A study for a 76 year old woman who takes Furosemide - from FDA reports


39,091 females aged 76 (±5) who take the same drug are studied. This is a personalized study for a 76 year old female patient who has Diabetes. The study is created by eHealthMe based on reports from FDA.

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On Dec, 05, 2018

39,091 females aged 76 (±5) who take Furosemide are studied.


Number of reports submitted per year:

Furosemide for a 76-year old woman.

Information of the patient in this study:

  • Age: 76
  • Gender: female
  • Conditions: Diabetes
  • Drugs taken:
    • Furosemide (furosemide)

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

  • Skin Rash: 689 (1.76% of females aged 76 (±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. Pneumonia
  2. Acute kidney failure
  3. Agranulocytosis (a deficiency of granulocytes in the blood, causing increased vulnerability to infection)
  4. Renal failure acute (rapid kidney dysfunction)
  5. Anaemia (lack of blood)
1 - 6 months:
  1. Hypokalemia (low potassium)
  2. Urinary tract infection
  3. Renal failure acute (rapid kidney dysfunction)
  4. Cardiac failure
  5. Hyperkalemia (damage to or disease of the kidney)
6 - 12 months:
  1. Renal failure acute (rapid kidney dysfunction)
  2. Urinary tract infection
  3. Atrial fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles)
  4. Sepsis (a severe blood infection that can lead to organ failure and death)
  5. Thrombocytopenia (decrease of platelets in blood)
1 - 2 years:
  1. Dehydration (dryness resulting from the removal of water)
  2. Renal failure acute (rapid kidney dysfunction)
  3. Hypotension (abnormally low blood pressure)
  4. Hyperkalemia (damage to or disease of the kidney)
  5. Fainting (loss of consciousness and postural tone)
2 - 5 years:
  1. Anaemia (lack of blood)
  2. Nausea and vomiting
  3. Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
  4. Breathing difficulty
  5. Fever
5 - 10 years:
  1. Renal failure acute (rapid kidney dysfunction)
  2. Sepsis (a severe blood infection that can lead to organ failure and death)
  3. Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
  4. Infection
  5. Hyperkalemia (damage to or disease of the kidney)
10+ years:
  1. Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
  2. Hypokalemia (low potassium)
  3. Haemorrhage (bleeding)
  4. Cardiac failure congestive
  5. Dizziness
not specified:
  1. Breathing difficulty
  2. Weakness
  3. Fatigue (feeling of tiredness)
  4. Nausea (feeling of having an urge to vomit)
  5. Fall

Top conditions involved for these people *:

  1. Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 3,301 people, 8.44%
  2. Primary Pulmonary Hypertension (primary high blood pressure that affects the arteries in the lungs and the right side of your heart): 1,919 people, 4.91%
  3. High Blood Cholesterol : 1,892 people, 4.84%
  4. Pain : 1,792 people, 4.58%
  5. Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 1,640 people, 4.20%

Top co-used drugs for these people *:

  1. Aspirin (3,423 people, 8.76%)
  2. Coumadin (3,275 people, 8.38%)
  3. Synthroid (3,067 people, 7.85%)
  4. Lipitor (2,847 people, 7.28%)
  5. Digoxin (2,825 people, 7.23%)

* Some reports may have incomplete information.

FDA reports used in this study

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