Review: could Candesartan Cilexetil cause Atherosclerosis?


Summary

Atherosclerosis is found among people who take Candesartan Cilexetil, especially for people who are female, 60+ old also take medication Furosemide, and have Atrial fibrillation . We study 5,726 people who have side effects while taking Candesartan cilexetil from FDA and social media. Among them, 15 have Atherosclerosis. Find out below who they are, when they have Atherosclerosis and more.

Personalized health information

On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>

Candesartan Cilexetil

Candesartan cilexetil has active ingredients of candesartan cilexetil. It is often used in high blood pressure. (latest outcomes from Candesartan cilexetil 6,546 users)

Atherosclerosis

Atherosclerosis (disorder of the arteries) has been reported by people with muscle aches, rashes, itching, skin blushing/flushing, fatigue (latest reports from 11,896 Atherosclerosis patients).

On Sep, 22, 2016

5,726 people reported to have side effects when taking Candesartan Cilexetil.
Among them, 15 people (0.26%) have Atherosclerosis


Number of reports submitted per year:

Could Candesartan cilexetil cause Atherosclerosis?

Gender of people who have Atherosclerosis when taking Candesartan Cilexetil *:

  • female: 53.33 %
  • male: 46.67 %

Age of people who have Atherosclerosis when taking Candesartan Cilexetil *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 0.0 %
  • 40-49: 6.67 %
  • 50-59: 0.0 %
  • 60+: 93.33 %

Top conditions involved for these people *:

  • Vitamin Supplementation (3 people, 20.00%)
  • Hyperphosphataemia (3 people, 20.00%)
  • Blood Glucose Increased (3 people, 20.00%)
  • Blood Cholesterol Increased (3 people, 20.00%)
  • Atrial Fibrillation (3 people, 20.00%)

Top co-used drugs for these people *:

  • Prednisolone (8 people, 53.33%)
  • Furosemide (8 people, 53.33%)
  • Lansoprazole (6 people, 40.00%)
  • Latanoprost (4 people, 26.67%)
  • Alendronic Acid (4 people, 26.67%)

Top other side effects for these people *:

  • Vomiting (4 people, 26.67%)
  • Syncope (4 people, 26.67%)
  • Duodenal Ulcer Haemorrhage (4 people, 26.67%)
  • Circulatory Collapse (4 people, 26.67%)
  • Aortic Calcification (4 people, 26.67%)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

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

Do you have Atherosclerosis when taking Candesartan cilexetil?

Browse all side effects of Candesartan cilexetil

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

Drugs that are associated with Atherosclerosis

Atherosclerosis

Could your condition cause Atherosclerosis

Atherosclerosis

Related studies


Recent conversations of related support groups:

Can you answer these questions?

More questions for: Candesartan cilexetil, Atherosclerosis

You may be interested in these reviews

More reviews for: Candesartan cilexetil, Atherosclerosis


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.