1. Name Of The Medicinal Product
Trimethoprim 200mg Tablets
2. Qualitative And Quantitative Composition
Each tablet contains Trimethoprim 200mg
For a full list of excipients see section 6.1.
3. Pharmaceutical Form
Tablet: White coloured flat bevelled edged tablets engraved with 'MT200'.
Slight characteristic odour.
4. Clinical Particulars
4.1 Therapeutic Indications
Treatment of susceptible infections caused by trimethoprim sensitive organisms including most gram-positive and gram-negative aerobic organisms, including Haemophilus influenzae, Streptococcus pneumoniae, Klebsiella pneumonia, Staphylococcus aureus, Eschersichia coli, Enterobacter, Proteus and Streptococcus faecalis.
Exceptions include anaerobic bacteria. Mycobacterium tuberculosis, neisseria gonorrhoeae, pseudomonas aeruginosa and treponema pallidum.
Prophylaxis of recurrent urinary tract infections.
Consideration should be given to official guidance on the appropriate use of antibacterial agents
4.2 Posology And Method Of Administration
Posology
Acute infections:
Treatment should continue for a period of between three days (e.g. uncomplicated bacterial cystitis in women) and two weeks according to the nature and severity of infection. The first dose can be doubled.
• Adults and children over 12 years: 200mg twice daily.
• Children 6-12 years: 100mg twice daily.
• Children under 6 years of age: Not recommended; a more suitable dosage form should be used in this age group.
• Elderly: Dosage is dependent upon kidney function; see special dosage schedule.
Long-term treatment and prophylactic therapy:
• Adults and children over 12 years: 100mg at night.
• Children 6-12 years: 50mg at night. Where a single daily dose is required, dosage at bedtime may maximise urinary concentrations. The approximate dosage in children is 2mg trimethoprim per kg body weight per day.
• Elderly: Dosage is dependent upon kidney function; see special dosage schedule
Advised dosage schedule where there is reduced kidney function:
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Trimethoprim is removed by dialysis. However, it should not be administered to dialysis patients unless plasma concentrations can be estimated regularly.
Route of administration: oral
4.3 Contraindications
Hypersensitivity to trimethoprim or any of the excipients. Pregnancy. Severe hepatic insufficiency. Severe renal insufficiency where blood levels cannot be regularly monitored. Megaloblastic anaemia and other blood dyscrasias.Trimethoprim should not be administered to premature infants or children under 4 months of age.
4.4 Special Warnings And Precautions For Use
Administer with care to patients with impaired renal function. Regular haematological examination should be performed during long-term therapy.
Caution should be exercised in the administration of trimethoprim to patients with actual or potential folate deficiency (e.g. the elderly) and administration of folate supplement should be considered.
Although an effect on folate metabolism is possible, interference with haematopoiesis rarely occurs at the recommended dose. If any such change is seen, folinic acid should reverse the effect. Elderly people may be more susceptible and a lower dose may be advisable.
In patients with renal impairment, care should be taken to avoid accumulation.
Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorbtion should not take this medicine.
4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction
Special care is necessary patients receiving pyrimethamine therapy in addition to trimethoprim. Increased antifolate effect when trimethoprim is given with pyrimetamine.
Bone marrow depressants - trimethoprim may increase the potential for bone marrow aplasia.
Rifampicin may increase the elimination and shorten the elimination half-life of trimethoprim.
Phenytoin and digoxin - the patient should be carefully controlled as trimethoprim may increase the elimination half-life of phenytoin and digoxin.
Trimethoprim may potentiate the anticoagulant effect of warfarin
Ciclosporin may increase the nephrotoxicity of trimethoprim.
4.6 Pregnancy And Lactation
Trimethoprim is contraindicated during pregnancy (see section 4.3).
Although trimethoprim is excreted in breast milk, it is not necessarily contraindicated for short-term therapy during lactation.
4.7 Effects On Ability To Drive And Use Machines
None known
4.8 Undesirable Effects
Blood and lymphatic system disorders
Trimethoprim therapy may affect haematopoiesis
Immune system disorders
Photosensitivity and allergic reactions including urticaria, angioedema and anaphylaxis
Nervous system disorders
Headache, Aseptic meningitis
Gastrointestinal disorders
Gastro-intestinal disturbances including nausea and vomiting
Skin and subcutaneous tissue disorders
Pruritis, skin rashes.
More severe skin sensitivity reactions such as erythema multiforme, Stevens-Johnson Syndrome and ToxicEpidermal Necrolysis have been reported rarely.
Musculoskeletal and connective tissue disorders
Myalgia
4.9 Overdose
Treat symptomatically, gastric lavage and forced diuresis may be used. Depression of haematopoiesis by trimethoprim may be countered by intramuscular injections of calcium folinate.
5. Pharmacological Properties
5.1 Pharmacodynamic Properties
Pharmacotherapeutic Group: Systemic antibacterial. ATC Code: J01EA01
Mechanism of action: Trimethoprim is a dihydrofolate reductase inhibitor which affects the nucleoprotein metabolism of micro-organisms by interference in the folic-folinic acid systems.
Trimethoprim is effective in vitro against a wide range of Gram-positive and aerobic Gram-negative organisms, including enterobacteria Escherica coli, Proteus, Klebsiella pneumoniae, Streptococcus pneumoniae, Streptococcus faecalis, Haemophilus influenzae and Staphylococcus aureus.
It is not effective against Anaerobes, Pseudomonas aeruginosa, Treponema pallidum, Mycobacteria, Nocardia species, Neisseria species and Brucella abortus.
5.2 Pharmacokinetic Properties
Trimethoprim is rapidly and almost completely absorbed from the gastrointestinal tract and peak concentrations in the circulation occur about 1-4 hours after an oral dose. Peak plasma concentrations of about 1μg/ml have been reported after a single dose of 100mg. Approximately 40-70% is bound to plasma proteins. The half life is approximately 8-10 hours. About 40-60% of a dose is excreted unchanged in the urine within 24 hours, together with metabolites; hence, patients with impairment of renal function such as the elderly may require a reduction in dosage due to accumulation. It appears in breast milk.
5.3 Preclinical Safety Data
There is no pre-clinical data of relevance to the prescriber additional to that included in other sections of the SmPC.
6. Pharmaceutical Particulars
6.1 List Of Excipients
Lactose
Povidone 25cps
Crospovidone
Sodium starch glycollate
Magnesium stearate
6.2 Incompatibilities
None known
6.3 Shelf Life
36 months
6.4 Special Precautions For Storage
Do not store above 25°C. Store in the original container.
6.5 Nature And Contents Of Container
High density polystyrene with polythene lids and/or polypropylene containers with polythene lids and polyurethane or polythene inserts.
Blister pack - 25 micron PVC glass-clear/bluish rigid PVC (pharmaceutical grade) 20 micron hard-tempered aluminium foil coated on the pull side with 6-7gsm heat seal lacquer and printed on the bright side.
Pack sizes: 50, 100, 500, 1000, 5000 (Bulk pack), 6, 14 & 28 (blister pack)
Not all pack sizes may be marketed.
6.6 Special Precautions For Disposal And Other Handling
No special requirements
7. Marketing Authorisation Holder
Milpharm Limited,
Ares,
Odyssey Business Park,
West End Road,
South Ruislip HA4 6QD,
United Kingdom
8. Marketing Authorisation Number(S)
PL 16363/0024
9. Date Of First Authorisation/Renewal Of The Authorisation
8 March 2001
10. Date Of Revision Of The Text
01/11/2011
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