| Systematic (IUPAC) name | |
|---|---|
| poly(allylamine- co-N,N'-diallyl-1,3-diamino-2-hydroxypropane) |
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| Clinical data | |
| Trade names | Renagel |
| AHFS/Drugs.com | monograph |
| MedlinePlus | a601248 |
| Pregnancy cat. | B3 (Australia), C (US) |
| Legal status | Schedule 4 (Australia), Rx only (US) |
| Routes | oral |
| Pharmacokinetic data | |
| Bioavailability | nil |
| Metabolism | nil |
| Half-life | n/a |
| Excretion | faecal 100% |
| Identifiers | |
| CAS number | 52757-95-6 |
| ATC code | V03AE02 |
| PubChem | CID 3085017 |
| DrugBank | APRD01226 |
| ChemSpider | 2341997 |
| UNII | 941N5DUU5C |
| KEGG | D08512 |
| ChEMBL | CHEMBL1201798 |
| Chemical data | |
| Formula | [(C3H7N)a+b.(C9H17N2O)c]m where a+b:c = 9:1 |
| Mol. mass | variable |
| (what is this?) (verify) |
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Sevelamer (rINN) ( /sɛˈvɛləmər/ or /sɛˈvɛləmɪər/) is a phosphate binding drug used to prevent hyperphosphatemia in patients with chronic renal failure. When taken with meals, it binds to dietary phosphate and prevents its absorption. It is marketed by Genzyme under the trade names Renagel (sevelamer hydrochloride) and Renvela (sevelamer carbonate).
Contents |
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.
Sevelamer is indicated for the management of hyperphosphataemia in adult patients with stage 4 and 5 chronic renal failure on hemodialysis.
Sevelamer therapy is contraindicated in hypophosphataemia or bowel obstruction.
Common adverse drug reactions (ADRs) associated with the use of sevelamer include: hypotension, hypertension, nausea and vomiting, dyspepsia, diarrhea, flatulence, and/or constipation.
Sevelamer can significantly reduce serum uric acid.[1] This reduction has no known detrimental effect and several beneficial effects, including reducing hyperuricemia, uric acid nephrolithiasis, and gout.
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