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Drug Interactions between biotin / chromium picolinate / cinnamon and pramlintide

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

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Interactions between your drugs

Moderate

chromium picolinate pramlintide

Applies to: biotin / chromium picolinate / cinnamon and pramlintide

MONITOR: Pharmacologic dosages of chromium (200 mcg/day or more for adults) may help improve diabetic control and reduce the requirements for insulin and other antidiabetic agents. Chromium appears to play a role in normal insulin function and glucose utilization, and some investigators have suggested that it increases insulin sensitivity and glucose tolerance and decreases blood glucose levels in certain diabetics, possibly those with low chromium levels. However, others have not corroborated these findings, and a few have even reported a negative effect on glucose tolerance and blood levels.

MANAGEMENT: Until further data are available, therapy with pharmacologic dosages of chromium should be administered cautiously in patients receiving insulin or other antidiabetic agents. Patients should be monitored for changes in diabetic medication requirements.

References (9)
  1. Bratman S, Kroll D. (2000) "The Natural Health Bible: From the Most Trusted Alternative Health Site in the World--Your A-Z Guide to over 300 Conditions, Herbs, Vitamins, and Supplements." Roseville, CA: Prima Health
  2. Mertz W (1998) "Interaction of chromium with insulin: a progress report." Nutr Rev, 56, p. 174-7
  3. Fox GN, Sabovic Z (1998) "Chromium picolinate supplementation for diabetes mellitus." J Fam Pract, 46, p. 83-6
  4. Anderson RA (1998) "Chromium, glucose intolerance and diabetes." J Am Coll Nutr, 17, p. 548-55
  5. Anderson RA, cheng N, Bryden NA, et al. (1997) "Elevated intakes of supplemental chromium improve glucose and insulin variables in individuals with type 2 diabetes." Diabetes, 46, p. 1786-91
  6. Abraham AS, Brooks BA, Eylath U (1992) "The effects of chromiium supplementation on serum glucose and lipids in patients with and without non-insulin-dependent diabetes." Metabolism, 41, p. 768-71
  7. Althuis MD, Jordan NE, Ludington EA, Wittes JT (2002) "Glucose and insulin responses to dietary chromium supplements: a meta-analysis." Am J Clin Nutr, 76, p. 148-55
  8. Gunton JE, Cheung NW, Hitchman R, et al. (2005) "Chromium supplementation does not improve glucose tolerance, insulin sensitivity, or lipid profile: a randomized, placebo-controlled, double-blind trial of supplementation in subjects with impaired glucose tolerance." Diabetes Care, 28, p. 712-3
  9. Martin J, Wang ZQ, Zhang XH, et al. (2006) "Chromium picolinate supplementation attenuates body weight gain and increases insulin sensitivity in subjects with type 2 diabetes." Diabetes Care, 29, p. 1826-32
Moderate

pramlintide cinnamon

Applies to: pramlintide and biotin / chromium picolinate / cinnamon

MONITOR: Coadministration of cinnamon with antidiabetic drugs and/or insulin may have additive blood glucose-lowering effects, which may potentiate the risk of hypoglycemia. Cinnamon has been shown in vitro to increase glucose uptake, glycogen synthesis and insulin sensitivity. However, clinical data are conflicting. Some small studies have reported that cinnamon reduced fasting blood glucose levels and/or glycosylated hemoglobin (HbA1c) in patients with type 2 diabetes, whereas others have not. In a randomized control trial (RCT) in people with type 2 diabetes (n=60), it was reported that, compared to placebo, daily doses of 1 g, 3 g, or 6 g of oral cinnamon (as Cinnamomum cassia) consumed for 40 days reduced fasting blood glucose levels by 18% to 29%. In addition, an unblinded RCT in patients with poorly controlled type 2 diabetes managed in primary care in the USA (n=109) reported that the addition of oral cinnamon 1 g daily (as C. cassia) for 90 days to usual care reduced HbA1c by a statistically significant 0.83% compared to usual care alone, which lowered HbA1c by 0.37%. However, in a double-blinded, RCT in people with type 2 diabetes (n=57), compared to placebo, the administration of oral cinnamon 1 g daily (as C. cassia) for three months did not demonstrate significant differences in fasting blood glucose or HbA1c from baseline to three months. Hypoglycemia was not reported as an adverse effect in these studies.

MANAGEMENT: Until more information is available, blood glucose should be monitored if antidiabetic agents are used concomitantly with cinnamon. 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 (3)
  1. Blevins SM, Leyva MJ, Brown J, Wright J, Scofield RH (2007) "Effect of cinnamon on glucose and lipid levels in non-insulin-dependent type 2 diabetes" Diabetes Care, 30, p. 2236-2237
  2. Khan A, Safdar M, Khan MMA, Khattak KN, Anderson RA (2003) "Cinnamon improves glucose and lipids of people with type 2 diabetes" Diabetes Care, 26, p. 3215-3218
  3. Crawford P (2009) "Effectiveness of cinnamon for lowering hemoglobin A1c in patients with type 2 diabetes: a randomised, controlled trial" J Am Board Fam Med, 22, p. 507-512

Drug and food interactions

Moderate

pramlintide food

Applies to: pramlintide

ADJUST DOSING INTERVAL: Pramlintide slows gastric emptying and may delay the absorption of concomitantly administered oral medications. In a pharmacokinetic study of 24 patients with type 2 diabetes, coadministration with pramlintide (120 mcg) decreased the peak plasma concentration (Cmax) of acetaminophen (1000 mg) by 29% and increased its time to peak plasma concentration (Tmax) based on the time of acetaminophen administration relative to pramlintide injection. Pramlintide significantly increased acetaminophen Tmax (range 48 to 72 minutes) when acetaminophen was administered simultaneously with or up to 2 hours following pramlintide injection, but it had negligible effect when acetaminophen was administered 1 to 2 hours before pramlintide injection.

MANAGEMENT: When rapid onset of a concomitantly administered oral medication is critical to its effectiveness, the medication should be administered at least 1 hour before or 2 hours after pramlintide injection.

References (1)
  1. (2005) "Product Information. Symlin (pramlintide)." Amphastar 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.