Type 2 diabetes mellitus [monotherapy or in combination
with other antidiabetic drugs (including insulin)]
▶BY MOUTH USING IMMEDIATE-RELEASE MEDICINES
▶Child 10–17 years (specialist use only): Initially 500 mg
once daily, dose to be adjusted according to response at
intervals of at least 1 week, maximum daily dose to be
given in 2–3 divided doses; maximum 2 g per day
▶Adult: Initially 500 mg once daily for at least 1 week,
dose to be taken with breakfast, then 500 mg twice
daily for at least 1 week, dose to be taken with breakfast
and evening meal, then 500 mg 3 times a day, dose to
be taken with breakfast, lunch and evening meal;
maximum 2 g per day
▶BY MOUTH USING MODIFIED-RELEASE MEDICINES
▶Adult: Initially 500 mg once daily, then increased if
necessary up to 2 g once daily, dose increased
gradually, every 10–15 days, dose to be taken with
evening meal, alternatively increased to 1 g twice daily,
dose to be taken with meals, alternative dose only to be
used if control not achieved with once daily dose
regimen. If control still not achieved then change to
standard release tablets
Type 2 diabetes mellitus [reduction in risk or delay of
onset]
▶BY MOUTH USING MODIFIED-RELEASE MEDICINES
▶Adult 18–74 years: Initially 500 mg once daily, then
increased if necessary up to 2 g once daily, dose
increased gradually, every 10–15 days, dose to be taken
with evening meal, for further information on risk
factors—consult product literature
Polycystic ovary syndrome
▶BY MOUTH USING IMMEDIATE-RELEASE MEDICINES
▶Adult: Initially 500 mg once daily for 1 week, dose to be
taken with breakfast, then 500 mg twice daily for
1 week, dose to be taken with breakfast and evening
meal, then 1.5–1.7 g daily in 2–3 divided doses
l UNLICENSED USE
▶In adults g Based on clinical experience of increased
side-effects, maximum dose for metformin immediate-
release medicines in BNF Publications differs from product
licence. l Not licensed for polycystic ovary syndrome.
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Risk factors for lactic acidosis
CAUTIONS, FURTHER INFORMATION
▶Risk factors for lactic acidosis Manufacturer advises caution
in chronic stable heart failure (monitor cardiac function),
and concomitant use of drugs that can acutely impair renal
function; interrupt treatment if dehydration occurs, and
avoid in conditions that can acutely worsen renal function,
or cause tissue hypoxia.
▶Elderly Prescription potentially inappropriate (STOPP
criteria) if eGFR less than 30 mL/minute/1.73 m2 (risk of
lactic acidosis). See also Prescribing in the elderly p. 33.
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GLUCOPHAGE ® SR
Scottish Medicines Consortium (SMC) decisions
The Scottish Medicines Consortium has advised (October
2009) that Glucophage ® SR is accepted for restricted use
within NHS Scotland for the treatment of type 2 diabetes
mellitus in adult patients who are intolerant of standard-
release metformin, and in whom the prolonged-release
tablet allows the use of a dose of metformin not previously
tolerated, or in patients for whom a once daily preparation
offers a clinically significant benefit.
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