A study for a 59 year old woman who takes Toprol-Xl, Requip, Metformin, Synthroid, Neurontin - from FDA reports

107 females aged 59 (±5) who take the same drugs are studied. This is a personalized study for a 59 year old female patient who has Tachycardia, Diabetes, Restless Legs, Hypothyroid, Diabetic Neuropathy. The study is created by eHealthMe based on reports from FDA.

How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.

Who is eHealthMe: we are a data analysis company who specializes in health care industry. Our original studies have been referenced on 500+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and EANO. On eHealthMe, you can research drugs and monitor them (see testimonials).

On Jul, 15, 2018

107 females aged 59 (±5) who take Toprol-Xl, Requip, Metformin, Synthroid, Neurontin are studied.

Number of reports submitted per year:

Toprol-Xl, Requip, Metformin, Synthroid, Neurontin for a 59-year old woman.

Information of the patient in this study:

  • Age: 59
  • Gender: female
  • Conditions: Tachycardia, Diabetes, Restless Legs, Hypothyroid, Diabetic Neuropathy
  • Drugs taken:
    • Toprol-Xl (metoprolol succinate)
    • Metformin (metformin hydrochloride)
    • Requip (ropinirole hydrochloride)
    • Synthroid (levothyroxine sodium)
    • Neurontin (gabapentin)

eHealthMe real world results:

Comparison with this patient's adverse outcomes:

  • Hyperreflexia(overactive or over responsive reflexes): 0 (0% of females aged 59 (±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 - 6 months:
6 - 12 months:
1 - 2 years:
  1. Renal impairment (severely reduced kidney function)
2 - 5 years:
5 - 10 years:
10+ years:
not specified:
  1. Cardiac failure congestive
  2. Weakness
  3. Chronic obstructive pulmonary disease (a progressive disease that makes it hard to breathe)
  4. Mitral valve incompetence (inefficient heart valve)
  5. Injury

Top conditions involved for these people *:

  1. Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 15 people, 14.02%
  2. High Blood Cholesterol : 15 people, 14.02%
  3. Depression : 11 people, 10.28%
  4. Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 10 people, 9.35%
  5. Stress And Anxiety : 9 people, 8.41%

Top co-used drugs for these people *:

  1. Nexium (23 people, 21.50%)
  2. Lantus (22 people, 20.56%)
  3. Lisinopril (21 people, 19.63%)
  4. Lipitor (20 people, 18.69%)
  5. Lyrica (18 people, 16.82%)

* Some reports may have incomplete information.

FDA reports used in this study

You are not alone:

What are the drugs?

What are the conditions?

What are the symtoms?

Could your drugs cause:

Could your conditions cause:

Related studies:

Related publications that referenced our studies

Recent updates

General studies

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.