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New search Medicine profile Metformin / Glibenclamide

Clinical medicine profile

Metformin / Glibenclamide

Biguanide antidiabetic

POM
Evidence state Source not available Reviewed 14 Aug 2026
Route
ORAL
Schedule
POM
ATC
Not assigned
PPB status
registered
Patient advice Check interactions
Verification required

This profile needs source confirmation

A traceable source link is not attached to this profile. Confirm prescribing decisions against the current SmPC and Kenya STG/EML.

01 Risk first

Safety essentials

The information most likely to change a prescribing or dispensing decision.

Contraindications

  • Severe renal impairment (thresholds per label, often eGFR <30).
  • Acute conditions predisposing to hypoxia/acidosis (shock, severe HF, severe infection).
  • Acute alcohol intoxication.
  • Hypersensitivity.

Precautions

  • Hold around iodinated contrast if eGFR low (local protocol).
  • B12 deficiency with long-term use — monitor if anaemic/neuropathy.
  • GI titration improves tolerability.
  • XR formulations reduce GI effects.
02 Point of care

Dosing matrix

Population and organ-function guidance, shown together for faster comparison.

Adult

Initial dose: One tablet (5mg /500mg) OD (Max. daily dose: 20mg/2000mg)

Paediatric

See label paediatric section if present; otherwise use paediatric formulary — do not extrapolate adult doses.

Renal

Dose by eGFR; stop if severe impairment or acute kidney injury.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.
Hepatic

Avoid in significant hepatic impairment (lactic acidosis risk).

03 Clinical use

Use, effects & interactions

Indications

  • Uncomplicated and non-ketonic diabetes mellitus (maturity onset type II diabetes).
  • Clinical selection for Metformin / Glibenclamide should follow culture results where relevant, Kenya STG/EML recommendations, and the current product SmPC.
  • Class context: Biguanide antidiabetic.
  • Confirm site-specific dose, duration and monitoring before prescribing.

Adverse effects

  • [Metformin] Diarrhoea, nausea, abdominal discomfort, metallic taste.
  • Serious: lactic acidosis (rare, high mortality if occurs). [Glibenclamide] GI disturbances
  • blood dyscrasia
  • hypoglycaemia
  • jaundice
  • skin rashes
  • hypersensitivity reactions
  • headache
  • dizziness
  • hyponatraemia
  • paraesthesia
  • photosensitivity.
  • Fixed-dose/multi-ingredient product.
  • Clinical details partially inherited from component monographs: Metformin, Glibenclamide.
  • Confirm combination SmPC for exact dosing.
04 Pharmacology

Mechanism & disposition

See under glibenclamide and metformin respectively Metformin decreases hepatic gluconeogenesis, improves peripheral insulin sensitivity, and reduces intestinal glucose absorption.

See under glibenclamide and metformin resp…Does not stimulate insulin secretion — low…
Read complete mechanism

See under glibenclamide and metformin respectively Metformin decreases hepatic gluconeogenesis, improves peripheral insulin sensitivity, and reduces intestinal glucose absorption. Does not stimulate insulin secretion — low intrinsic hypoglycaemia risk alone.

Onset

Days for glycaemic effect

Duration

Taken daily chronically

Route

ORAL

Absorption

saturable. Not metabolised; renally excreted unchanged. Accumulation in renal impairment drives lactic acidosis risk. [Glibenclamide] Absorption,

Elimination

are product-specific. Consider food effects, protein binding, hepatic CYP/UGT

Half-life

when adjusting for organ impairment, age and drug interactions. Verify parameters in the current SmPC.

05 Special populations

Pregnancy, lactation & diet

Pregnancy

[Metformin] Increasingly used in GDM/PCOS pathways per specialist protocols; insulin remains standard in many settings. [Glibenclamide] Use only if potential benefit justifies potential risk; prefer agents with better reproductive data when alternatives exist.

Lactation

Generally considered compatible.

06 Kenya market

Brands & loaded prices

From
Median
Listings0
BrandManufacturerPackObserved price
No reviewed brand listings are linked yet.
07 Provenance

Sources & review state

Primary sourceLocal active-ingredient clinical extract; Component monographs (multi-source pipeline); Professional class pharmacology (Biguanide antidiabetic)
Last reviewed14 Aug 2026
EvidenceSource not available

Decision support only. Confirm patient-specific decisions against the current product SmPC, Kenya STG/EML, and professional judgement.