A study for a 46 year old woman who takes Simvastatin, Droxia, Lantus, Acetylsalicylic Acid, Actos - from FDA reports


8 females aged 46 (±5) who take the same drugs are studied. This is a personalized study for a 46 year old female patient who has High Cholesterol, Sickle Cell Anemia, Pain, Diabetes. The study is created by eHealthMe based on reports from FDA.

How the study uses the data?

The study is based on gender, age, active ingredients of any drugs used. Other drugs that have the same active ingredients (e.g. generic drugs) are considered.

What are the drugs?

What are the conditions?

What are the symtoms?

How to use the study?

Patients can bring a copy of the report to their healthcare provider to ensure that all drug risks and benefits are fully discussed and understood. It is recommended that patients use the information presented as a part of a broader decision-making process.

On Dec, 05, 2018

8 females aged 46 (±5) who take Simvastatin, Droxia, Lantus, Acetylsalicylic Acid, Actos are studied.

Number of reports submitted per year:

Simvastatin, Droxia, Lantus, Acetylsalicylic Acid, Actos for a 46-year old woman.

Information of the patient in this study:

  • Age: 46
  • Gender: female
  • Conditions: High Cholesterol, Sickle Cell Anemia, Pain, Diabetes
  • Drugs taken:
    • Simvastatin (simvastatin)
    • Droxia (hydroxyurea)
    • Lantus (insulin glargine recombinant)
    • Acetylsalicylic Acid (aspirin)
    • Actos (pioglitazone hydrochloride)

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

  • Gastroparesis(delayed emptying of food from the stomach): 0 (0% of females aged 46 (±5) who take the drugs)

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 drug interactions over time

< 1 month:
  1. Weight decreased
  2. Muscle aches (muscle pain)
  3. Nausea (feeling of having an urge to vomit)
  4. Blood glucose increased
  5. Fatigue (feeling of tiredness)
  6. Feeling cold
  7. Hepatic steatosis (fatty liver disease)
  8. Liver function test abnormal
  9. Glycosylated haemoglobin increased
  10. Blood glucose decreased
1 - 6 months:
  1. Blood glucose increased
  2. Chest pain
6 - 12 months:
1 - 2 years:
2 - 5 years:
5 - 10 years:
10+ years:
not specified:
  1. Blood glucose increased
  2. Fatigue (feeling of tiredness)
  3. Urinary tract infection
  4. Diabetic ketoacidosis (diabetic ketoacidosis (dka) is high concentrations of ketone bodies)
  5. Diabetic neuropathy (neuropathic disorders that are associated with diabetes mellitus)
  6. Diabetic foot
  7. Nausea (feeling of having an urge to vomit)
  8. Sepsis syndrome (a clinical condition of blood infection)
  9. Chest pain
  10. Hyperglycemia (high blood sugar)

Top conditions involved for these people *:

  1. Sleep Disorder : 3 people, 37.50%
  2. Stress And Anxiety : 2 people, 25.00%
  3. Panic Disorder : 2 people, 25.00%
  4. Insomnia (sleeplessness): 2 people, 25.00%
  5. Quit Smoking : 1 person, 12.50%
  6. Muscle Spasms (muscle contraction): 1 person, 12.50%
  7. Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 1 person, 12.50%
  8. Insulin-Requiring Type 2 Diabetes Mellitus : 1 person, 12.50%
  9. Gastric Ulcer (stomach ulcer): 1 person, 12.50%
  10. Depression : 1 person, 12.50%

Top co-used drugs for these people *:

  1. Lisinopril (4 people, 50.00%)
  2. Cymbalta (3 people, 37.50%)
  3. Seroquel (3 people, 37.50%)
  4. Zyrtec (2 people, 25.00%)
  5. Plavix (2 people, 25.00%)
  6. Prevacid (2 people, 25.00%)
  7. Novolog (2 people, 25.00%)
  8. Fish Oil (2 people, 25.00%)
  9. Clonidine (2 people, 25.00%)
  10. Reglan (2 people, 25.00%)

* Some reports may have incomplete information.

What is next?

You are not alone:

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FDA reports used in this study

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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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