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| PubChem = 3085017 | PubChem = 3085017
| DrugBank = APRD01226 | DrugBank = APRD01226
| ChEMBL = 1201798
| KEGG = D08512 | KEGG = D08512
| chemical_formula = <sub>m</sub><br />where a+b:c = 9:1 | chemical_formula = <sub>m</sub><br />where a+b:c = 9:1

Revision as of 15:57, 10 February 2011

Pharmaceutical compound
Sevelamer
Clinical data
Pregnancy
category
Routes of
administration
oral
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailabilitynil
Metabolismnil
Elimination half-lifen/a
Excretionfaecal 100%
Identifiers
IUPAC name
  • poly(allylamine-
    co-N,N'-diallyl-1,3-diamino-2-hydroxypropane)
CAS Number
PubChem CID
DrugBank
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
Formulam
where a+b:c = 9:1
Molar massvariable

Sevelamer (rINN) (Template:Pron-en, Template:IPA-en) is a phosphate binding drug used to prevent hyperphosphatemia in patients with chronic renal failure. When taken with meals, sevelamer binds to dietary phosphate and prevents its absorption. It is marketed by Genzyme under the trade names Renagel and Renvela (carbonate formulation).

Chemistry and pharmacology

Sevelamer is a copolymer of 2-(chloromethyl)oxirane (epichlorohydrin) and prop-2-en-1-amine. The marketed form sevelamer hydrochloride is a partial hydrochloride salt being present as approximately 40% amine hydrochloride and 60% sevelamer base. The amine groups of sevelamer become partially protonated in the intestine and interact with phosphorus molecules through ionic and hydrogen bonding.

Clinical use

Indications

Sevelamer is indicated for the management of hyperphosphataemia in adult patients with stage 4 and 5 chronic renal failure on hemodialysis.

Contraindications

Sevelamer therapy is contraindicated in hypophosphataemia or bowel obstruction.

Adverse effects

Common adverse drug reactions (ADRs) associated with the use of sevelamer include: hypotension, hypertension, nausea and vomiting, dyspepsia, diarrhea, flatulence, and/or constipation.

Other effects

Sevelamer can significantly reduce serum uric acid. This reduction has no known detrimental effect and several beneficial effects, including reducing hyperuricemia, uric acid nephrolithiasis, and gout.

External links

References

  1. Garg JP, Chasan-Taber S, Blair A; et al. (2005). "Effects of sevelamer and calcium-based phosphate binders on uric acid concentrations in patients undergoing hemodialysis: a randomized clinical trial". Arthritis and rheumatism. 52 (1): 290–5. doi:10.1002/art.20781. PMID 15641045. {{cite journal}}: Explicit use of et al. in: |author= (help); Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
Drugs for treatment of hyperkalemia and hyperphosphatemia (V03AE)
Potassium binders
Phosphate binders
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