1. U.S. Food and Drug Administration (FDA). (2013). CARAFATE® (sucralfate) Tablets Prescribing Information. Section: WARNINGS. "In patients with chronic renal failure or those receiving dialysis
aluminum accumulation and toxicity (aluminum osteodystrophy
osteomalacia
encephalopathy) have been described." Available from the FDA website.
2. Brunton
L. L.
Dandan
R.
& Knollmann
B. C. (Eds.). (2017). Goodman & Gilman's The Pharmacological Basis of Therapeutics (13th ed.). McGraw-Hill Education. Chapter 49
Pharmacotherapy of Gastric Acidity
Peptic Ulcers
and Gastroesophageal Reflux Disease
Section: Mucosal Protective Agents. "Because a small amount of Al3+ is absorbed
sucralfate should be used with caution in patients with renal insufficiency
who are at risk for Al3+ overload."
3. DiPiro
J. T.
Yee
G. C.
Posey
L. M.
Haines
S. T.
Nolin
T. D.
& Ellingrod
V. (Eds.). (2020). Pharmacotherapy: A Pathophysiologic Approach (11th ed.). McGraw-Hill Education. Chapter 25
Peptic Ulcer Disease
Section: Mucosal Protective Agents. "Systemic absorption of aluminum is minimal but may be problematic in patients with chronic renal failure because of the risk of accumulation and toxicity."