Phosphate Binder (Lanthanum-Based)
Lanthanum Carbonate 750mg–3g/day (Fosrenol)
Brand names: Fosrenol
Adult dose
Dose: 750mg per meal initially (2250mg/day); titrate in increments of 750mg every 2–3 weeks based on serum phosphate. Usual maintenance: 1500–3000mg/day in divided doses.
Route: Oral (chewable tablet — must be chewed, not swallowed whole)
Frequency: Three times daily with or immediately after meals
Max: 3750mg/day
Titrate to target serum phosphate <1.78 mmol/L (dialysis patients). Chewable tablets — partial chewing then swallowing is acceptable. Available as 500mg, 750mg, 1000mg chewable tablets. Powder for oral suspension also available.
Paediatric dose
Route: N/A
Frequency: N/A
Max: Not licensed in children — insufficient safety data
Not licensed for use in patients <18 years.
Dose adjustments
Renal
No dose adjustment required — not systemically absorbed; designed specifically for dialysis/CKD patients
Hepatic
No dose adjustment required — not hepatically metabolised
Clinical pearls
- Non-calcium, non-aluminium phosphate binder — avoids hypercalcaemia (unlike calcium carbonate/acetate) and aluminium toxicity (unlike aluminium hydroxide)
- Must be chewed with or immediately after meals — binding dietary phosphate in upper GI tract is the mechanism; swallowing whole significantly reduces efficacy
- Lanthanum has low systemic absorption (<0.001%) — bone accumulation reported in long-term animal studies but not confirmed clinically significant in humans over 10+ years of use
- KDIGO CKD-MBD 2017: choice of phosphate binder should be individualised — lanthanum carbonate is preferred over calcium-based binders when hypercalcaemia is present
- Patient counselling essential — chewable tablets are unpalatable; compliance is a common issue; powder formulation available as alternative
Contraindications
- Hypophosphataemia
- Bowel obstruction or ileus
- Hypersensitivity to lanthanum carbonate
Side effects
- Nausea and vomiting (especially initial titration period)
- Diarrhoea
- Constipation
- Abdominal pain
- Headache
- GI obstruction (rare — chew thoroughly)
Interactions
- Fluoroquinolones (ciprofloxacin, levofloxacin) — lanthanum reduces absorption; take 2h before lanthanum
- Levothyroxine — reduced absorption; take 2h apart
- Other drugs bound in GI tract — separate administration by 2h where clinically important
Monitoring
- Serum phosphate (every 1–3 months)
- Serum calcium (to ensure no hypocalcaemia)
- GI symptoms (nausea, bowel habit)
Reference: BNFc; BNF; KDIGO CKD-MBD Guidelines 2017; Fosrenol SPC; NICE TA117. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
- HE-MACS (History and ECG-Based Manchester ACS Risk Score) · ACS Risk Stratification
- Weight-Based Levothyroxine Dose Calculator · Thyroid
- Number Needed to Treat (NNT) / Number Needed to Harm (NNH) · Evidence-Based Medicine
- HIV Opportunistic Infection Risk (CD4-Based) · HIV / Immunodeficiency
- Calcium-Phosphate Product · Electrolytes
- Estimated Bladder Capacity (Age-based) · Urodynamics
Pathways
- 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