6
Medications
Verify before prescribing: All drug names and doses below are Murtagh's printed reference figures — cross-check against current eTG/local formulary, renal function (eGFR) and the individual's cardiovascular/renal risk profile before prescribing. Diabetes pharmacotherapy is a fast-moving area (SGLT2/GLP-1 positioning in particular) — treat this list as a starting structure, not current best practice.
Staged approach
- 1. Lifestyle (diet + exercise) trial for 3-6 months first in type 2 diabetes
- 2. If HbA1c target not met: start metformin (first-line) — usual starting dose 500mg once or twice daily
- 3. If target not met after further 3-6 months: add a second agent — SGLT2 inhibitor or GLP-1 receptor agonist are now preferred second-line (particularly with cardiovascular disease, heart failure, multiple CV risk factors or kidney disease); DPP-4 inhibitors are an option where CV/renal risk is low or SGLT2/GLP-1 not tolerated; sulfonylureas and glitazones are valid but now largely superseded given they lack proven CV/renal benefit
- 4. Insulin may be required at any stage, particularly if symptomatic hyperglycaemia or HbA1c remains well above target — for less experienced GPs, shared care with an endocrinologist is recommended
- Review the need for continued oral therapy after 3 months of treatment; avoid prescribing an oral hypoglycaemic agent prematurely without a genuine lifestyle trial first
First-line agents
Biguanide — metformin
Verify dose
Examples: Metformin 500mg once or twice daily, titrated; duration of action ~12h (slow-release once-daily formulation available); usual range 0.5-3g/day
Favoured in: First-line for essentially all type 2 diabetes — good tolerance, low cost, no significant weight gain, no hypoglycaemia, improved lipid profile
Avoid / caution: Avoid in significant cardiac, hepatic or kidney disease (eGFR <30)
Key side effects: GI disturbance (diarrhoea, nausea/vomiting) — common; lactic acidosis — rare but serious, risk low if therapeutic dose not exceeded and renal function adequate
Second-line agents
SGLT2 inhibitor ('gliflozin')
Verify dose
Examples: Empagliflozin 10-25mg daily; Dapagliflozin 5-10mg daily; Ertugliflozin 5-15mg daily
Favoured in: Preferred second-line, particularly with CVD, heart failure, multiple CV risk factors or kidney disease — proven cardiovascular/renal protective benefits; also causes meaningful weight loss
Avoid / caution: Withhold during acute illness, fasting, or peri-surgery (risk of euglycaemic DKA)
Key side effects: Genitourinary infections, dehydration, dizziness, hypoglycaemia (when combined with insulin/sulfonylurea); diabetic ketoacidosis risk if withheld incorrectly during illness/fasting
GLP-1 receptor agonist
Verify dose
Examples: Dulaglutide 1.5mg weekly (SC); Exenatide 5mcg bd or 2mg weekly MR (SC); Liraglutide 0.6-1.8mg daily (SC)
Favoured in: Preferred second-line alongside SGLT2 inhibitors; greatest HbA1c reduction of any non-insulin agent when added to metformin (0.6-1.5%); proven CV benefit in high-risk patients; substantial sustained weight loss (2-6kg over 12 months)
Key side effects: Nausea (common), pancreatitis (rare)
DPP-4 inhibitor ('gliptin')
Verify dose
Examples: Sitagliptin 25-100mg daily; Linagliptin 5mg daily; Vildagliptin 50-100mg daily; Alogliptin 25mg daily
Favoured in: Where cardiovascular/renal risk is low, or an SGLT2 inhibitor/GLP-1 agonist is contraindicated or not tolerated
Key side effects: Slight pancreatitis risk; rhinorrhoea, headache, hypersensitivity (e.g. urticaria); dizziness/fatigue (vildagliptin)
Sulfonylurea
Verify dose
Examples: Gliclazide 40-320mg daily; Glipizide 2.5-40mg daily; Glibenclamide 2.5-20mg daily; Glimepiride 1-4mg daily
Favoured in: Valid option but increasingly superseded by SGLT2i/GLP-1 agonists, which have proven CV/renal benefit that sulfonylureas lack
Avoid / caution: Caution in elderly — prefer a shorter-acting agent (e.g. gliclazide); longer-acting potent agents cause troublesome hypoglycaemia in the elderly
Key side effects: Hypoglycaemia (most common), weight gain (common), rash and GI effects (rare)
Alpha-glucosidase inhibitor
Verify dose
Examples: Acarbose 150-600mg daily
Favoured in: Adjunct option
Key side effects: Flatulence, skin rashes, diarrhoea, liver effects
Thiazolidinedione ('glitazone')
Verify dose
Examples: Pioglitazone 15-45mg daily; Rosiglitazone 4-8mg daily
Favoured in: Dubious mortality benefit — largely superseded
Avoid / caution: Heart failure (caution)
Key side effects: Oedema, weight gain, heart failure; hepatic effects and fracture risk (rosiglitazone)
Insulin
Verify dose
Examples: Ultra-short (lispro/aspart/glulisine, e.g. Humalog/NovoRapid/Apidra); short-acting neutral (Actrapid/Humulin R); intermediate isophane/NPH (Protaphane/Humulin NPH); long-acting analogues (glargine/detemir, e.g. Lantus/Levemir); pre-mixed combinations (e.g. Humalog Mix 25/50, NovoMix 30)
Favoured in: Any stage if HbA1c remains above target on oral therapy, or symptomatic hyperglycaemia; shared care with endocrinology recommended for less experienced GPs; continuous subcutaneous insulin infusion (pump) uses rapid-acting insulin
Key side effects: Hypoglycaemia — teach recognition and treatment; injection site issues
7
Acute / severe presentations
Four metabolic emergencies to recognise promptly in a person with diabetes.
Hypoglycaemia (BGL <4.0 mmol/L, serious <3.0)
Most common with insulin (any type) and sulfonylureas (metformin rarely causes it). Warning symptoms: sweating, tremor, palpitations, hunger, peri-oral paraesthesia — may progress rapidly to loss of consciousness without warning ('hypoglycaemic unawareness' after recurrent episodes). If alert and able to swallow: 15g refined carbohydrate orally (e.g. 7 jelly beans, 3 tsp sugar/honey, half glass juice/soft drink); recheck BGL every 15 min, repeat if still <4; once >4 give a complex carbohydrate snack. If reduced conscious state/unconscious: 30mL 50% glucose slow IV push (or rectally via syringe nozzle if no IV access, 10mL in children) OR 1mL (1 ampoule) glucagon IM/SC (0.5mL if child <25kg); call an ambulance if unconscious. Follow up with snack/meal once conscious; admit if concerned; identify the cause.
Diabetic ketoacidosis (DKA)
Life-threatening; develops over days (hours in 'brittle' diabetes), usually when insulin is omitted during illness (opposite advice applies to SGLT2 inhibitors — withhold these when unwell or fasting, including peri-surgery or during deliberate low-calorie intake, to avoid precipitating DKA). Features: hyperglycaemia (often >20 mmol/L, can be lower/normal if on an SGLT2 inhibitor), polyuria/polydipsia/drowsiness, vomiting and abdominal pain, dehydration, hyperventilation (acidotic breathing) with low BP and high pulse/resp rate, ketosis. Management: urgent hospital admission; early IV fluids (normal saline fast first litre, then caution); IV insulin (e.g. 10U in first hour); sodium, potassium (KCl) and fluid replacement; ECG for arrhythmia from electrolyte disturbance.
Hyperosmolar hyperglycaemic state (HHS)
Altered conscious state (stupor to coma) with marked dehydration, typically insidious onset over weeks with fatigue/polyuria/polydipsia, in uncontrolled type 2 diabetes (especially elderly) without significant ketosis. Often an underlying precipitant (e.g. pneumonia, UTI). Mortality is even higher than DKA. Treatment: IV fluids (normal to half-normal saline, given slowly) and insulin at relatively lower doses than for DKA.
Lactic acidosis
Marked hyperventilation ('air hunger') and confusion, high mortality; consider in the very ill patient taking metformin, especially with impaired kidney function. Investigations show low pH, low bicarbonate, high lactate, absent serum ketones, large anion gap. Treatment: remove the cause, rehydration, IV sodium bicarbonate.
This page summarises structure and content from Murtagh's General Practice for personal point-of-care use. Medication names and doses are the book's printed reference figures and are explicitly flagged to verify — check current eTG/local formulary guidance and the individual patient's renal function, comorbidities and interactions before prescribing.