canagliflozin

General

Pronunciation:
kan-a-gli-floe-zin


Trade Name(s)

  • Invokana

Ther. Class.
antidiabetics

Pharm. Class.
sodium-glucose co-transporter 2 (SGLT2) inhibitors

Indications

  • Adjunct to diet and exercise in the management of type 2 diabetes mellitus.
  • May be used with other antidiabetic agents.

Action

Inhibits proximal renal tubular sodium-glucose co-transporter 2 (SGLT2), which determines reabsorption of glucose from the tubular lumen. Inhibits reabsorption of glucose, lowers renal threshold for glucose, and increases excretion of glucose in urine.

Therapeutic Effect(s):

Improved glycemic control.

Pharmacokinetics

Absorption: Well absorbed (65%) following oral administration.

Distribution: Extensive tissue distribution.

Protein Binding: 99%

Metabolism and Excretion: Mostly metabolized by UDP-glucuronyl transferases (UGT) to inactive metabolites, minimal metabolism by CYP3A4 (7%). 50% excreted in feces as parent drug and metabolites, 33% as metabolites in urine, <1% excreted in urine as unchanged drug.

Half-life: 10.6 hr

TIME/ACTION PROFILE (effects on A1C)

ROUTEONSETPEAKDURATION
POunknownunknown24 hr

Contraindication/Precautions

Contraindicated in:

  • Hypersensitivity;
  • Severe renal impairment (eGFR <45 mL/min/1.73 m2 ), end-stage renal disease or on dialysis;
  • Type 1 diabetes;
  • Severe hepatic impairment;
  • Lactation:Avoid use, discontinue breast feeding or discontinue canagliflozin.

Use Cautiously in:

  • eGFR <60 mL/min/1.73 m2 (monitor frequently) (↑ risk of adverse reactions related to ↓ intravascular volume);
  • History of pancreatitis, pancreatic surgery, reduced caloric intake due to illness or surgery, or alcohol abuse (↑ risk of ketoacidosis);
  • Hypovolemia, chronic kidney disease, HF, or concurrent use of diuretics, NSAIDs, ACE inhibitors, or ARBs (↑ risk of acute kidney injury);
  • Previous amputation, peripheral vascular disease, or neuropathy (↑ risk of limb amputation);
  • Geri: ↑ risk of adverse reactions related to ↓ intravascular volume;
  • Hypotension (correct prior to treatment, especially if eGFR 30–60 mL/min, age >75 yr, or concurrent use of loop diuretics, ACE inhibitors, or ARBs;
  • OB: Use during pregnancy only if potential maternal benefit justifies potential fetal risk;
  • Pedi: Safety and effectiveness not established.

Adverse Reactions/Side Effects

CV: hypotension

GI: abdominal pain, constipation, nausea

GU: UROSEPSIS, female mycotic infections, acute kidney injury, glucosuria, male mycotic infections, ↓ renal function, urinary tract infection (including pyelonephritis), ↑ urination, vulvovaginal pruritus

Endo: hypoglycemia (↑ with other medications)

F and E: KETOACIDOSIS, hyperkalemia, hypermagnesemia, hyperphosphatemia, thirst

Metabolic: hyperlipidemia

MS: bone fractures

Misc: HYPERSENSITIVITY REACTIONS (INCLUDING ANAPHYLAXIS OR ANGIOEDEMA)

* CAPITALS indicate life-threatening.
Underline indicate most frequent.

Interactions

Drug-Drug

  • Blood levels are ↓ by UGT inducers including phenobarbital, phenytoin, rifampin, and ritonavir; ↑dose may be required.
  • ↑ risk of hypoglycemia with insulin or insulin secretagogues; dose adjustments may be required.
  • May ↑ blood levels and effects of digoxin; levels should be monitored.
  • ↑ risk of hyperkalemia with potassium-sparing diuretics or medications that interfere with the renin-angiotensin-aldosterone system.
  • Concurrent use with NSAIDs, diuretics, ACE inhibitors, or angiotensin receptor blockers may ↑ risk of acute kidney injury.

Route/Dosage

PO: (Adults) eGFR ≥ 60 mL/min/1.73 m2 100 mg once daily initially, may be ↑ to 300 mg once daily; Concurrent use of UGT inducers (phenobarbital, phenytoin, rifampin, ritonavir)– if maintenance dose is 100 mg daily, may require ↑ to 300 mg daily.

Renal Impairment
PO: (Adults) eGFR 45–60 mL/min/1.73 m2 100 mg once daily.

Availability

Tablets: 100 mg, 300 mg

In Combination with:metformin (Invokamet); metformin XR (Invokamet XR). See combination drugs.

Assessment

  • Observe patient for signs and symptoms of hypoglycemic reactions (abdominal pain, sweating, hunger, weakness, dizziness, headache, tremor, tachycardia, anxiety).
  • Monitor for signs and symptoms of volume depletion (dizziness, feeling faint, weakness, orthostatic hypotension) after initiating therapy.
  • Monitor for infection, new pain, tenderness, sores, or ulcers involving lower limbs; discontinue canagliflozin if these occur.

Lab Test Considerations: Monitor hemoglobin A1C prior to and periodically during therapy.

  • May cause ↑ uric acid levels.
  • May ↑ serum creatinine and ↓ eGFR. Monitor renal function, especially in patients with eGFR <60 mL/min/1.73 m2 .
  • May cause ↑ serum potassium, magnesium, and phosphate levels. Monitor electrolytes periodically during therapy.
  • May cause ↑ LDL-C. Monitor serum lipid levels periodically during therapy.
  • Causes positive test for urine glucose.

Potential Diagnoses

Implementation

  • Patients stabilized on a diabetic regimen who are exposed to stress, fever, trauma, infection, or surgery may require administration of insulin.
  • Correct volume depletion prior to beginning therapy with canagliflozin.
  • PO: Administer before the first meal of the day.

Patient/Family Teaching

  • Instruct patient to take canagliflozin as directed. Take missed doses as soon as remembered, unless it is almost time for next dose; do not double doses. Advise patient to read the Medication Guide before starting and with each Rx refill in case of changes.
  • Explain to patient that canagliflozin helps control hyperglycemia but does not cure diabetes. Therapy is usually long term.
  • Instruct patient not to share this medication with others, even if they have the same symptoms; it may harm them.
  • Encourage patient to follow prescribed diet, medication, and exercise regimen to prevent hyperglycemic or hypoglycemic episodes.
  • Review signs of hypoglycemia and hyperglycemia with patient. If hypoglycemia occurs, advise patient to take a glass of orange juice or 2–3 tsp of sugar, honey, or corn syrup dissolved in water, and notify health care professional.
  • Instruct patient in proper testing of blood glucose and urine ketones. Inform patient that canagliflozin will cause a positive test result when testing for urine glucose. Monitored closely during periods of stress or illness and health care professional notified if significant changes occur.
  • Inform patient that canagliflozin may cause yeast infections. Women may have signs and symptoms of a vaginal yeast infection (vaginal odor, white or yellow vaginal discharge [may be lumpy or look like cottage cheese], vaginal itching). Men may have signs and symptoms of a yeast infection of the penis (redness, itching, or swelling of penis; rash on penis; foul smelling discharge from penis; pain in skin around penis). Advise patient to notify health care professional if yeast infection occurs.
  • Advise patient to notify health care professional promptly if rash; hives; or swelling of face, lips, or throat occur.
  • Inform patient of increased risk for urinary tract infections, hypotension, and bone fractures and discuss factors that may increase risk.
  • Advise patient to notify health care professional of all Rx or OTC medications, vitamins, or herbal products being taken and to consult with health care professional before taking other medications, especially other oral hypoglycemic medications.
  • Advise patient to notify health care professional if pregnancy is planned or suspected or if breast feeding.

Evaluation/Desired Outcomes

Improved hemoglobin A1C and glycemic control in adults with Type II diabetes.

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TY - ELEC T1 - canagliflozin ID - 110121 A1 - Quiring,Courtney, AU - Sanoski,Cynthia A, AU - Vallerand,April Hazard, BT - Davis's Drug Guide UR - https://anesth.unboundmedicine.com/anesthesia/view/Davis-Drug-Guide/110121/all/canagliflozin PB - F.A. Davis Company ET - 16 DB - Anesthesia Central DP - Unbound Medicine ER -