Sodium-Glucose Co Transporter 2 (SGLT2) Inhibitors and Cycloset Flashcards
Sodium-Glucose Co Transporter 2 (SGLT2) Inhibitors, Dapagliflozin (Farxiga) and Canaglifolozin (Invokana) MOA:
Inhibits SGLT2 in proximal renal tubules
=increases urinary glucose excretion, lowering plasma glucose levels
What is SGLT2 responsible for?
Reabsorption of filtered glucose from the kidneys
When can SGLT2 inhibitors be administered?
With or without food (won’t cause hypoglycemia by itself)
Peak effect and half life of SGLT2 inhibitors:
Peak: 1-2hrs
Half-life: 12hrs
SGLT2 inhibitors should only be used in patients with CrCL >_____
60mL/min
Laboratory changes that may happen with SGLT2 inhibitors include:
Increases in Scr and decreases in eGFR
Increases in LDL
What should be corrected in patients prior to administration and why?
Volume depletion
Drugs causes volume contraction, putting patients at risk for hypotension
AE of SGLT2 inhibitors include:
Female genital fungal infections
UTI
Hypoglycemia when used with combo therapy
Bladder cancer (unknown causal association
Cycloset (bromocriptine) is used to treat which type of DM?
Type 2
What is Cycloset’s MOA:
Dopamine agonist
Exact mechanism of glycemic control unknown
Improves glycemic control without increasing insulin concentrations
Cycloset AE:
GI upset: N/C
CNS effects: dizziness, HA, fatigue
Impulsive/compulsive behavior (when used to treat Parkinson’s)
How is Cycloset metabolized?
CYP3A4. Also inhibits 3A4.
Drug interactions