Ramipril Vs. Choline for a female patient aged 79 - from FDA reports


This is a personalized comparison Ramipril, Choline for a woman aged 79. 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). If you find eHealthMe useful, please help us to spread the words below or leave us a testimonial.



On Jan, 08, 2019

9,357 females aged 79 (±5) who take Ramipril, Choline are studied.


Number of reports submitted per year:

Ramipril, Choline for a female patient aged 79.

Information of the patient in this study:

  • Age: 79
  • Gender: female
  • Reason for the study: Cerebrovascular Accident

Drugs in this study:

  • Ramipril (ramipril)
  • Choline (choline)

eHealthMe real world results for females aged 79 (±5):

Comparison with the specified adverse outcomes:
Outcome and its % of total reports:

Cerebrovascular Accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture):
  • Ramipril: 2.21 %
  • Choline: 0.01 %

Most common side effects:

Ramipril:
  1. Abdominal Pain
  2. Abdominal Pain Upper
  3. Acute Kidney Failure
  4. Agitation (state of anxiety or nervous excitement)
  5. Agranulocytosis (a deficiency of granulocytes in the blood, causing increased vulnerability to infection)
  6. Alanine Aminotransferase Increased
  7. Anaemia (lack of blood)
  8. Angioedema (rapid swelling of the dermis)
  9. Appetite - Decreased (decreased appetite occurs when you have a reduced desire to eat)
  10. Arrhythmias (irregular heartbeat)
Choline:
  1. Abdominal Distension
  2. Agranulocytosis (a deficiency of granulocytes in the blood, causing increased vulnerability to infection)
  3. Anaemia (lack of blood)
  4. Appetite - Decreased (decreased appetite occurs when you have a reduced desire to eat)
  5. Azotaemia (excess of urea or other nitrogenous compounds in the blood)
  6. Back Pain
  7. Blepharitis (chronic inflammation of the eyelid)
  8. Breathing Difficulty
  9. Bronchopulmonary Aspergillosis (lung disorder caused by aspergillus fungi)
  10. Burning Sensation

Most common side effects experienced by people in long term use:

Ramipril:
  1. Abdominal Discomfort
  2. Abdominal Pain
  3. Ageusia (loss of taste functions of the tongue)
  4. Agitation (state of anxiety or nervous excitement)
  5. Alanine Aminotransferase Increased
  6. Anaemia (lack of blood)
  7. Angioedema (rapid swelling of the dermis)
  8. Appetite - Decreased (decreased appetite occurs when you have a reduced desire to eat)
  9. Aspartate Aminotransferase Increased
  10. Atrioventricular Block Complete (heart block complete)
Choline:

n/a

FDA reports used in this study

What are the drugs?

What are the symptoms?

  • Cerebrovascular accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture) has been reported by people with diabetes, high blood pressure, arthritis, multiple sclerosis, pain (latest reports from 229,165 Cerebrovascular accident patients).


Related studies:

Recent updates

Recent general studies
Recent personal 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.

Submit your testimonial

  • Please fill in your Testimonial.
  • Please enter a minimum of 10 characters for your Testimonial.
  • Please fill in your Name.

Please wait...

{progressItem}

Thank you!