Clinical data | |
---|---|
Trade names | Exelon, others |
AHFS/Drugs.com | Monograph |
MedlinePlus | a602009 |
License data |
|
Pregnancy category |
|
Routes of administration | By mouth, transdermal patch |
ATC code | |
Legal status | |
Legal status | |
Pharmacokinetic data | |
Bioavailability | 60 to 72% |
Protein binding | 40% |
Metabolism | Liver, via pseudocholinesterase |
Elimination half-life | 1.5 hours |
Excretion | 97% in urine |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
IUPHAR/BPS | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.120.679 |
Chemical and physical data | |
Formula | C14H22N2O2 |
Molar mass | 250.342 g·mol−1 |
3D model (JSmol) | |
| |
| |
(what is this?) (verify) |
Rivastigmine, sold under the brand name Exelon among others, is an acetylcholinesterase inhibitor used for the treatment of dementia associated with Alzheimer's disease and with Parkinson's disease.[4][6][7] Rivastigmine can be administered orally or via a transdermal patch; the latter form reduces the prevalence of side effects,[8] which typically include nausea and vomiting.[9]
Rivastigmine is eliminated through the urine, and appears to have relatively few drug-drug interactions.[9]
It was patented in 1985 and came into medical use in 1997.[10]
Winblad
was invoked but never defined (see the help page).Inglis
was invoked but never defined (see the help page).