A study for a 32 year old man who takes Dexilant - from FDA reports


66 males aged 32 (±5) who take the same drug are studied. This is a personalized study for a 32 year old male patient who has Gerd. The study is created by eHealthMe based on reports from FDA.



On Apr, 15, 2018

66 males aged 32 (±5) who take Dexilant are studied.


Number of reports submitted per year:

Dexilant for a 32-year old man.

Information of the patient in this study:

  • Age: 32
  • Gender: male
  • Conditions: Gerd
  • Drugs taken:
    • Dexilant (dexlansoprazole)

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

  • Headaches: 0 (0% of males aged 32 (±5) who take the drug)

As an adverse outcome could be a symptom of a condition, additional studies are listed to help identify the cause: for example, regardless of which drug is taken, how many female HBP patients aged 50 (±5) have nausea

As an adverse outcome could be a side effect of a drug, additional studies are listed to help identify the cause: for example, how many female Aspirin users aged 50 (±5) have nausea

Most common side effects over time

< 1 month:
  • Nightmares (unpleasant dreams)
  • Proctalgia (pain in the rectum)
  • Hypersensitivity
  • Rashes (redness)
  • Clostridium difficile colitis (inflammation of colon by clostridium difficile bacteria infection)
  • Muscle spasms (muscle contraction)
  • Eye swelling
  • Itching
  • Abdominal pain
  • Diarrhea
1 - 6 months:
  • Dizziness
  • Ulcerative colitis (inflammatory bowel disease (ibd). it causes swelling, ulcerations, and loss of function of the large intestine)
  • Rashes (redness)
  • Pancreatitis (inflammation of pancreas)
  • Swelling face
  • Chest pain
  • Dry mouth
  • Itching
  • Disturbance in attention
  • Lymph node pain
6 - 12 months:
n/a
1 - 2 years:
n/a
2 - 5 years:
n/a
5 - 10 years:
n/a
10+ years:
n/a
not specified:
  • Abdominal pain
  • Rashes (redness)
  • Diarrhea
  • Colitis (inflammation of colon)
  • Crohn's disease (condition that causes inflammation of the gastrointestinal tract)
  • Panic disorder
  • Nausea (feeling of having an urge to vomit)
  • Stress and anxiety
  • Injection site pain
  • Fever

Top conditions involved for these people *:

  • Crohn's Disease (condition that causes inflammation of the gastrointestinal tract): 15 people, 22.73%
  • Indigestion : 9 people, 13.64%
  • Pain : 7 people, 10.61%
  • Ulcerative Colitis (inflammatory bowel disease (ibd). it causes swelling, ulcerations, and loss of function of the large intestine): 5 people, 7.58%
  • Psoriasis (immune-mediated disease that affects the skin): 5 people, 7.58%

Top co-used drugs for these people *:

  • Humira (18 people, 27.27%)
  • Prednisone (8 people, 12.12%)
  • Asacol (6 people, 9.09%)
  • Singulair (5 people, 7.58%)
  • Remicade (5 people, 7.58%)

* Some reports may have incomplete information.

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.

Want to find out more about the FDA reports used in the study? You can request them from FDA.

Related tests

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Expand this study to include FDA and eHealthMe reports

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What are the symtoms?

Could your drugs cause:

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NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also 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.