Kemicetine Injection
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Kemicetine Injection
Chloramphenicol 1 g Powder for Injection
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each vial contains 1.377 g of chloramphenicol sodium succinate (equivalent to 1.0g of laevorotatory chloramphenicol)
Each vial contains 71.2 mg sodium.
3 PHARMACEUTICAL FORM
Powder for solution for injection (Powder for Injection).
Freeze dried powder, pale yellowish porous mass.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Chloramphenicol is indicated for typhoid, meningitis caused by H. influenzae and other serious infections caused by bacteria susceptible to chloramphenicol.
It is also indicated wherever chloramphenicol is deemed the antibiotic of choice and oral administration is not possible, or where higher than usual blood concentrations are required.
4.2 Posology and method of administration
Posology
The dose administered and the concentration used is dependent on the severity of the infection. The recommended standard dosage is as follows:
Adults : The equivalent of 1 g of chloramphenicol every 6-8 hours.
Elderly : The usual adult dosage should be given subject to normal hepatic and renal function.
Children : The equivalent of 50 mg/kg chloramphenicol according to body weight, daily in divided doses every 6 hours (this dose should not be exceeded). The patient should be carefully observed for signs of toxicity.
Neonates and Premature Infants : 25 mg/kg in divided doses.
Only 10% or lower concentrations to be used. The 10% solution can be prepared by extracting 5ml of the 20% solution and adding 5ml of diluent (Water for Injections, Sodium Chloride Injection or Dextrose Injection 5%) under aseptic conditions.
The 10 % solution should be given by intravenous injection over a period of about a minute, or in a larger volume of fluid, by slow intravenous infusion. The concurrent administration of intravenous Chloramphenicol with topical treatment has been found to be very effective in the treatment of osteomyelitic foci, abscesses, empyema and skin and urinary infections.
In exceptional cases, such as patients with septicaemia or meningitis, dosage schedule up to 100 mg/kg/day may be prescribed. However, these high doses should be decreased as soon as clinically indicated. To prevent relapses treatment should be continued after the temperature has returned to normal for 4 days in rickettsial diseases and for 8 - 10 days in typhoid fever.
Method of administration
To be given by intravenous or intramuscular injection.
In order to ensure rapid attainment of high blood levels, Chloramphenicol is best administered by intravenous injection. Where this is not possible, however, intramuscular administration may be used, although it should be borne in mind that absorption may be slow and unpredictable.
The injection should be reconstituted with Water for Injections, Sodium Chloride Injection, or Dextrose Injection 5 %. The following dilution table may be useful for the administration of a proportion of the contents of a vial:
|
Concentration |
Solution strength |
Volume of diluent to be added |
Total volume after dilution |
|
40% |
400 mg/ml |
1.7 ml |
2.5 ml |
|
25% |
250 mg/ml |
3.2 ml |
4.0 ml |
|
20% |
200 mg/ml |
4.2 ml |
5.0 ml |
4.3 Contraindications
Chloramphenicol is contraindicated in patients with a previous history of sensitivity and/or toxic reaction to chloramphenicol.
4.4 Special warnings and precautions for use
Chloramphenicol is to be administered only under the direction of a medical practitioner. It should be reserved for serious infections caused by organisms susceptible to its antimicrobial effects when less toxic antibiotics are ineffective or contraindicated. However, chloramphenicol may be chosen to initiate antibiotic therapy based on the clinical impression. In vitro sensitivity tests should be performed concurrently so that the drug may be discontinued as soon as possible if a less toxic antibiotic is indicated by the results of such tests. The decision to continue use of chloramphenicol, rather than another antibiotic when both are suggested by in vitro studies to be effective against a specific pathogen, should be based upon severity of the infection, susceptibility of the pathogen to the various antimicrobial drugs, and the efficacy of the various drugs in the infection.
Chloramphenicol should not be used for trivial infections due to the possibility of severe blood dyscrasias, which may prove fatal.
Bone marrow depression and blood disorders
Serious and fatal blood dyscrasias (aplastic anaemia, hypoplastic anaemia, thrombocytopenia, granulocytopenia, and bone marrow depression) are known to occur after the administration of chloramphenicol. (See section 4.8) In addition, there have been reports of aplastic anaemia attributed to chloramphenicol, which later resulted in leukaemia. Blood dyscrasias have occurred after both short-term and prolonged therapy with this drug. Chloramphenicol must not be used in the treatment of any infection for which a less toxic antibiotic is available (see section 4.1).
Patient monitoring
Because of its toxic nature it is important to monitor serum levels of this antibiotic particularly in new-born and premature infants, in the elderly, in patients with renal or hepatic disease and in those receiving other drugs with which chloramphenicol may interact (see section 4.5).
It is essential that adequate haematologic functions be closely monitored during treatment with chloramphenicol. While haematologic determinations may detect early peripheral haematologic changes, such as leucopoenia, reticulocytopenia, or granulocytopenia, before they become irreversible, such determinations cannot be relied on to detect bone marrow depression prior to the development of aplastic anaemia.
It is desirable that patients be hospitalized during therapy, so that appropriate laboratory determinations and clinical observations can be made.
Baseline haematologic determinations should be made and determinations repeated approximately every two days during therapy. The drug should be discontinued upon appearance of reticulocytopenia, leucopoenia, thrombocytopenia, anaemia, or any other haematologic findings attributable to chloramphenicol. However, such determinations do not exclude the possible later appearance of the irreversible type of bone marrow depression.
Repeated courses of the drug should be avoided if at all possible. Treatment should not be continued longer than required to produce a cure with little or no risk of relapse of the disease. Concurrent therapy with other drugs that may cause bone marrow depression should be avoided.
Hepatic or Renal Impairment
Excessive chloramphenicol serum levels may result from administration of the recommended dose to patients with impaired liver or kidney function, including that due to immature metabolic processes in the infant. Dosage should be adjusted accordingly or, preferably, the serum concentration should be determined at appropriate intervals. (See section 4.2).
Grey syndrome in infants and neonates
Precaution should be used in therapy of premature and full-term neonates to avoid "Grey Syndrome" toxicity. Serum drug levels should be carefully monitored during therapy of the neonate (newborn infant).
Toxic reactions, including fatalities, have occurred in premature infants and neonates. The signs and symptoms associated with these reactions have been referred to as the "Grey Syndrome". Although "Grey Syndrome" has been reported in neonates born to mothers after having received chloramphenicol during labour, in most cases therapy with chloramphenicol has been instituted within the first 48 hours of life. The following summarizes the clinical and laboratory determinations that have been made on these patients. Symptoms first appeared after 3 to 4 days of continued treatment with high doses of chloramphenicol. The symptoms appeared in the following order: abdominal distension with or without emesis, progressive pallid cyanosis, vasomotor collapse, frequently accompanied by irregular respiration, death within a few hours of onset of these symptoms.
The progression of symptoms from onset to death was accelerated with higher dose schedules. Serum drug levels revealed unusually high concentrations of chloramphenicol (over 90 mcg/mL after repeated doses).
Termination of therapy upon early evidence of the associated symptomatology frequently reversed the process with complete recovery following.
General
Chloramphenicol must not be used in the treatment of trivial infections or where it is not indicated, as in colds, viral influenza, infections of the throat or as a prophylactic agent to prevent bacterial infections.
Superinfections
The use of chloramphenicol, as with other antibiotics, may result in an overgrowth of nonsusceptible organisms, including fungi. If infections caused by nonsusceptible organisms appear during therapy, appropriate measures should be taken.
Clostridium difficile associated diarrhoea (CDAD) has been reported with use of nearly all antibacterial agents, including chloramphenicol, and may range in severity from mild diarrhoea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C difficile.
C. difficile produces toxins A and B which contribute to the development of CDAD.
Hypertoxin producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhoea following antibiotic use. Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents.
Effects on immunity
Chloramphenicol may also impede the development of immunity and should therefore not be given during active immunisation.
4.5 Interaction with other medicinal products and other forms of interaction
Chloramphenicol has been shown to interact with, and enhance the effects of coumarin anticoagulants, some hypoglycaemic agents (e.g. tolbutamide) and phenytoin. When given concurrently, a dose reduction of these agents may be necessary.
Plasma concentrations of chloramphenicol may be reduced with concomitant usage of phenobarbital and rifampicin
4.6 Pregnancy and lactation
The use of chloramphenicol is contraindicated in pregnancy and whilst breastfeeding
4.7 Effects on ability to drive and use machines
None stated.
4.8 Undesirable effects
Tabulated summary of adverse reactions
The adverse reactions are grouped according to their system organ classes and the frequencies ranked according to the following convention: Very common (>1/10); Common (>1/100 to <1/10); Uncommon (>1/1,000 to <1/100); Rare (>1/10,000 to <1/1,000); Very rare (<1/10,000); Not known (cannot be estimated from the available data).
|
System Organ |
Very |
Common |
Uncommon |
Rare |
Very rare |
Not known (cannot |
|
Class |
common |
(>1/100 to |
(>1/1,000 to |
(>1/10,000 |
(<1/10,000) |
be estimated from the available data) |
|
(>1/10) |
<1/10) |
<1/100) |
to <1/1,000) | |||
|
Infections and infestations |
Fungal superinfection | |||||
|
Blood and lymphatic system disorders |
Aplastic anaemia |
Agranulocytosis Bone marrow failure Pancytopenia Thrombocytopenic purpura | ||||
|
Psychiatric disorders |
Depression | |||||
|
Nervous system disorders |
Peripheral neuritis Headache | |||||
|
Eye disorders |
Optic neuritis Transient blindness Blurred vision | |||||
|
Cardiac disorders |
Neonatal Grey syndrome | |||||
|
Gastrointestinal disorders |
Vomiting Diarrhoea Nausea Dry mouth | |||||
|
Skin and subcutaneous tissue disorders |
Urticaria |
Bone marrow depression and blood disorders
Chloramphenicol may cause severe bone marrow depression which may lead to serious and potentially fatal blood dyscrasias, such as agranulocytosis, thrombocytopenic purpura or aplastic anaemia (see section 4.4).
Paediatric population
Grey syndrome is a serious adverse effect that has been reported in neonates and infants following the intravenous administration of chloramphenicol (see section 4.4).
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorization of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions to:
United Kingdom Yellow card system www.mhra.gov.uk/yellowcard
4.9 Overdose
Levels exceeding 25 mcg/ml are frequently considered toxic.
Chloramphenicol toxicity can be evidenced by serious haemopoietic effects such as aplastic anaemia, thrombocytopenia, leucopenia, as well as increasing serum iron levels, nausea, vomiting and diarrhoea.
In the case of serious overdosage, charcoal haemoperfusion may be effective in removing chloramphenicol from plasma.
Exchange transfusion is of questionable value following massive overdosage, especially in neonates and infants.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
After administration chloramphenicol is rapidly released from chloramphenicol sodium succinate. Chloramphenicol is active against many gram-positive and gram negative organisms, Spirillae and Rickettsia. It acts by interfering with bacterial protein synthesis. Chloramphenicol is widely distributed in body tissues and fluids and enters the cerebrospinal fluid.
Chloramphenicol sodium succinate, free chloramphenicol and metabolites are excreted in the urine.
5.2 Pharmacokinetic properties
Absorption
After intravenous administration steady state peak concentrations were reached on average 18.0 minutes after cessation of the infusion.
Distribution
Chloramphenicol is widely distributed in body tissues and fluids and enters the cerebrospinal fluid.
Biotransformation
After administration chloramphenicol is rapidly released from chloramphenicol sodium succinate. Chloramphenicol sodium succinate, free chloramphenicol and metabolites are excreted in the urine.
Elimination
After intravenous administration of chloramphenicol succinate every 6 hours, the elimination half-lives were 4.03 hours for chloramphenicol and 2.65 hours for chloramphenicol succinate.
Paediatric population
In infants and children aged 3 days to 16 years the apparent half-life was extremely variable ranging from 1.7 to 12.0 hours
5.3 Preclinical safety data
None stated.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
None
6.2 Incompatibilities
None stated.
6.3 Shelf life
48 months.
6.4 Special precautions for storage
Keep container in the outer carton.
6.5 Nature and contents of container
Type III colourless glass vials with grey chlorobutyl rubber bung and aluminium seal.
Pack size: 1, 20 or 25 vials
6.6 Special precautions for disposal
To be reconstituted with Water for Injections, Sodium Chloride Injection or Dextrose Injection 5%.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements
MARKETING AUTHORISATION HOLDER
7
Essential Pharma Ltd 7 Egham Business Village Crabtree Road Egham, Surrey TW20 8RB United Kingdom
8 MARKETING AUTHORISATION NUMBER(S)
PL 41871/0015
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
02/03/2009
10 DATE OF REVISION OF THE TEXT
14/10/2016