Who have Breast cancer female with Sumatriptan - from FDA reports

Breast cancer female is found among people who take Sumatriptan, especially for people who are 50-59 old also take medication Provera, and have Hormone replacement therapy. This study is created by eHealthMe based on reports of 7,412 people who have side effects when taking Sumatriptan from FDA, and is updated regularly.

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On Feb, 10, 2019

7,412 people reported to have side effects when taking Sumatriptan.
Among them, 10 people (0.13%) have Breast cancer female

Number of reports submitted per year:

Could Sumatriptan cause Breast cancer female?

Age of people who have Breast cancer female when taking Sumatriptan *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 0.0 %
  • 40-49: 11.11 %
  • 50-59: 66.67 %
  • 60+: 22.22 %

Top conditions involved for these people *:

  1. Hormone Replacement Therapy: 9 people, 90.00%
  2. Crohn's Disease (condition that causes inflammation of the gastrointestinal tract): 1 person, 10.00%

Top co-used drugs for these people *:

  1. Provera: 9 people, 90.00%
  2. Premarin: 8 people, 80.00%
  3. Cafergot: 3 people, 30.00%
  4. Prempro: 3 people, 30.00%
  5. Estrace: 2 people, 20.00%
  6. Topamax: 2 people, 20.00%
  7. Synthroid: 2 people, 20.00%
  8. Drospirenone And Ethinyl Estradiol: 2 people, 20.00%
  9. Diazepam: 1 person, 10.00%
  10. Folic Acid: 1 person, 10.00%

* Approximation only. Some reports may have incomplete information.

Do you have Breast cancer female while taking Sumatriptan?

You are not alone:

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Sumatriptan side effects

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FDA reports used in this study

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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.

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