Midodrine (Intradialytic Hypotension)
Brand names: Bramox, Gutron
Midodrine is an oral alpha-adrenergic agonist used off-label to manage intradialytic hypotension in haemodialysis patients who drop their blood pressure during sessions, as well as for orthostatic hypotension.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
Its active metabolite desglymidodrine selectively stimulates peripheral alpha-1 adrenoceptors, causing arteriolar and venous vasoconstriction that raises peripheral vascular resistance and blood pressure.
Prescribing in practice
- Avoid late-day dosing and dosing near recumbency because midodrine can cause marked supine hypertension; for dialysis use it is typically taken shortly before the session rather than at bedtime.
- It is contraindicated in severe organic heart disease, acute kidney injury, urinary retention, phaeochromocytoma and thyrotoxicosis.
- Dose timing must be matched to the dialysis schedule, with the last dose well before lying down, and the indication remains unlicensed in the UK.
Monitoring
Monitor supine and standing (or pre- and post-dialysis) blood pressure and watch for supine hypertension, urinary symptoms and scalp paraesthesia.
Counselling the patient
- Take your dose before sitting upright for dialysis and avoid lying flat soon afterwards.
- Report headache, pounding in the chest when lying down, or difficulty passing urine.
Evidence & guidelines
Small trials and current prescribing references support its use for symptomatic and dialysis-associated hypotension, with the SPC reflecting its limited licensed scope.
Reference: Perez-Garcia et al. (Intradialytic Hypotension); KDOQI Haemodialysis Adequacy Guidelines; SPC Bramox/Gutron; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Hyperkalaemia Management · UK Kidney Association Guidelines 2020; NICE CKD Guidelines
- Rhabdomyolysis · Renal Association 2018; UpToDate 2024
- Hypocalcaemia (Adult) · Society for Endocrinology
- SIADH (Endocrine Perspective) · European Hyponatraemia Guidelines 2014
- Hepatorenal Syndrome · EASL 2018; ICA 2015
- Acute Kidney Injury (AKI) · KDIGO 2012 / NICE AKI 2019