Generic name: fosrenol
Availability: Prescription only
Pregnancy & Lactation: Risk data available
Brand names: Fosrenol, Lanthanum carbonate
Generic name: fosrenol
Availability: Prescription only
Pregnancy & Lactation: Risk data available
Brand names: Fosrenol, Lanthanum carbonate
Phosphate binder used to reduce the intestinal absorption of phosphates.
Reduction of serum phosphorus in patients with end-stage renal disease (ESRD). Reductions in serum phosphorus concentrations are similar to those achieved with alternative phosphate binders (e.g., calcium salts, sevelamer).
Risk of hypercalcemia apparently is less than with calcium (e.g., calcium carbonate) salts.
Administer orally in divided doses with or immediately after meals (in order to bind dietary phosphates efficiently).
Chew tablets completely before swallowing; do not swallow intact tablets.
Available as lanthanum carbonate; dosage expressed in terms of lanthanum.
Initially, 750 mg–1.5 g daily.
Adjust dosage at 2- to 3-week intervals until serum phosphorus concentration is acceptable; generally titrated in increments of 750 mg daily in clinical studies.
Dosage of 1.5–3 g daily usually is required to reduce serum phosphorus concentrations to <6 mg/dL; dosages up to 3.75 g daily have been studied.
Monitor serum phosphorus concentrations as needed during titration and regularly thereafter.
No known contraindications.
Safety and efficacy not established in active peptic ulcer disease, ulcerative colitis, Crohn’s disease, or bowel obstruction; use with caution in patients with these disorders.
Abdominal radiographs performed in patients taking lanthanum may have the typical radiopaque appearance of a radiograph performed using an imaging agent.
No differences in fracture or mortality rates were observed between patients receiving lanthanum and those receiving alternative therapy for up to 3 years in clinical studies; however, data are insufficient to conclude lanthanum has no effect on fracture or mortality rates beyond 3 years of use.
Category C.
Not known whether lanthanum is distributed into milk. Caution if used in nursing women.
Safety and efficacy not established in children <18 years of age.
Deposited in developing bone (including the growth plate) of animals in long-term studies; although growth abnormalities in animals were not observed, the consequences of deposition in developing bone of pediatric patients are unknown.
No substantial differences in safety and efficacy relative to younger adults.
Nausea, vomiting, dialysis graft occlusion, abdominal pain.
Administer orally in divided doses with or immediately after meals (in order to bind dietary phosphates efficiently).
Chew tablets completely before swallowing; do not swallow intact tablets.
Available as lanthanum carbonate; dosage expressed in terms of lanthanum.
Initially, 750 mg–1.5 g daily.
Adjust dosage at 2- to 3-week intervals until serum phosphorus concentration is acceptable; generally titrated in increments of 750 mg daily in clinical studies.
Dosage of 1.5–3 g daily usually is required to reduce serum phosphorus concentrations to <6 mg/dL; dosages up to 3.75 g daily have been studied.
Monitor serum phosphorus concentrations as needed during titration and regularly thereafter.
Not a substrate for CYP isoenzymes. Does not inhibit CYP isoenzymes 1A2, 2C9/10, 2C19, 2D6, or 3A4/5.
Pharmacokinetic interaction unlikely.
Possible formation of insoluble complexes; do not administer such drugs within 2 hours of lanthanum dose.
Drug |
Interaction |
---|---|
Citrate salts |
Lanthanum absorption not altered |
Digoxin |
No formation of insoluble complexes in vitro; digoxin absorption not altered |
Enalapril |
No formation of insoluble complexes in vitro |
Furosemide |
No formation of insoluble complexes in vitro |
Metoprolol |
No formation of insoluble complexes in vitro; metoprolol absorption not altered |
Phenytoin |
No formation of insoluble complexes in vitro |
Warfarin |
No formation of insoluble complexes in vitro; warfarin absorption not altered |