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Pronunciation | /ˌkænəɡlɪˈfloʊzɪn/ KAN-ə-glif-LOH-zin |
Trade names | Invokana, Sulisent, Prominad, others |
Other names | JNJ-28431754; TA-7284; (1S)-1,5-anhydro-1-C-(3-{[5-(4-fluorophenyl)thiophen-2-yl]methyl]}-4-methylphenyl)-D-glucitol |
AHFS/Drugs.com | Monograph |
MedlinePlus | a613033 |
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Routes of administration | By mouth |
Drug class | SGLT2 inhibitor |
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Pharmacokinetic data | |
Bioavailability | 65% |
Protein binding | 99% |
Metabolism | Liver glucuronidation |
Elimination half-life | 11.8 (10–13) hours |
Excretion | 53% faecal and 33% kidney |
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ECHA InfoCard | 100.223.671 |
Chemical and physical data | |
Formula | C24H25FO5S |
Molar mass | 444.52 g·mol−1 |
3D model (JSmol) | |
Melting point | 98 °C (208 °F) |
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Canagliflozin, sold under the brand name Invokana among others, is a medication used to treat type 2 diabetes.[3] It is used together with exercise and diet.[3] It is not recommended in type 1 diabetes.[3] It is taken by mouth.[3]
Common side effects include vaginal yeast infections, nausea, constipation, and urinary tract infections.[3] Serious side effects may include low blood sugar, Fournier's gangrene, leg amputation, kidney problems, high blood potassium, and low blood pressure.[3] Diabetic ketoacidosis may occur despite nearly normal blood sugar levels.[3] Use in pregnancy and breastfeeding is not recommended.[1] Canagliflozin is a sodium-glucose cotransporter-2 (SGLT2) inhibitor.[3] It works by increasing the amount of glucose lost in the urine.[3]
Canagliflozin was approved for medical use in the United States, in the European Union, and in Australia in 2013.[3][4][5][6] It is on the World Health Organization's List of Essential Medicines.[7]
FDA approval
was invoked but never defined (see the help page).Invokana EPAR
was invoked but never defined (see the help page).