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Drug Interactions between exenatide and ginseng

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

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Interactions between your drugs

Moderate

ginseng exenatide

Applies to: ginseng and exenatide

MONITOR: Coadministration of ginseng with antidiabetic drugs may potentiate the risk of hypoglycemia. Clinical data are conflicting. Some small studies have reported that ginseng reduced the blood levels of glucose and/or glycosylated hemoglobin (HbA1c) in diabetic patients, whereas others have not. Furthermore, the lack of standardized preparations of ginseng may limit the generalization of study results. In a double-blind, randomized cross-over trial, 24 diabetic patients received either 1 g/meal (3 g/day) of American ginseng (AG) extract or placebo for 8 weeks while maintaining their original antidiabetic treatments. Compared to placebo, AG significantly reduced HbA1c by 0.29% and fasting blood glucose by 0.71 mmol/L. In another study, 36 non-insulin dependent diabetic patients received 100 mg or 200 mg ginseng extract containing 4 mg or 8 mg of ginsenoside, respectively or placebo once daily for 8 weeks. Compared to placebo, HbA1c was reduced by 0.5% and fasting blood glucose by 0.9 mmol/L in the 200 mg ginseng extract group. However, in contrast, other randomized, double-blind, placebo controlled studies reported no effect of ginseng on HbA1c.

MANAGEMENT: Until more information is available, blood glucose should be monitored if antidiabetic agents are used concomitantly with ginseng. Patients should be advised on the potential signs and symptoms of hypoglycemia (e.g., headache, dizziness, drowsiness, nervousness, confusion, tremor, hunger, weakness, perspiration, palpitation, and tachycardia), how to treat it, and to contact their doctor if it occurs. Patients should also be advised to take precautions to avoid hypoglycemia while driving or operating hazardous machinery.

References (7)
  1. Vuksan V, Sievenpiper JL, Koo VY, et al. (2000) "American ginseng (Panax quinquefolius L) reduces postprandial glycemia in nondiabetic subjects and subjects with type 2 diabetes mellitus." Arch Intern Med, 160, p. 1009-13
  2. Carabin IG, Burdock GA, Chatzidakis C (2000) "Safety assessment of panax ginseng." Int J Toxicol, 19, p. 293-301
  3. Vuksan V, Sung MK, Sievenpiper JL, et al. (2008) "Korean red ginseng (Panax ginseng) improves glucose and insulin regulation in well-controlled, type 2 diabetes: results of a randomized, double-blind, placebo-controlled study of efficacy and safety." Nutr Metab Cardiovasc Dis, 18, p. 46-56
  4. Vuksan V, Sievenpiper JL, Koo VY, et al. (2000) "Efficacy and safety of Panax ginseng berry extract on glycemic control: A 12-wk randomized, double-blind, and placebo controlled trial." Arch Intern Med, 160, p. 1009-13
  5. Vuskan V, Xu ZZ, Jovanovski E, et al. (2019) "Efficacy and safety of American ginseng (Panax quinquefolius L) extract on glycemic control and cardiovascular risk factors in individuals with type 2 diabetes: a double-blind, randomized, cross-over clinical trial." Eur J Nutr, 58, p. 1237-45
  6. Sotaniemi EA, Haapakoski E, Rautio A (1995) "Ginseng therapy in non-insulin-dependent diabetic patients." Diabetes Care, 18, p. 1373-5
  7. Win HH, Anderson R (2019) "Hypoglycemia due to "conception-enhancing" oral supplement." Endocr Pract, 24, p. 88-9

Drug and food interactions

Moderate

exenatide food

Applies to: exenatide

ADJUST DOSING INTERVAL: Exenatide slows gastric emptying and may reduce the extent and rate of absorption of concomitantly administered oral medications. When acetaminophen 1000 mg was administered simultaneously with exenatide 10 mcg and also one hour, 2 hours, and 4 hours after exenatide injection, acetaminophen systemic exposure (AUC) was decreased by 21%, 23%, 24%, and 14%, respectively; peak plasma concentration (Cmax) was decreased by 37%, 56%, 54%, and 41%, respectively; and time to peak plasma concentration (Tmax) was increased from 0.6 hours in the control period to 0.9 hours, 4.2 hours, 3.3 hours, and 1.6 hours, respectively. These values were not significantly changed when acetaminophen was given one hour before exenatide injection.

MANAGEMENT: Concomitantly administered oral medications that are dependent on threshold concentrations for efficacy (e.g., antibiotics, contraceptives) or that require rapid gastrointestinal absorption (e.g., hypnotics, pain medications) should be administered at least 1 hour before exenatide. If such medications are to be administered with food, patients should be advised to take them with a meal or snack when exenatide is not administered.

References (1)
  1. (2005) "Product Information. Byetta (exenatide)." Amylin Pharmaceuticals Inc

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.