 mg/l.
The concentration of ceftriaxone bound to plasma protein decreases as its concentration increases, since the binding is saturated and amounts to about 85% at concentrations of 300 mg/l.
Penetration into individual tissues
Ceftriaxone penetrates through the meninges to the greatest extent when they are inflamed. The average maximum concentration of ceftriaxone in the cerebrospinal fluid reaches 25% of the concentration of ceftriaxone in the blood plasma in patients with bacterial meningitis and only 2% of the concentration in the blood plasma in patients with non-inflamed meninges. The maximum concentration of ceftriaxone in the cerebrospinal fluid is reached 4-6 hours after its intravenous use. Ceftriaxone passes through the placental barrier and enters breast milk in low concentrations.
Metabolism
Ceftriaxone does not undergo systemic metabolism and is converted to inactive metabolites by the action of intestinal microflora.
Deduction
The total plasma clearance of ceftriaxone is 10-22 ml/min. Renal clearance is 5-12 ml / min. 50-60% of ceftriaxone is excreted unchanged by the kidneys and 40-50% – unchanged by the intestines. The half-life of ceftriaxone in adults is about 8 hours.
Pharmacokinetics in special clinical cases
Newborns infants and children under 12 years of age
In newborns, the half-life of ceftriaxone is increased compared to other age groups.In the first 14 days of life, the concentration of free ceftriaxone in blood plasma can be further increased due to low glomerular filtration and features of binding of the drug to plasma proteins. In paediatric patients, the half-life is shorter than in newborns and adults.
The values of plasma clearance and volume of distribution of total ceftriaxone are higher in newborns, children and children under 12 years of age compared to those in adults.
Impaired kidney or liver function
In patients with impaired renal or hepatic function, the pharmacokinetics of ceftriaxone change slightly, there is only a small increase in the half-life (less than 2 times), even in patients with severe renal insufficiency.
A slight increase in the half-life of ceftriaxone in renal insufficiency can be explained by a compensatory increase in non-renal clearance as a result of a decrease in the degree of binding to plasma proteins and a corresponding increase in the non-renal clearance of total ceftriaxone.
In patients with hepatic insufficiency, the elimination half-life does not increase. In such patients, a compensatory increase in renal clearance occurs. The reason is also an increase in the concentration of free ceftriaxone in blood plasma, which contributes to a paradoxical increase in the total clearance of the drug against the background of an increase in the volume of distribution.
Senile patients
In patients over 75 years of age, the elimination half-life is on average two or three times longer than in adult patients.
Indications
Infections caused by ceftriaxone-sensitive pathogens: sepsis; meningitis; disseminated Lyme disease (stages II and III of the disease); abdominal infections (peritonitis biliary tract and gastrointestinal tract infections); infections of bones, joints, soft skin tissues and wound infections; infections in patients with weakened immune systems; kidney and urinary tract infections; respiratory tract infections especially pneumonia and ENT infections; genital infections including gonorrhea.
Perioperative prevention of infections.
Use during pregnancy and lactation
Pregnancy
Ceftriaxone penetrates the placental barrier. The safety of use during pregnancy in women has not been established. Preclinical studies of reproduction have not revealed embryotoxic fetotoxic teratogenic effects or other adverse effects of the drug on male and female fertility the process of childbirth perinatal and postnatal fetal development. During pregnancy, especially in the first trimester, it should be prescribed only for strict indications, provided that the intended benefit to the mother exceeds the potential risk to the fetus.
Breast-feeding period
In low concentrations, ceftriaxone passes into breast milk. The effect of ceftriaxone on a breastfed child is unlikely when used by the mother in therapeutic doses, however, the risk of diarrhea, fungal infections of the mucous membranes and hypersensitivity reactions in the child cannot be excluded.
It is necessary to stop breastfeeding or stop / refrain from ceftriaxone therapy, taking into account the benefits of breastfeeding for the child and the benefits of therapy for the mother.
Contraindications
Hypersensitivity
Hypersensitivity to ceftriaxone and any other component of the drug.
Hypersensitivity to cephalosporins.
A history of severe hypersensitivity reactions (e. g. anaphylactic reactions) to other beta-lactam antibiotics (penicillins, monobactams, and carbapenems).
Premature babies
Ceftriaxone is contraindicated in premature children under 41 weeks of age (total gestational and chronological age).
Full-term newborns (
Hyperbilirubinemia jaundice or acidosis hypoalbuminemia in newborns (in vitro studies have shown that ceftriaxone can displace bilirubin from binding to serum albumin, increasing the risk of bilirubin encephalopathy in such patients).
Intravenous use of potassium-containing solutions to newborns.
Newborns (≤28 days) who are already prescribed or are expected to receive intravenous treatment with calcium-containing solutions, including prolonged calcium-containing infusions, for example, with parenteral nutrition due to the risk of precipitation of ceftriaxone calcium salts (see sections “Dosage and use” and “Interaction with other drugs”).
Isolated fatal cases of precipitation in the lungs and kidneys in newborns treated with ceftriaxone and calcium-containing solutions are described. At the same time, in some cases, one venous approach was used and precipitation formation was observed directly in the system for intravenous use. At least one fatal case was also described with different venous approaches and at different times of use of ceftriaxone and calcium-containing solutions. Such cases were observed only in newborns (see the section “Post-marketing surveillance”).
Lidocaine
Before performing an intramuscular injection of ceftriaxone using lidocaine, it is necessary to exclude the presence of contraindications to lidocaine. Contraindications to the use of lidocaine are given in the instructions for medical use of lidocaine. Ceftriaxone solutions containing lidocaine should not be administered intravenously.
With caution:
Breast-feeding period.
A history of mild hypersensitivity reactions to other beta-lactam antibiotics (penicillins, monobactams, and carbapenems).
Side effects
The most common adverse reactions reported during ceftriaxone therapy in clinical studies are eosinophilia leukopenia thrombocytopenia diarrhea rash and increased activity of liver enzymes.
The following classification is used to describe the frequency of adverse reactions: very frequent (≥1/10) frequent (≥1/100 and <1/10) infrequent (≥1/1000 and <1/100) rare (≥1/10000 and <1/1000) and very rare (
Adverse reactions are grouped according to the classes of organ systems in the MedDRA Regulatory Dictionary.
Infectious and parasitic diseases:Â infrequently-mycoses of the genital organs; rarely-pseudomembranous colitis.
Disorders of the blood and lymphatic system:Â often – eosinophilia, leukopenia, thrombocytopenia; infrequently-granulocytopenia, anemia, coagulopathy.
Nervous system disorders:Â infrequently – headache and dizziness.
Respiratory, thoracic and mediastinal disorders:Â rarely-bronchospasm.
Disorders of the gastrointestinal tract:Â often – diarrhea unformed stools; infrequently nausea and vomiting.
Liver and biliary tract disorders:Â often-increased activity of liver enzymes (aspartate aminotransferase (ATS) alanine aminotransferase (ALT) alkaline phosphatase (ALP)).
Skin and subcutaneous tissue disorders:Â often-rash; infrequently-pruritus; rarely-urticaria.
Kidney and urinary tract disorders:Â rarely-hematuria glucosuria.
General disorders and disorders at the injection site:Â infrequently-phlebitis pain at the injection site fever; rarely-edema chills.
Influence on the results of laboratory and instrumental studies:Â infrequently-an increase in the concentration of creatinine in the blood.
Post-registration monitoring
Side effects observed with the use of Ceftriaxone-AKOS in the post-marketing period are described below. Determining the frequency of observed adverse events and their association with the use of Ceftriaxone-ACOS is not always possible, as it is impossible to determine the exact size of the patient population.
Disorders of the gastrointestinal tract:Â pancreatitis stomatitis glossitis taste disorder.
Blood disorders of the lymphatic system: thrombocytosis increased thromboplastin and prothrombin time decreased prothrombin time hemolytic anemia. Individual cases of agranulocytosis are described (
Immune system disorders:Â anaphylactic shock hypersensitivity Yarisch-Herxheimer reaction.
Skin and subcutaneous tissue disorders:Â acute generalized exanthematous pustulosis isolated cases of severe adverse reactions (exudative erythema multiforme Stevens-Johnson syndrome toxic epidermal necrolysis (Lyell’s syndrome) drug reaction with eosinophilia and systemic symptoms (DRESS syndrome).
Nervous system disorders:Â convulsions.
Hearing disorders and labyrinth disorders:Â vertigo.
Infectious and parasitic diseases:Â superinfections.
The following adverse reactions are also known:Â formation of precipitates of cefritaxone calcium salts in the gallbladder with appropriate symptoms bilirubin encephalopathy hyperbilirubinemia oliguria vaginitis increased sweating “hot flashes” allergic pneumonitis nosebleeds jaundice palpitation sensation serum sickness as well as anaphylactic or anaphylactoid reactions.
Separate fatal cases of precipitate formation in the lungs and kidneys are described based on autopsy results in newborns treated with cefritaxone and potassium-containing solutions. In some cases, a single venous approach was used and the formation of precipitates was observed directly in the system for intravenous use.At least one fatal case has also been reported with different venous approaches and at different times of use of ceftriaxone and calcium-containing solutions. At the same time, according to the results of an autopsy study, no precipitates were found in this newborn. Such cases were observed only in newborns (see the section “Special instructions”).
Cases of formation of ceftriaxone precipitates in the urinary tract have been reported mainly in children who received either large daily doses of the drug (≥80 mg / kg per day) or cumulative doses of more than 10 g and who also had additional risk factors (dehydration, bed rest). The formation of precipitates in the kidneys can be asymptomatic or clinically manifested, can lead to ureteral obstruction and postrenal acute renal failure. This adverse event is reversible and disappears after discontinuation of therapy with Ceftriaxone-AKOS.
General disorders and disorders at the injection site:Â phlebitis after intravenous use. It can be avoided by injecting the drug slowly for 5 minutes, preferably into a large vein.
Intramuscular injection without lidocaine is painful.
Influence on the results of laboratory tests
When treated with Ceftriaxone-ACOS, patients may have false positive Coombs test results. Like other antibiotics, Ceftriaxone-AKOS can give a false positive test result for galactosemia. False positive results can also be obtained when determining glucose in the urine by non-enzymatic methods, therefore, during therapy with Ceftriaxone-AKOS, glucosuria, if necessary, should be determined only by the enzyme method.
Ceftriaxone may cause an unreliable decrease in the glycemic values obtained with certain blood glucose monitoring devices. See the instructions in the instructions for use of the device used. If necessary, alternative methods for determining blood glucose should be used.
Interaction
Concomitant use of high doses of Ceftriaxone-ACOS and loop diuretics (for example, furosemide) did not cause renal impairment. There are conflicting data on the likelihood of increased nephrotoxicity of aminoglycosides when used with cephalosporins, so it is necessary to monitor renal function and the concentration of aminoglycosides in the blood. Alcohol consumption after use of Ceftriaxone-AKOS was not accompanied by a disulfiram-like reaction. Ceftriaxone does not contain the N-methylthiotetrazole group that could cause ethanol intolerance and bleeding, which is common with some other cephalosporins. Probenecid does not affect the elimination of Ceftriaxone-AKOS.
Bacteriostatic antibiotics reduce the bactericidal effect of ceftriaxone.
Antagonism between chloramphenicol and ceftriaxone was found in vitro.
Do not use calcium-containing solvents such as Ringer’s solution or Hartmann’s solution when preparing solutions of Ceftriaxone-AKOS for intravenous use and their subsequent dilution due to the possible formation of precipitates. The formation of ceftriaxone calcium salt precipitates can also occur when Ceftriaxone-AKOS is mixed with calcium-containing solutions using a single venous approach. Do not use ceftriaxone simultaneously with calcium-containing solutions for intravenous use, including long-term infusions of calcium-containing solutions, for example, parenteral nutrition using a Y-connector. For all groups of patients except newborns, sequential use of ceftriaxone and calcium-containing solutions is possible, with careful flushing of the infusion systems between infusions with a compatible liquid. To assess the interaction of Ceftriaxone and calcium with water, two in vitro studies were conducted, one using adult blood plasma and the other using umbilical cord blood plasma from a newborn. Various combinations of ceftriaxone with an initial concentration of up to 1 mM (the maximum concentration that ceftriaxone reaches in vivo with an infusion of 2 g of the drug for at least 30 minutes) and calcium with an initial concentration of up to 12 mM (48 mg/dl) were analyzed. A decrease in the concentration of ceftriaxone in plasma was observed when using calcium at a concentration of 6 mM (24 mg / dl) or higher for adult plasma and at a concentration of 4 mM (16 mg / dl) or higher for neonatal plasma, which indicates an increased risk of formation of ceftriaxone calcium salts in newborns (see sections “Dosage and use” and “Contraindications”).
Ceftriaxone is pharmacologically incompatible with amsacrine vancomycin fluconazole and aminoglycosides.
When using vitamin K antagonists on the background of therapy with Ceftriaxone-AKOS, the risk of bleeding increases. Blood clotting parameters should be constantly monitored and, if necessary, the anticoagulant dose adjusted both during and after the end of Ceftriaxone-ACOS therapy.
Synergy between ceftriaxone and aminoglycosides has been shown for many gram-negative bacteria. Although the increased effectiveness of such combinations is not always predictable it should be borne in mind for severe life threatening infections such as those caused by Pseudomonas Aeruginosa.
How to take, course of use and dosage
Standard dosage regimen
Intravenous intramuscular injection.
Adults and children over 12 years of age ≥50 kg: 1-2 g once a day (every 24 hours). In severe cases or for infections with pathogens that are only moderately sensitive to ceftriaxone, the daily dose can be increased to 4 g.
The duration of treatment depends on the course of the disease. As always with antibiotic therapy, Ceftriaxone-AKOS should be continued in patients for at least 48-72 hours after the temperature has returned to normal and confirmation of pathogen eradication.
Usually, the course of treatment is 4-14 days; for complicated infections, a longer use may be required. The course of treatment for Streptococcuspyogenes infections should be at least 10 days.
Introduction
The general rule should be to use solutions immediately after cooking.
The prepared solutions retain their physical and chemical stability for 6 hours at room temperature (or for 24 hours at a temperature of 2-8 °C). Depending on the concentration and duration of storage, the color of the solutions can vary from pale yellow to amber. The color of the solution does not affect the effectiveness or tolerability of the drug.
For intramuscular injection,500 mg of Ceftriaxone-AKOS is dissolved in 2 ml and 1 g-in 35 ml of 1% lidocaine solution and injected deep into a sufficiently large muscle (buttock). It is recommended to inject no more than 1 g into the same muscle.
A solution containing lidocaine should not be administered intravenously.
For intravenous injection,500 mg of Ceftriaxone-AKOS is dissolved in 5 ml and 1 g in 10 ml of sterile water for injection; it is administered intravenously slowly for 5 minutes, preferably into a large vein.
The intravenous infusion should last at least 30 minutes. To prepare the solution, dilute 2 g of Ceftriaxone-AKOS in 40 ml of one of the following infusion solutions that do not contain calcium ions: 09% sodium chloride solution 045% sodium chloride solution + 25% dextrose solution 5% dextrose solution 10% dextrose solution 6% dextran solution in 5% dextrose solution 6-10% hydroxyethyl starch solution water for injection. Solutions of Ceftriaxone-AKOS should not be mixed or added to solutions containing other antimicrobials or other solvents other than those listed above due to possible incompatibilities.
Do not use calcium-containing solvents such as Ringer’s solution or Hartmann’s solution for the preparation of solutions of Ceftriaxone-AKOS for intravenous use and their subsequent dilution, because of the possible formation of precipitates. The formation of ceftriaxone calcium salt precipitates can also occur when Ceftriaxone-AKOS is mixed with calcium-containing solutions using a single venous approach. Do not use ceftriaxone simultaneously with calcium – containing solutions for intravenous use, including long-term infusions of calcium-containing solutions, for example, with parenteral nutrition using a Y-connector. For all groups of patients except newborns, sequential use of Ceftriaxone – AKOS and calcium-containing solutions is possible, with careful flushing of the infusion systems between infusions with a compatible liquid (see the section “Interaction with other drugs”).
There have been no reports of interactions between ceftriaxone and oral calcium-containing drugs or interactions between ceftriaxone for intramuscular use and calcium-containing drugs (for intravenous or oral use).
Dosage in special cases
Patients with impaired liver function
In patients with impaired liver function, there is no need to reduce the dose, provided that there are no renal disorders.
Patients with impaired renal function
In patients with impaired renal function, there is no need to reduce the dose, provided that there are no violations of liver function. The daily dose of Ceftriaxone-ACOS should not exceed 2 g only in cases of renal insufficiency with a creatinine clearance of less than 10 ml / min. Ceftriaxone-AKOS is not excreted during hemodialysis or peritoneal dialysis, so an additional dose of Ceftriaxone-AKOS is not required after dialysis.
If a combination of severe renal and hepatic insufficiency occurs, you should carefully
monitor the effectiveness and safety of the drug.
Elderly and senile patients
Normal adult doses, not adjusted for age, provided there is no severe renal or hepatic insufficiency.
Children
Newborns children and children under 12 years of age
When prescribing Ceftriaxone-AKOS once a day, it is recommended to adhere to the following dosage regimens::
– newborn (up to 14 days): 20-50 mg/kg of body weight once a day; the daily dose should not exceed 50 mg/kg of body weight;
newborns – children and young children (from 15 days to 12 years): 20-80 mg/kg of body weight once a day;
– children with a body weight over 50 kg administered doses for adults.
Ceftriaxone is contraindicated in premature children under 41 weeks of age (total gestational and chronological age).
Ceftriaxone is contraindicated in newborns (≤28 days) who are already prescribed or are expected to receive intravenous treatment with calcium-containing solutions, including prolonged calcium-containing infusions, for example, with parenteral nutrition due to the risk of precipitation of ceftriaxone calcium salts (see section “Contraindications”).
In children and children under 12 years of age, intravenous doses of 50 mg / kg or higher should be administered dropwise for at least 30 minutes. In newborns, intravenous use should be performed within 60 minutes to reduce the potential risk of developing bilirubin encephalopathy.
Meningitis
In case of bacterial meningitis in children and young children, treatment begins with a dose of 100 mg / kg (but not more than 4 g) once a day. After identifying the pathogen and determining its sensitivity, the dose can be reduced accordingly.
The best results in meningococcal meningitis were achieved with a treatment duration of 4 days and meningitis caused by Haemophilus Influenzae-6 days Streptococcus Pneumoniae – 7 days.
Lyme
disease 50 mg / kg (highest daily dose – 2 g) for adults and children once a day for 14 days.
Gonorrhea caused by penicillinase-forming and penicillinase-forming strains).
A single intramuscular injection of 250 mg of Ceftriaxone-AKOS in adult patients and children over 12 years of age ≥50 kg.
Acute otitis media
In the treatment of acute otitis media in children, a single intramuscular injection at a dose of 50 mg/kg (but not more than 1 g) is recommended.
For adults, a single intramuscular dose of 1-2 g is recommended. According to limited data, in severe cases or if previous therapy is ineffective, Ceftriaxone-AKOS may be effective if administered intramuscularly at a dose of 1-2 g per day for 3 days.
Prevention of postoperative infections
Depending on the degree of infection risk,1-2 g of Ceftriaxone – AKOS is administered once 30-90 minutes before the operation. Simultaneous use of Ceftriaxone-AKOS and one of the 5 – nitroimidazoles, such as ornidazole, has proven to be effective in operations on the colon and rectum (but separately, see the section “Dosage and use”).
Overdose
Symptoms
Nausea, vomiting and diarrhea.
Treatment
In case of overdose, hemodialysis and peritoneal dialysis will not reduce the concentration of the drug. There is no specific antidote. Treatment of overdose is symptomatic.
Special instructions
Hypersensitivity reactions
As with other beta-lactam antibiotics, severe hypersensitivity reactions, including fatal ones, have been reported. If a severe hypersensitivity reaction develops, therapy with Ceftriaxone-AKOS should be immediately discontinued and appropriate urgent medical measures should be taken. Before starting therapy with Ceftriaxone-ACOS, it is necessary to determine whether the patient has experienced hypersensitivity reactions to ceftriaxone cephalosporins or severe hypersensitivity reactions to other beta-lactam antibiotics (penicillins, monobactams, and carbapenems).
Caution should be exercised when using ceftriaxone in patients with a history of mild hypersensitivity reactions to other beta-lactam antibiotics (penicillins, monobactams, and carbapenems).
Severe life-threatening or fatal skin hypersensitivity reactions (Stevens – Johnson syndrome or Lyell’s syndrome/toxic epidermal necrolysis) and drug reactions with eosinophilia and systemic symptoms (DRESS syndrome) have been reported. The frequency of such reactions is unknown.
Shortly after treatment with ceftriaxone, some patients with spirochete infection may experience a Jarisch-Herxheimer reaction (JHR). The reaction usually resolves on its own or can be stopped by symptomatic treatment.
If a reaction occurs, antibiotic treatment should not be discontinued.
Sodium content
1 g of Ceftriaxone-AKOS contains 36 mmol of sodium. This should be taken into account in patients on a sodium-controlled diet.
Hemolytic anemia
As with other cephalosporins, autoimmune hemolytic anemia may occur during treatment with Ceftriaxone-ACOS. Cases of severe hemolytic anemia in adults and children, including fatal cases, have been reported. If a patient undergoing treatment with ceftriaxone develops anemia, the diagnosis of cephalosporin-associated anemia cannot be excluded and treatment should be discontinued until the cause is determined.
Diarrhea caused by Clostridium Difficile
As with most other antibacterial agents, cases of Clostridium Difficile-induced diarrhea have been reported with ceftriaxone varying severity: from mild diarrhea to fatal colitis. Treatment with antibacterial drugs suppresses the normal microflora of the colon and provokes the growth of C. difficile. In turn, C. difficile forms toxins A and B, which are factors in the pathogenesis of diarrhea caused by C. difficile. Strains of C. difficile that produce hyper-toxins are infectious agents with a high risk of complications and mortality due to their possible resistance to antimicrobial therapy, while treatment may require colectomy. It is necessary to keep in mind the possibility of developing diarrhea caused by C. difficile in all patients with diarrhea after antibiotic therapy. A thorough medical history should be collected because cases of C. difficile-induced diarrhea have been reported more than 2 months after antibiotic therapy. If C. difficile-related diarrhea is suspected or confirmed, current non-C. difficile-directed antibiotic therapy may need to be discontinued. In accordance with the clinical indications, appropriate treatment should be prescribed with the introduction of fluids and electrolytes of proteins antibiotic therapy for C. difficile surgical treatment. Do not use medications that inhibit intestinal perilstatistics.
Superinfections
As with treatment with other antibacterial drugs, superinfections can develop.
Changes in prothrombin time
Rare cases of changes in prothrombin time have been reported in patients treated with Ceftriaxone-ACOS. Patients with vitamin K deficiency (impaired synthesis and nutrition) may need to monitor prothrombin time during therapy and be prescribed vitamin K (10 mg / week) if the prothrombin time is increased before or during therapy.
Formation of ceftriaxone calcium salt precipitates
Cases of fatal reactions resulting from the deposition of ceftriaxone-calcium precipitates in the lungs and kidneys of newborns are described. Theoretically, there is a possibility of interaction of ceftriaxone with calcium-containing solutions for intravenous use and in other age groups of patients, therefore, ceftriaxone should not be mixed with calcium-containing solutions (including for parenteral nutrition) and also administered simultaneously, including through separate accesses for infusions at different sites. Theoretically, based on the calculation of 5 half-lives of ceftriaxone, the interval between use of ceftriaxone and calcium-containing solutions should be at least 48 hours.
Data on the possible interaction of ceftriaxone with calcium-containing drugs for oral use and ceftriaxone for intramuscular use with calcium-containing drugs (intravenously or orally) are not available. After the use of ceftriaxone, usually in doses exceeding the standard recommended (1 g per day or more), ultrasound examination of the gallbladder revealed precipitation of ceftriaxone calcium salt, the formation of which is most likely in children. Precipitates rarely show any symptoms and disappear after completion or discontinuation of therapy with Ceftriaxone-AKOS. If these phenomena are accompanied by clinical symptoms, conservative non-surgical treatment is recommended, and the decision to discontinue the drug is left to the discretion of the attending physician and should be based on an individual assessment of the benefit and risk.
Despite the presence of data on the formation of intravascular precipitates only in newborns when using Ceftriaxone and calcium-containing infusion solutions of any other calcium-containing drugs. Ceftriaxone-AKOS should not be mixed or administered to children and adult patients simultaneously with calcium-containing infusion solutions, even using different venous approaches (see the sections “Contraindications” ” Interaction with other drugs “subsection” Post-marketing surveillance”).
Pancreatitis
Patients treated with Ceftriaxone-ACOS have been reported to have rare cases of pancreatitis that may have developed due to biliary tract obstruction. Most of these patients already had risk factors for biliary tract congestion such as previous therapy severe illnesses and full parenteral nutrition. At the same time, it is impossible to exclude the triggering role of biliary tract precipitates formed under the influence of Ceftriaxone-AKOS in the development of pancreatitis.
Use in children
The safety and efficacy of Ceftriaxone-AKOS in newborns, children and young children were determined for the dosages described in the section “Dosage and use”. Studies have shown that, like other cephalosporins, ceftriaxone can displace bilirubin from binding to serum albumin.
Ceftriaxone-AKOS should not be used in newborns, especially preterm infants, who are at risk of developing bilirubin encephalopathy (see the section “Contraindications”).
Long-term treatment
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.
Blood test monitoring
With long-term treatment, a complete blood test should be performed regularly.
Serological studies
When treated with ceftriaxone, false positive results of the Coombs test for galactosemia may be observed when determining glucose in the urine (glucosuria is recommended to be determined only by the enzyme method).
Influence on the ability to drive vehicles and mechanisms:
There are no data indicating the effect of the drug on driving vehicles and working with machines and mechanisms. However, during therapy with Ceftriaxone-ACOS, caution should be exercised when driving vehicles and working with mechanisms due to the possibility of dizziness and other adverse reactions that may affect the ability to drive vehicles with mechanisms.
Storage conditions
Store in a dark place at a temperature not exceeding 25 °C.
Keep out of reach of children.
Shelf
life is 3 years. Do not use after the expiration date.
Active ingredient
Ceftriaxone
Conditions of release from pharmacies
By prescription
Dosage form
solution for injection and infusion
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Side effects of Ceftriaxone-ACOS powder for intravenous and intramuscular injection solution 2g, 1pc
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