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Drug Interactions between cinnamon and Humulin 70/30

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

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Interactions between your drugs

Moderate

insulin regular cinnamon

Applies to: Humulin 70 / 30 (insulin isophane / insulin regular) and 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

  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

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Moderate

insulin isophane (NPH) cinnamon

Applies to: Humulin 70 / 30 (insulin isophane / insulin regular) and 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

  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

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Drug and food interactions

Moderate

insulin regular food

Applies to: Humulin 70 / 30 (insulin isophane / insulin regular)

GENERALLY AVOID: Alcohol may cause hypoglycemia or hyperglycemia in patients with diabetes. Hypoglycemia most frequently occurs during acute consumption of alcohol. Even modest amounts can lower blood sugar significantly, especially when the alcohol is ingested on an empty stomach or following exercise. The mechanism involves inhibition of both gluconeogenesis as well as the counter-regulatory response to hypoglycemia. Episodes of hypoglycemia may last for 8 to 12 hours after ethanol ingestion. By contrast, chronic alcohol abuse can cause impaired glucose tolerance and hyperglycemia. Moderate alcohol consumption generally does not affect blood glucose levels in patients with well controlled diabetes. A disulfiram-like reaction (e.g., flushing, headache, and nausea) to alcohol has been reported frequently with the use of chlorpropamide and very rarely with other sulfonylureas.

MANAGEMENT: Patients with diabetes should avoid consuming alcohol if their blood glucose is not well controlled, or if they have hypertriglyceridemia, neuropathy, or pancreatitis. Patients with well controlled diabetes should limit their alcohol intake to one drink daily for women and two drinks daily for men (1 drink = 5 oz wine, 12 oz beer, or 1.5 oz distilled spirits) in conjunction with their normal meal plan. Alcohol should not be consumed on an empty stomach or following exercise.

References

  1. Jerntorp P, Almer LO (1981) "Chlorpropamide-alcohol flushing in relation to macroangiopathy and peripheral neuropathy in non-insulin dependent diabetes." Acta Med Scand, 656, p. 33-6
  2. Jerntorp P, Almer LO, Holin H, et al. (1983) "Plasma chlorpropamide: a critical factor in chlorpropamide-alcohol flush." Eur J Clin Pharmacol, 24, p. 237-42
  3. Barnett AH, Spiliopoulos AJ, Pyke DA, et al. (1983) "Metabolic studies in chlorpropamide-alcohol flush positive and negative type 2 (non-insulin dependent) diabetic patients with and without retinopathy." Diabetologia, 24, p. 213-5
  4. Hartling SG, Faber OK, Wegmann ML, Wahlin-Boll E, Melander A (1987) "Interaction of ethanol and glipizide in humans." Diabetes Care, 10, p. 683-6
  5. (2002) "Product Information. Diabinese (chlorpropamide)." Pfizer U.S. Pharmaceuticals
  6. (2002) "Product Information. Glucotrol (glipizide)." Pfizer U.S. Pharmaceuticals
  7. "Product Information. Diabeta (glyburide)." Hoechst Marion-Roussel Inc, Kansas City, MO.
  8. Skillman TG, Feldman JM (1981) "The pharmacology of sulfonylureas." Am J Med, 70, p. 361-72
  9. (2002) "Position Statement: evidence-based nutrition principles and recommendations for the treatment and prevention of diabetes related complications. American Diabetes Association." Diabetes Care, 25(Suppl 1), S50-S60
  10. Cerner Multum, Inc. "UK Summary of Product Characteristics."
View all 10 references

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Moderate

insulin isophane (NPH) food

Applies to: Humulin 70 / 30 (insulin isophane / insulin regular)

GENERALLY AVOID: Alcohol may cause hypoglycemia or hyperglycemia in patients with diabetes. Hypoglycemia most frequently occurs during acute consumption of alcohol. Even modest amounts can lower blood sugar significantly, especially when the alcohol is ingested on an empty stomach or following exercise. The mechanism involves inhibition of both gluconeogenesis as well as the counter-regulatory response to hypoglycemia. Episodes of hypoglycemia may last for 8 to 12 hours after ethanol ingestion. By contrast, chronic alcohol abuse can cause impaired glucose tolerance and hyperglycemia. Moderate alcohol consumption generally does not affect blood glucose levels in patients with well controlled diabetes. A disulfiram-like reaction (e.g., flushing, headache, and nausea) to alcohol has been reported frequently with the use of chlorpropamide and very rarely with other sulfonylureas.

MANAGEMENT: Patients with diabetes should avoid consuming alcohol if their blood glucose is not well controlled, or if they have hypertriglyceridemia, neuropathy, or pancreatitis. Patients with well controlled diabetes should limit their alcohol intake to one drink daily for women and two drinks daily for men (1 drink = 5 oz wine, 12 oz beer, or 1.5 oz distilled spirits) in conjunction with their normal meal plan. Alcohol should not be consumed on an empty stomach or following exercise.

References

  1. Jerntorp P, Almer LO (1981) "Chlorpropamide-alcohol flushing in relation to macroangiopathy and peripheral neuropathy in non-insulin dependent diabetes." Acta Med Scand, 656, p. 33-6
  2. Jerntorp P, Almer LO, Holin H, et al. (1983) "Plasma chlorpropamide: a critical factor in chlorpropamide-alcohol flush." Eur J Clin Pharmacol, 24, p. 237-42
  3. Barnett AH, Spiliopoulos AJ, Pyke DA, et al. (1983) "Metabolic studies in chlorpropamide-alcohol flush positive and negative type 2 (non-insulin dependent) diabetic patients with and without retinopathy." Diabetologia, 24, p. 213-5
  4. Hartling SG, Faber OK, Wegmann ML, Wahlin-Boll E, Melander A (1987) "Interaction of ethanol and glipizide in humans." Diabetes Care, 10, p. 683-6
  5. (2002) "Product Information. Diabinese (chlorpropamide)." Pfizer U.S. Pharmaceuticals
  6. (2002) "Product Information. Glucotrol (glipizide)." Pfizer U.S. Pharmaceuticals
  7. "Product Information. Diabeta (glyburide)." Hoechst Marion-Roussel Inc, Kansas City, MO.
  8. Skillman TG, Feldman JM (1981) "The pharmacology of sulfonylureas." Am J Med, 70, p. 361-72
  9. (2002) "Position Statement: evidence-based nutrition principles and recommendations for the treatment and prevention of diabetes related complications. American Diabetes Association." Diabetes Care, 25(Suppl 1), S50-S60
  10. Cerner Multum, Inc. "UK Summary of Product Characteristics."
View all 10 references

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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.