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With BYETTA®, there is no increased risk of hypoglycemia when used with metformin and/or a TZD


Safety and tolerability:
Details about hypoglycemia and nausea


Hypoglycemia


  No increased risk of hypoglycemia in combination with metformin and/or a TZD.

  Sulfonylureas increase the risk of hypoglycemia.[2] When BYETTA is used with a sulfonylurea, there is an increased risk of hypoglycemia. To reduce this risk, reduction in the dose of the sulfonylurea may be considered.



Nausea


  The most common adverse event in the 30-week clinical trials was nausea (44% vs 18% for placebo).

  Almost all of these events were characterized as mild to moderate (94% vs 95% for placebo), and decreased over time in most patients.[1]

  In a study vs insulin glargine, the rates were similar to the 30-week trials.[1]

  3% dropout rate due to nausea over 30 weeks in clinical trials (vs <1% for placebo).

  Most patients who experienced nausea experienced it upon initiation of therapy.





BYETTA is indicated as adjunctive therapy to improve glycemic control in patients with type 2 diabetes mellitus who are taking metformin, a sulfonylurea, a thiazolidinedione, a combination of metformin and a sulfonylurea, or a combination of metformin and a thiazolidinedione, but have not achieved adequate glycemic control.

For Important Safety Information, please click here and for complete safety profile and other important prescribing considerations, see the full Prescribing Information.

References