A study for a 51 year old woman who takes Jardiance - from FDA reports

214 females aged 51 (±5) who take the same drug are studied. This is a personalized study for a 51 year old female patient who has Weight Management. The study is created by eHealthMe based on reports from FDA.

On Jun, 18, 2018

214 females aged 51 (±5) who take Jardiance are studied.

Number of reports submitted per year:

Jardiance for a 51-year old woman.

Information of the patient in this study:

  • Age: 51
  • Gender: female
  • Conditions: Weight Management
  • Drugs taken:
    • Jardiance (empagliflozin)

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

  • Swelling Of The Face: 0 (0% of females aged 51 (±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:
  1. Diabetic ketoacidosis (diabetic ketoacidosis (dka) is high concentrations of ketone bodies)
  2. Dizziness
  3. Sepsis (a severe blood infection that can lead to organ failure and death)
  4. Vision blurred
  5. Nausea (feeling of having an urge to vomit)
1 - 6 months:
  1. Glycosylated haemoglobin increased
  2. Cholecystitis acute (rapid infection of gallbladder)
  3. Hepatomegaly (abnormal enlargement of the liver)
  4. Liver function test abnormal
  5. Mouth ulcers
6 - 12 months:
  1. Kidney stones
  2. Pancreatitis acute (sudden inflammation of pancreas)
  3. Hypovolaemia (a decreased volume of circulating blood in the body)
  4. Blood urea increased
  5. Altered state of consciousness (altered state of mind)
1 - 2 years:
  1. Blood glucose increased
  2. Dizziness
  3. Diabetic ketoacidosis (diabetic ketoacidosis (dka) is high concentrations of ketone bodies)
  4. Glomerular filtration rate decreased
  5. Headache (pain in head)
2 - 5 years:
  1. Hypoglycemia (low blood sugar)
  2. Hepatic cirrhosis (chronic liver disease characterized by replacement of liver tissue by fibrosis, scar tissue)
5 - 10 years:
10+ years:
not specified:
  1. Diabetic ketoacidosis (diabetic ketoacidosis (dka) is high concentrations of ketone bodies)
  2. Fungal infection
  3. Blood glucose increased
  4. Diarrhea
  5. Weight decreased

Top conditions involved for these people *:

  1. Type 2 Diabetes : 107 people, 50.00%
  2. Diabetes : 53 people, 24.77%
  3. High Blood Pressure : 29 people, 13.55%
  4. High Blood Cholesterol : 13 people, 6.07%
  5. Type 1 Diabetes : 9 people, 4.21%

Top co-used drugs for these people *:

  1. Metformin (52 people, 24.30%)
  2. Lantus (15 people, 7.01%)
  3. Victoza (13 people, 6.07%)
  4. Insulin (9 people, 4.21%)
  5. Trulicity (9 people, 4.21%)

* 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.

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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.