Metronidazole Tablets Bp 200mg
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
METRONIDAZOLE TABLETS BP 200mg
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains 200mg Metronidazole PhEur.
3 PHARMACEUTICAL FORM
White film-coated tablets.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
Metronidazole is active against a wide range of pathogenic micro-organisms, notably species of Bacteroids, Fusobacteria, Clostridia, Eubacteria, anaerobic cocci and Gardnerella vaginalis.
It is also active against Trichomonas vaginalis, Entamoeba histolytica, Gardia lamblia, Balantidium coli and Helicobacter pylori.
Metronidazole is indicated in adults and children for the following indications:
1) Prevention of post-operative infections due to anaerobic bacteria, particularly species of bacteroids and anaerobic streptococci.
2) The treatment of septicaemia, bacteraemia, peritonitis, brain abscess, necrotising pneumonia, osteomyelitis, puerperal sepsis, pelvic abscess, pelvic cellulitis and post-operative wound infections from which pathogenic anaerobes have been isolated.
3) Urogenital trichomoniasis in the female (Trichomonas vaginalis), and in man.
4) Bacterial vaginosis (also known as non-specific vaginitis, anaerobic vaginosis or Gardnerella vaginalis).
5) All forms of amoebiasis (intestinal and extra-intestinal disease and asymptomatic cyst passers).
6) Giardiasis.
7) Acute ulcerative gingivitis.
8) Acute dental infections (eg acute pericoronitis and acute apical infections)
9) Anaerobically-infected leg ulcers and pressure sores.
10) Treatment of Helicobacter pylori infection associated with peptic ulcer as part of triple therapy.
Consideration should be given to official guidance on the appropriate use of antibacterial agents.
4.2 Posology and method of administration
Posology
Metronidazole Tablets should be taken during or after meals, swallowed with water and NOT CHEWED.
Elderly: Caution is advised in the elderly, particularly at high doses, although there is limited information available on modification of dosage.
Hepatic impairment: Caution is advised in patients with hepatic encephalopathy. One third of the daily dose given once a day should be considered (see section 4.4).
1) Anaerobic infections:
Treatment for 7 days should be satisfactory for most patients but, depending upon clinical and bacteriological assessments, the physician may decide to prolong treatment, eg for eradication of infection from sites which cannot be drained or are liable to endogenous recontamination by anaerobic pathogens from the gut, oropharynx or genital tract.
Children > 8 weeks to 12 years of age: The usual daily dose is 20-30 mg/kg/day as a single dose or divided into 7.5 mg/kg every 8 hours. The daily dose may be increased to 40 mg/kg, depending on the severity of the infection. Duration of treatment is usually 7 days.
Children < 8 weeks of age: 15 mg/kg as a single dose daily or divided into 7.5 mg/kg every 12 hours.
In newborns with a gestation age <40 weeks, accumulation of metronidazole can occur during the first week of life, why the concentrations of metronidazole in serum should preferable be monitored after a few days therapy.
Children under 10 years: A more suitable dosage form should be used for this age group.
Prophylaxis against anaerobic infection - chiefly in the context of abdominal (especially colorectal) and gynaecological surgery.
Adults: 1g stat dose 24 hours pre-operatively, followed by 400mg at 8 hourly intervals during the 24 hours preceding operation followed by post-operative iv or rectal administration until the patient is able to take tablets.
Children < 12years: 20-30 mg/kg as a single dose given 1-2 hours before surgery.
Newborns with a gestation age <40 weeks: 10 mg/kg body weight as a single dose before operation.
Children under 10 years: A more suitable dosage form should be used for this age group.
2) Treatment of established infections:
Adults and children over 10 years: 800mg followed by 400mg 8 hourly.
Children under 10 years: A more suitable dosage form should be used for this age group.
3) Urogenital trichomoniasis: Where reinfection is likely, sexual partners should be treated concomitantly.
Adults and adolescents: 2000 mg as a single dose or 200 mg 3 times daily for 7 days or 400 mg twice daily for 5-7 days.
Children < 10years: 40 mg/kg orally as a single dose or 15 - 30 mg/kg/day divided in 2-3 doses for 7 days; not to exceed 2000 mg/dose.
Children under 10 years: A more suitable dosage form should be used for this age group.
4) Bacterial vaginosis
Adults: 400mg twice daily for 7 days, or 2g as a single dose for one day only. Adolescents: 400 mg twice daily for 5-7 days or 2000 mg as a single dose.
5) Amoebiasis
Adults> 10 years: 400 to 800 mg 3 times daily for 5-10 days.
Children 7 to 10years: 200 to 400 mg 3 times daily for 5-10 days.
Children 3 to 7years: 100 to 200 mg 4 times daily for 5-10 days.
Children 1 to 3 years: 100 to 200 mg 3 times daily for 5-10 days.
Alternatively, doses may be expressed by body weight:
35 to 50 mg/kg daily in 3 divided doses for 5 to 10 days, not to exceed 2400 mg/day.
Children under 7 years: A more suitable dosage form should be used for this age group.
6) Giardiasis:
Adults > 10 years: 2000 mg once daily for 3 days, or 400 mg. three times daily for 5 days, or 500 mg twice daily for 7 to 10 days.
Children 7 to 10 years: 1000 mg once daily for 3 days.
Children 3 to 7years: 600 to 800 mg once daily for 3 days.
Children 1 to 3 years: 500 mg once daily for 3 days.
Alternatively, as expressed in mg per kg of body weight:
15-40 mg/kg/day divided in 2-3 doses.
Children under 7 years: A more suitable dosage form should be used for this age group.
7) Acute ulcerative gingivitis (for 3 day duration):
Adults and children over 10 years: 200mg three times daily.
Children under 10 years: A more suitable dosage form should be used for this age.
8) Acute dental infections (for 3-7 day duration):
Adults and children over 10 years: 200mg three times daily.
9) Leg ulcers and pressure sores (for 7 day duration):
Adults and children over 10 years: 400mg three times daily.
10) Treatment of Helicobacter pylori in infected patients
As a part of a combination therapy, 20 mg/kg/day not to exceed 500 mg twice daily for 7-14 days. Official guidelines should be consulted before initiating therapy.
Method of Administration For oral administration.
4.3 Contraindications
• Known hypersensitivity to metronidazole or any of the ingredients in the tablets.
• Pregnancy - metronidazole should not be used in the first trimester in patients with trichomoniasis or bacterial vaginosis (see section 4.6).
• Breast feeding should be discontinued for 12-24 hours when single high dose (e.g. 2g) therapy is used (see section 4.6).
4.4 Special warnings and precautions for use
• Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take metronidazole as this product contains lactose.
• Patients should abstain from alcohol for at least 48 hours following discontinuation of therapy with metronidazole. A disulfiram-like reaction with hypotension and flushing has occurred (see section 4.5).
• Caution is advised in patients with porphyria.
• Metronidazole tablets should not be used in patients with blood dyscrasias or with active non-infectious disease of the central nervous system. High doses of metronidazole may mask the presence of syphilis.
• Caution in patients with epilepsy or those who have had seizures as high doses of Metronidazole can induce seizures.
• Use with caution in the second and third trimester when used to treat trichomoniais or bacterial vaginosis (see section 4.6.)
• Regular clinical and laboratory surveillance are advised if treatment continues for more than 10 days.
• Consideration of the therapeutic benefit against the risk of peripheral neuropathy is advised with continuous therapy for chronic conditions.
• There is a possibility that after Trichomonas vaginalis has been eliminated a gonococcal infection might persist.
• The elimination half-life of metronidazole remains unchanged in the presence of renal failure. The dosage of metronidazole, therefore, needs no reduction. Such patients, however, retain the metabolites of metronidazole. The clinical significance of this is not known at present.
• In patients undergoing haemodialysis metronidazole and metabolites are efficiently removed during an eight-hour period of dialysis. Metronidazole should, therefore, be readministered immediately after haemodialysis.
• No routine adjustment in the dosage of metronidazole need be made in patients with renal failure undergoing intermittent peritoneal dialysis (IPD) or continuous ambulatory peritoneal dialysis (CAPD).
• Metronidazole is mainly metabolised by hepatic oxidation. Substantial impairment of metronidazole clearance may occur in the presence of advanced hepatic insufficiency. Signficant cumulation may occur in patients with hepatic encephalopathy and the resulting high plasma concentrations of metronidazole may contribute to symptoms of the encephalopathy. Therefore, metronidazole should be administered with caution to patients with hepatic encephalopathy.
The daily dosage should be reduced to one third and may be administered once daily.
4.5 Interaction with other medicinal products and other forms of interaction
• Interactions to be used with caution:
■ Lithium: Lithium retention accompanied by evidence of possible renal damage has been reported in patients treated simultaneously with lithium and metronidazole. Lithium treatment should be tapered or withdrawn before administering metronidazole. Plasma concentration of lithium, creatinine, and electrolytes should be monitored in patients under treatment with lithium while they receive metronidazole.
■ Anticoagulants: Some potentiation of anticoagulant therapy has been reported when metronidazole has been used with the warfarin type oral anticoagulants. Dosage of the latter may require reducing. Prothrombin times should be monitored. No interactions have been reported with anticoagulants of the heparin type. However, anticoagulant activity should be routinely monitored with these products.
■ Alcohol: Patients should be advised not to take alcohol during metronidazole therapy and for at least 48 hours after because of the possibility of a disulfiram-like reaction.
■ Disulfiram: Psychotic reactions have been reported.
■ Immunosuppressants: Patients receiving ciclosporin are at risk of elevated ciclosporin serum levels. Serum ciclosporin and serum creatinine should be closely monitored when coadministration is necessary.
• Pharmacokinetic interactions:
■ Antiepileptics: Patients receiving phenobarbital metabolise metronidazole at a much greater rate than normally, reducing the half-life to approximately 3 hours. Metronidazole inhibits metabolism of phenytoin (increases plasma-phenytoin concentration). Primidone accelerates the metabolism of Metronidazole causing reduced plasma concentrations.
■ Cytotoxics: Metronidazole inhibits metabolism of fluorouracil. Therefore, increased toxicity of fluorouracil can result.
■ Ulcer-healing drugs: Cimetidine inhibits the metabolism of metronidazole (increases plasma-metronidazole concentration).
■ Oestrogens: broad spectrum antibiotics possibly reduce the contraceptive effect. See local/national guidelines or BNF for specific advice.
Drug-lab modifications: Aspartate amino transferase assays may give spuriously low values in patients taking metronidazole, depending on the method used.
4.6 Pregnancy and lactation
As with all medicines, metronidazole should not be given during pregnancy or during lactation unless it is considered essential, and in these circumstances the short, high-dosage regimens are not recommended.
Metronidazole is contraindicated in the first trimester (see section 4.3) and should be used with caution in the second and third trimester when used to treat trichomoniais or bacterial vaginosis (see section 4.4).
For all other indications Metronidazole should only be used if the benefits outweight the risks or no other alternative is available especially in the first trimester.
It is advisable to stop breast feeding until 12 - 24 hours after Metronidazole therapy has been discontinued when single high doses have been used (see section 4.3).
4.7 Effects on ability to drive and use machines
Patients should be warned about the potential for drowsiness, dizziness, confusion, hallucinations, convulsions or transient visual disorders, and advised not to drive or operate machinery if these symptoms occur.
4.8 Undesirable effects
Frequency type and severity of adverse reactions in children are the same as in adults
The frequency of adverse events listed below is defined using 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).
Serious adverse reactions occur rarely with standard recommended regimens. Clinicians who contemplate continuous therapy for the relief of chronic conditions, for periods longer than those recommended, are advised to consider the possible therapeutic benefit against the risk of peripheral neuropathy.
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Blood and lymphatic system disorders: | |
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Very rare |
agranulocytosis, neutropenia, thrombocytopenia, pancytopenia |
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Not known |
Leucopenia, bone marrow depression disorders such as aplastic anaemia |
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Immune system class: |
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Rare |
anaphylaxis |
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Not known |
angiodema, urticaria, fever |
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Metabolism and nutrition disorders: | |
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Not known |
anorexia |
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Psychiatric disorders: | |
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Very rare |
Psychotic disorders, including hallucinations |
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Nervous system disorders; | |
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Very rare |
• Encephalopathy (eg. Confusion, fever, headache, paralysis, light sensitivity, disturbances in sight and movement, stiff neck) and subacute cerebellar syndrome (eg. Ataxia, dysathria, gait impairment, nystagmus and tremor) which may resolve in discontinuation of the drug. • Drowsiness, dizziness, convulsions, headaches |
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Not known |
Depression, paraesthesia, during intensive and-or prolonged metronidazole therapy, peripheral sensory neuropathy or transient epileptiform seizures have been reported. In most cases neuropathy disappeared after treatment was stopped or when dosage was reduced. Incoordination of movement |
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Eye disorders: | |
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Very rare |
diplopia, myopia |
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Gastrointestinal disorders: | |
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Not known |
unpleasant taste in the mouth, taste disorders, oral mucositis, furred tongue, nausea, vomiting, gastrointestinal disturbances, diarrhoea, abdominal pain, anorexia |
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Hepatobiliary disorders: | |
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Very rare |
abnormal liver function tests, cholestatic hepatitis, jaundice and pancreatitis which is reversible on drug withdrawal |
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Skin and subcutaneous tissue disorders: | |
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Very rare |
skin rashes, pustular eruptions, pruritis, flushing |
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Not known |
erythema multiforme |
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Musculoskeletal, connective tissue and bone disorders: | |
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Very rare |
myalgia, arthralgia |
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Renal and urinary disorders: |
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Very rare |
Darkening of urine (due to |
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metronidazole metabolite) |
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation 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 via the Yellow Card Scheme; website: www.mhra.gov.uk/yellowcard
4.9 Overdose
Features:
Nausea, vomiting, diarrhoea, anorexia, metallic taste, headache, dizziness and occasionally insomnia and drowsiness. Transiently increased liver enzyme activities have been reported rarely.
Transient epileptiform seizures have been reported following intensive or prolonged therapy. Other adverse effects occurring in these circumstances include peripheral motor neuropathy, blood dyscrasias and liver damage.
The combination of alcohol and metronidazole has been said to cause disulfiram type reactions in about 10% of individuals with sudden onset of excitement, giddiness, flushing, nausea, headache, hypotension and dyspnoea. However the mechanism of this reaction has been questioned.
Treatment:
Unlikely to be required.
Disulfiram type reactions should be treated with intravenous fluids and plasma expanders if necessary. Symptomatic and supportive.
In more serious cases:
1. Single brief convulsions do not require treatment. If frequent or prolonged control with intravenous diazepam (10-20mg in adults; 0.1-0.3mg/kg body weight) or lorazepam (4mg in an adult and 0.05mg/kg in a child). Give oxygen and correct acid base and metabolic disturbances as required.
2. Other measures as indicated by the patient's clinical condition.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
ATC Code: P01A B01
Metronidazole has antiprotozoan and antibacterial effects. It is effects against Trichomonas vaginalis, Gardnerella vaginalis and other protazoa including Entamoeba histolytica, Gardia lamblia and anaerobic bacteria.
5.2 Pharmacokinetic properties
Absorption - Metronidazole is readily absorbed following administration by mouth and bioavailability is 90-100%. Peak plasma concentrations of approximately 5pg/ml and 10pg/ml are achieved an average of 1-2 hours after single doses of 250mg and 500mg respectively. Some accumulation and consequently higher concentrations occur when multiple doses are given. Absorption may be delayed, but is not reduced overall, by administration with food.
Distribution - Metronidazole is widely distributed. It appears in most body tissues and fluids. It also crosses the placenta and rapidly enters foetal circulation. No more than 20% is bound to plasma proteins.
Metabolism - Metronidazole is metabolised in the liver by side-chain oxidation and glucuronide formation. The plasma elimination half-life of metronidazole is about 69 hours; that of the hydroxy metabolite is slightly longer. The half-life of metronidazole is reported to be longer in neonates and in patients with severe liver disease.
Elimination - The majority of a dose of metronidazole is excreted in the urine, mainly as metabolites; a small amount appears in the faeces.
5.3 Preclinical safety data
Not applicable.
6 PHARMACEUTICAL PARTICULARS
6.1 List of excipients
Also contains: carmellose sodium, cellulose, colloidal silica, lactose, magnesium stearate, maize starch, polyethylene glycol, titanium dioxide (E171), hydroxypropylcellulose (E463), methylhydroxypropylcellulose (E464), water.
6.2 Incompatibilities
None known.
6.3 Shelf life
Shelf-life
Three years from the date of manufacture.
Shelf-life after dilution/reconstitution Not applicable.
Shelf-life after first opening Not applicable.
6.4 Special precautions for storage
Store below 25°C in a dry place.
6.5 Nature and contents of container
The product containers are rigid injection moulded polypropylene or injection blow-moulded polyethylene containers and snap-on polyethylene lids; in case any supply difficulties should arise the alternative is amber glass bottles with screw caps. An alternative closure for polyethylene containers is a polypropylene, twist on, push down and twist off child-resistant, tamper-evident lid.
The product may also be supplied in blister packs in cartons:
a) Carton: Printed carton manufactured from white folding box board.
b) Blister pack: (i) 250pm white rigid PVC. (ii) Surface printed 20pm hard temper aluminium foil with 5-7g/M2 PVC and PVdC compatible heat seal lacquer on the reverse side.
Pack size: 14s, 20s, 21s, 28s, 30s, 50s, 56s, 60s, 84s, 90s, 100s, 112s, 120s, 168s, 180s, 250s, 500s, 1000s.
Product may also be supplied in bulk packs, for reassembly purposes only, in polybags contained in tins, skillets or polybuckets filled with suitable cushioning material. Bulk packs are included for temporary storage of the finished product before final packaging into the proposed marketing containers.
Maximum size of bulk packs: 25,000.
6.6 Special precautions for disposal
Not applicable.
7 MARKETING AUTHORISATION HOLDER
Actavis UK Limited (Trading style: Actavis)
Whiddon Valley Barnstaple North Devon EX32 8NS
8 MARKETING AUTHORISATION NUMBER(S)
PL 0142/0250
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE
AUTHORISATION
12/06/1987 / 22/10/2004
10 DATE OF REVISION OF THE TEXT
05/12/2014