Alpha₁-Adrenergic Agonist (Vasopressor — Oral)
Pregnancy: Contraindicated — vasoconstriction may cause placental ischaemia.
Midodrine
Brand names: Bramox, ProAmatine
Adult dose
Dose: Hepatorenal syndrome type 1 (with albumin, when terlipressin not available): 7.5mg three times daily (titrate to 12.5mg TDS if needed). Orthostatic hypotension: 2.5–10mg three times daily (morning, midday, late afternoon — last dose at least 4 hours before bedtime).
Route: Oral
Frequency: Three times daily
Max: 40mg/day
For hepatorenal syndrome (HRS-1): used in combination with octreotide (200 micrograms SC TDS) and albumin (20–40g/day IV) as an alternative when terlipressin unavailable. For orthostatic hypotension: take final dose ≥4 hours before bedtime — supine hypertension risk when lying down.
Paediatric dose
Route: N/A
Frequency: N/A
Max: Seek specialist opinion
Not licensed in children. Limited evidence. Seek specialist opinion.
Dose adjustments
Renal
Use with caution in renal impairment — increased risk of supine hypertension and urinary retention. Avoid if eGFR <30.
Hepatic
Primary use is in hepatic disease. No specific dose reduction; titrate carefully.
Clinical pearls
- HRS treatment combination: midodrine 7.5–12.5mg TDS + octreotide 200 micrograms SC TDS + albumin 20–40g/day IV — used when terlipressin is unavailable or contraindicated.
- Terlipressin is superior to midodrine/octreotide for HRS-1 reversal — use terlipressin first-line when available (CONFIRM trial: terlipressin + albumin achieved HRS reversal in 32% vs 17% with placebo).
- Supine hypertension: a key safety concern — patients must take the last dose at least 4 hours before lying down. Monitor lying and standing BP.
- Orthostatic hypotension: effective for autonomic failure and dialysis-associated hypotension — different from HRS use.
Contraindications
- Severe organic heart disease
- Urinary retention
- Phaeochromocytoma
- Thyrotoxicosis
- Supine hypertension (systolic >180mmHg)
- Acute renal failure not caused by circulatory dysfunction
Side effects
- Supine hypertension (most important — do not take within 4 hours of bedtime)
- Paraesthesia (scalp tingling — common alpha₁ agonist effect)
- Urinary retention (especially in men with BPH)
- Pilomotor reactions (goosebumps)
- Nausea, headache
Interactions
- Cardiac glycosides (digoxin): additive bradycardia risk (reflex bradycardia from hypertension)
- Alpha-blockers (doxazosin, tamsulosin): antagonise vasopressor effect
- Fludrocortisone: additive pressor effect — monitor blood pressure closely
- MAOIs: severe hypertensive crisis — contraindicated combination
Monitoring
- Blood pressure (lying and standing — supine hypertension and postural effect)
- Renal function (creatinine — monitor HRS reversal)
- Urinary output
- Heart rate
Reference: BNFc; BNF 90; EASL Cirrhosis Guidelines 2018; CONFIRM Trial (Wong et al, NEJM 2021); SPC Bramox. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
Pathways
- Lower Gastrointestinal Bleed · BSG 2019; NICE NG141
- Variceal Upper GI Bleed · BSG 2015; Baveno VII (2022)
- Spontaneous Bacterial Peritonitis (SBP) · BSG / EASL 2018
- Hepatorenal Syndrome · EASL 2018; ICA 2015
- Hepatic Encephalopathy · EASL 2014; West Haven criteria
- Clostridioides difficile Colitis · NICE NG199 (2021); IDSA/SHEA 2021