Vasotec and Abdominal sepsis - from FDA reports


Abdominal sepsis is reported only by a few people who take Vasotec. We study 14,324 people who have side effects while taking Vasotec from FDA. Among them, 2 have Abdominal sepsis. Find out below who they are, when they have Abdominal sepsis and more.

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 Oct, 21, 2018

14,324 people reported to have side effects when taking Vasotec.
Among them, 2 people (0.01%) have Abdominal sepsis


Number of reports submitted per year:

Could Vasotec cause Abdominal sepsis?

Time on Vasotec when people have Abdominal sepsis *:

  • < 1 month: 0.0 %
  • 1 - 6 months: 0.0 %
  • 6 - 12 months: 0.0 %
  • 1 - 2 years: 0.0 %
  • 2 - 5 years: 0.0 %
  • 5 - 10 years: 100 %
  • 10+ years: 0.0 %

Gender of people who have Abdominal sepsis when taking Vasotec *:

  • female: 0.0 %
  • male: 100 %

Age of people who have Abdominal sepsis when taking Vasotec *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 0.0 %
  • 40-49: 0.0 %
  • 50-59: 0.0 %
  • 60+: 100 %

Top conditions involved for these people *:

  1. Joint Pain: 2 people, 100.00%
  2. High Blood Cholesterol: 2 people, 100.00%

Top co-used drugs for these people *:

  1. Vioxx: 2 people, 100.00%
  2. Relafen: 2 people, 100.00%
  3. Prevacid: 2 people, 100.00%
  4. Lipitor: 2 people, 100.00%
  5. Ziac: 1 person, 50.00%

Click here to view more results or personalize the results to your gender and age

Top other side effects for these people *:

  1. Wound Infection: 2 people, 100.00%
  2. Hiatal Hernia (hernia resulting from the protrusion of part of the stomach through the diaphragm): 2 people, 100.00%
  3. Miosis (constriction of the pupil of the eye, resulting from a normal response to an increase in light): 2 people, 100.00%
  4. Vasospasm (sudden constriction of a blood vessel, reducing its diameter and flow rate): 2 people, 100.00%
  5. Large Intestine Perforation (hole in large intestine): 2 people, 100.00%

Click here to view more results or personalize the results to your gender and age

* Approximation only. Some reports may have incomplete information.

FDA reports used in this study



Do you have Abdominal sepsis while taking Vasotec?


You are not alone:




Related studies

Vasotec

Vasotec has active ingredients of enalapril maleate. It is often used in high blood pressure. (latest outcomes from Vasotec 14,554 users)

Abdominal sepsis

Abdominal sepsis (abdominal infection) has been reported by people with high blood pressure, crohn's disease, rheumatoid arthritis, acne, atrial fibrillation/flutter (latest reports from 784 Abdominal sepsis patients).


Drugs that are associated with Abdominal sepsis
Abdominal sepsis (511 drugs)
Could your condition cause Abdominal sepsis
Abdominal sepsis (341 conditions)
Vasotec side effects
Browse all side effects of Vasotec
a b c d e f g h i j k l m n o p q r s t u v w x y z

What would happen?

Predict new side effects and undetected conditions when you take Vasotec and have Abdominal sepsis


Recent updates

Recent general studies
Recent personal studies

NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT 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!