Dicyclomine hydrochloride and Ulcerative colitis - from FDA reports

Ulcerative colitis is found among people who take Dicyclomine hydrochloride, especially for people who are female, 40-49 old also take medication Lotronex, and have Pain. This study is created by eHealthMe based on reports of 550 people who have side effects when taking Dicyclomine hydrochloride from FDA, and is updated regularly.

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On Oct, 15, 2018

550 people reported to have side effects when taking Dicyclomine hydrochloride.
Among them, 11 people (2.0%) have Ulcerative colitis

Number of reports submitted per year:

Could Dicyclomine hydrochloride cause Ulcerative colitis?

Gender of people who have Ulcerative colitis when taking Dicyclomine hydrochloride *:

  • female: 90.91 %
  • male: 9.09 %

Age of people who have Ulcerative colitis when taking Dicyclomine hydrochloride *:

Top conditions involved for these people *:

  1. Pain: 2 people, 18.18%
  2. Sleep Disorder: 1 person, 9.09%
  3. Colitis (inflammation of colon): 1 person, 9.09%
  4. Birth Control: 1 person, 9.09%

Top co-used drugs for these people *:

  1. Lotronex: 6 people, 54.55%
  2. Zelnorm: 3 people, 27.27%
  3. Ibuprofen: 2 people, 18.18%
  4. Xyrem: 1 person, 9.09%
  5. Uceris: 1 person, 9.09%

Click here to view more results or personalize the results to your gender and age

Top other side effects for these people *:

  1. Weight Decreased: 5 people, 45.45%
  2. Abdominal Tenderness: 4 people, 36.36%
  3. Nausea (feeling of having an urge to vomit): 4 people, 36.36%
  4. Colitis Ischaemic (due to infection of intestine impaired blood supply to colon): 4 people, 36.36%
  5. White Blood Cell Count Increased: 3 people, 27.27%

Click here to view more results or personalize the results to your gender and age

* Approximation only. Some reports may have incomplete information.

FDA reports used in this study

Do you have Ulcerative colitis while taking Dicyclomine hydrochloride?

You are not alone:

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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.

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

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