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Drug Interactions between pentamidine and semaglutide

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Moderate

pentamidine semaglutide

Applies to: pentamidine and semaglutide

MONITOR: Pentamidine may interfere with the therapeutic effects of insulin and other antidiabetic agents. The use of pentamidine has been associated with disturbances in blood glucose homeostasis due to direct toxic effects on beta cells of the pancreas. Hypoglycemia, which may be severe and/or prolonged, as well as hyperglycemia and insulin-dependent diabetes mellitus, the latter of which may be irreversible, have been reported. The onset of pentamidine-induced hypoglycemia generally varied from 5 to 7 days after start of therapy to several days after therapy stops. In some cases, hyperglycemia and progression to diabetes followed, although these effects have occurred independently also. Pancreatic toxicity has been reported with both parenteral use and, less frequently, oral inhalation of pentamidine. The risk appears to be related to total cumulative dosage and prior therapy with the drug, particularly within the last 3 months. Renal impairment also appears to be a risk factor.

MANAGEMENT: Blood glucose should be monitored closely during and after pentamidine therapy in patients receiving insulin or other antidiabetic agents, especially if they are elderly or have renal impairment. Patients should learn to recognize the symptoms of hypoglycemia such as headache, dizziness, drowsiness, nervousness, confusion, tremor, hunger, weakness, perspiration, palpitation, and tachycardia. If hypo- or hyperglycemia occur during pentamidine therapy, patients should initiate appropriate remedial therapy immediately and contact their physician. Dosage adjustments may be required if an interaction is suspected.

References (16)
  1. Bouchard PH, Sai P, Reach G, et al. (1982) "Diabetes mellitus following pentamidine-induced hypoglycemia in humans." Diabetes, 31, p. 40-5
  2. Stahl-Bayliss CM, Kalman CM, Laskin OL (1986) "Pentamidine-induced hypoglycemia in patients with the acquired immune deficiency syndrome." Clin Pharmacol Ther, 39, p. 271-5
  3. Shen M, Orwoll ES, Conte JE, Prince MJ (1989) "Pentamidine-induced pancreatic beta-cell dysfunction." Am J Med, 86, p. 726-8
  4. Millard PS, van der Horst C (1991) "Reversible diabetes mellitus after intravenous pentamidine." Am J Med, 91, p. 442
  5. Wood G, Wetzig N, Hogan P, Whitby M (1991) "Survival from pentamidine induced pancreatitis and diabetes mellitus." Aust N Z J Med, 21, p. 341-2
  6. "Product Information. Nebupent (pentamidine)." Fujisawa
  7. (2001) "Product Information. Pentam 300 (pentamidine)." Fujisawa
  8. Kallas EG, Galvao LL, Roland RK, Medeiros EA, Levi GC, Mendonca JS (1993) "Pentamidine induced ketoacidosis in acquired immunodeficiency syndrome patients." Int Conf AIDS, 9, p. 474
  9. Ostrowski M, Walmsley S, Pluemecke G, Salit I, Rachlis A, Krajden S (1993) "Pentamidine-induced diabetes mellitus (PIDM)." Int Conf AIDS, 9, p. 465
  10. Liegl U, Bogner JR, Goebel FD (1994) "Insulin-dependent diabetes mellitus following pentamidine therapy in a patient with AIDS." Clin Investig, 72, p. 1027-9
  11. Assan R, Mayaud C, Perronne C, Matheron S, Assan D, Zucman D, Chotard L (1995) "Pentamidine-induced derangements of glucose homeostasis: determinant roles of renal failure and drug accumulation - a study of 128 patients." Diabetes Care, 18, p. 47-55
  12. Coyle P, Carr AD, Depczynski BB, Chisholm DJ (1996) "Diabetes mellitus associated with pentamidine use in HIV-infected patients." Med J Aust, 165, p. 587-8
  13. Chan JC, Cockram CS, Critchley JA (1996) "Drug-induced disorders of glucose metabolism. Mechanisms and management." Drug Saf, 15, p. 135-57
  14. (2001) "Product Information. Lantus (insulin glargine)." Aventis Pharmaceuticals
  15. (2022) "Product Information. NovoLOG (insulin aspart)." Novo Nordisk Pharmaceuticals Inc
  16. Hardy H, Esch LD, Morse GD (2001) "Glucose disorders associated with HIV and its drug therapy." Ann Pharmacother, 35, p. 343-51

Drug and food interactions

Moderate

semaglutide food

Applies to: semaglutide

ADJUST DOSING INTERVAL: Taking oral semaglutide with food, beverage, or other oral medications may alter semaglutide absorption and exposure. In a controlled study with healthy volunteers, limited or no measurable semaglutide exposure was observed in subjects that were fed 30 minutes prior to taking oral semaglutide, while all subjects that fasted overnight and 30 minutes after the oral semaglutide dose had measurable semaglutide exposure. Area under the curve (AUC) and semaglutide peak plasma concentration (Cmax) were approximately 40% greater in subjects that fasted compared to those who did not. AUC and Cmax were also increased with a post-dose fasting period greater than 30 minutes.

MANAGEMENT: It is recommended that oral semaglutide be taken 30 minutes before the first food, beverage, or other oral medications of the day with no more than 4 ounces of plain water to ensure its efficacy. Fasting longer than 30 minutes after the oral semaglutide dose may lead to increased gastrointestinal side effects including nausea, vomiting, or diarrhea.

References (4)
  1. (2024) "Product Information. Rybelsus (semaglutide)." Novo Nordisk Pharmaceuticals Inc
  2. (2024) "Product Information. Rybelsus (semaglutide)." Novo Nordisk Canada Inc
  3. (2024) "Product Information. Rybelsus (semaglutide)." Novo Nordisk Ltd
  4. Baekdal TA, Breitschaft A, Donsmark M, Maarbjerg SJ, Sondergaard FL, Borregaard J (2021) "Effect of various dosing conditions on the pharmacokinetics of oral semaglutide, a human glucagon-like peptide-1 analogue in a tablet formulation" Diabetes Ther, 12, p. 1915-27

Therapeutic duplication warnings

No warnings were found for your selected drugs.

Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.