Bendroflumethiazide
Indications
mild heart failure
familial hyperkalemia
edema
urinary tract disorders
Dosage
Administration/Absorption
Absorbed relatively rapidly after oral administration
Distribution
96% protein bound
Mechanism
Inhibits Na+/Cl- reabsorption at the beginning of the distal convoluted tubule (DCT) by blocking the thiazide-sensitive Na-Cl cotransporter
=> Excretion of sodium, chloride and water
This results in an increase in potassium excretion via the sodium-potassium exchange mechanism
Vasodilation
Mechanism unclear
Activating calcium-activated potassium channels (large conductance) in vascular smooth muscles?
Inhibiting various carbonic anhydrases in vascular tissue?
Thiazides also cause an increase in serum uric acid
Excretion
Half life 8.5 hrs
Side effects
Common adverse effects
impaired glucose tolerance
Rare adverse effects
Interactions
Contraindications