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. Author manuscript; available in PMC: 2016 Nov 1.
Published in final edited form as: Semin Dial. 2015 Aug 17;28(6):610–619. doi: 10.1111/sdi.12412

Table 1.

Comparison of the Currently Available Phosphate Binders

Binder Advantages Disadvantages Forms Dosage (mg)
Calcium Carbonate
  • Effective

  • Inexpensive

  • Readily available (over the counter)

  • Long-term experience

  • Potential hypercalcemia

  • Potential for progression of vascular calcification

  • GI side effects

  • Low-turnover bone disease

  • Tablet, chewable

  • Capsule

  • Liquid

  • Gum

  • Contains 40% elemental calcium (200mg elemental calcium per 500mg)

Calcium Acetate
  • Effective

  • Inexpensive

  • Readily available

  • Long-term experience

  • Potentially less calcium absorption than calcium carbonate

  • Potential hypercalcemia

  • Potential for progression of vascular calcification

  • GI side effects

  • Low-turnover bone disease

  • Tablet

  • Capsule

  • Liquid

  • Contains 25% elemental calcium (160mg elemental calcium per 667 mg capsule)

  • Total dose of elemental calcium should not exceed 2,000–2,500 mg/day

Magnesium Carbonate/Calcium Acetate
  • Effective

  • Inexpensive

  • Decreased calcium load compared with calcium-based binders

  • Potential hypermagnesemia

  • Potential hypercalcemia

  • GI side effects

  • No long-term experience

  • Tablet

  • 235 mg/435 mg

  • Maximum dose is 3–6 pills/day

Aluminum hydroxide
  • Very effective

  • Inexpensive

  • Potential for aluminum toxicity

  • GI side effects

  • Altered bone mineralization

  • Anemia

  • Tablet

  • Capsule

  • Liquid

  • 300–600 mg 3 times per day

  • Aluminum content varies from 100 to >200 mg per tablet

  • Limit use to no more than 4 weeks

Lanthanum Carbonate
  • Effective

  • Calcium free

  • Expensive

  • Potential for lanthanum accumulation in bone and tissue

  • GI side effects

  • No long-term data

  • Tablet, Chewable

  • Powder

  • 500–1,000 mg (3–6 chewable tablets) 3 times per day

Sevelamer hydrochloride
  • Effective

  • Calcium free

  • Pleiotropic effects

  • Expensive

  • GI side effects

  • Metabolic acidosis

  • Potential interferes with vitamin D and vitamin K absorption

  • Potentially decreased vascular calcification

  • Tablet

  • 800–1600 mg 3 times per day

  • Maximum dose studied 13 grams/day

Sevelamer Carbonate
  • Effective

  • Calcium free

  • Pleiotropic effects

  • No metabolic acidosis

  • Expensive

  • GI side effects

  • Potential interferes with vitamin D and vitamin K absorption

  • Potentially decreased vascular calcification

  • Tablet

  • Powder

  • 800–1600 mg 3 times per day

  • Maximum dose studied 14 grams/day

Sucroferric Oxyhydroxide
  • Effective

  • Calcium free

  • Less pill burden than sevelamer

  • Potential to raise transferrin, iron and hemoglobin levels

  • Expensive

  • GI side effects

  • Cannot be prescribed with oral levothyroxine or paricalcitol

  • Long-term side effects unknown

  • Unknown if iron accumulation long-term

  • Tablets, chewable

  • 500 mg (1 tablet) 3 times per day

  • Maximum dose is 3,000 mg/day

Ferric Citrate
  • Effective

  • Calcium free

  • Less pill burden than sevelamer

  • Potential to raise transferrin, iron and hemoglobin levels

  • Potential to decrease iron and ESA usage

  • Expensive

  • GI side effects

  • Long-term side effects unknown

  • Unknown if iron accumulation long-term

  • Tablets

  • Each tablet contains 210 mg ferric iron

  • Starting dose: 2 tablets 3 times per day

  • Maximum dose is 12 tablets per day

Mg= milligrams; GI= gastrointestinal; ESA= erythropoietin stimulation agents