Review: could Byetta cause Diabetic Gastroparesis?


Summary

Diabetic gastroparesis is found among people who take Byetta, especially for people who are female, 40-49 old , have been taking the drug for 1 - 2 years, also take medication Prilosec, and have Dyspepsia . We study 48,521 people who have side effects while taking Byetta from FDA and social media. Among them, 12 have Diabetic gastroparesis. Find out below who they are, when they have Diabetic gastroparesis and more.

You are not alone

Join a support group for people who take Byetta and have Diabetic gastroparesis >>>

Personalized health information

On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>

Byetta

Byetta has active ingredients of exenatide synthetic. It is often used in type 2 diabetes. (latest outcomes from Byetta 48,688 users)

Diabetic Gastroparesis

Diabetic gastroparesis (paralysis of the muscles of the stomach caused by diabetes) has been reported by people with electrocardiogram qt prolonged, breathing difficulty, extrapyramidal disorder, stress and anxiety, tardive dyskinesia (latest reports from 580 Diabetic gastroparesis patients).

On Jul, 22, 2016

48,521 people reported to have side effects when taking Byetta.
Among them, 12 people (0.02%) have Diabetic Gastroparesis


Number of reports submitted per year:

Could Byetta cause Diabetic gastroparesis?

Time on Byetta when people have Diabetic Gastroparesis *:

  • < 1 month: 28.57 %
  • 1 - 6 months: 0.0 %
  • 6 - 12 months: 14.29 %
  • 1 - 2 years: 42.86 %
  • 2 - 5 years: 14.29 %
  • 5 - 10 years: 0.0 %
  • 10+ years: 0.0 %

Gender of people who have Diabetic Gastroparesis when taking Byetta *:

  • female: 58.33 %
  • male: 41.67 %

Age of people who have Diabetic Gastroparesis when taking Byetta *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 20 %
  • 40-49: 40 %
  • 50-59: 10 %
  • 60+: 30 %

Severity if Diabetic Gastroparesis when taking Byetta **:

  • least: 0.0 %
  • moderate: 100 %
  • severe: 0.0 %
  • most severe: 0.0 %

How people recovered from Diabetic Gastroparesis **:

  • while on drug: 0.0 %
  • after off the drug: 0.0 %
  • not yet: 100 %

Top conditions involved for these people *:

  • Dyspepsia (3 people)
  • Type 2 Diabetes Mellitus (2 people)
  • Nausea (2 people)
  • Depression (2 people)
  • Major Depression (1 person)

Top co-used drugs for these people *:

  • Prilosec (5 people)
  • Synthroid (4 people)
  • Risperdal (4 people)
  • Lipitor (4 people)
  • Actos (4 people)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

Do you have Diabetic gastroparesis when taking Byetta?

Browse all side effects of Byetta

a b c d e f g h i j k l m n o p q r s t u v w x y z

Drugs that are associated with Diabetic gastroparesis

Diabetic gastroparesis

Could your condition cause Diabetic gastroparesis

Diabetic gastroparesis

You may be interested in these reviews

More reviews for: Byetta, Diabetic gastroparesis


NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.