Spironolactone and hydrochlorothiazide and Arf - from FDA reports

Arf is reported only by a few people who take Spironolactone And Hydrochlorothiazide. We study 164 people who have side effects while taking Spironolactone and hydrochlorothiazide from FDA. Among them, 5 have Arf. Find out below who they are, when they have Arf 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, 19, 2018

164 people reported to have side effects when taking Spironolactone and hydrochlorothiazide.
Among them, 5 people (3.05%) have Arf

Number of reports submitted per year:

Could Spironolactone and hydrochlorothiazide cause Arf?

Gender of people who have Arf when taking Spironolactone and hydrochlorothiazide *:

  • female: 40 %
  • male: 60 %

Age of people who have Arf when taking Spironolactone and hydrochlorothiazide *:

Top conditions involved for these people *:

  1. Type 2 Diabetes: 1 person, 20.00%
  2. Oedema (fluid collection in tissue): 1 person, 20.00%
  3. Mitral Valve Replacement: 1 person, 20.00%
  4. Dementia Alzheimer's Type (loss of mental ability with alzheimer's symptom): 1 person, 20.00%
  5. Back Pain: 1 person, 20.00%

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

Top co-used drugs for these people *:

  1. Trasylol: 2 people, 40.00%
  2. Nitroglycerin: 2 people, 40.00%
  3. Heparin: 2 people, 40.00%
  4. Warfarin Sodium: 1 person, 20.00%
  5. Carvedilol: 1 person, 20.00%

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

Top other side effects for these people *:

  1. Stress And Anxiety: 2 people, 40.00%
  2. Nausea (feeling of having an urge to vomit): 2 people, 40.00%
  3. Depression: 2 people, 40.00%
  4. Injury: 2 people, 40.00%
  5. Emotional Distress: 2 people, 40.00%

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 Arf while taking Spironolactone and hydrochlorothiazide?

You are not alone:

Related studies

Spironolactone and hydrochlorothiazide

Spironolactone and hydrochlorothiazide has active ingredients of hydrochlorothiazide; spironolactone. It is often used in swelling. (latest outcomes from Spironolactone and hydrochlorothiazide 179 users)


Arf (acute renal failure (arf), is a rapid loss of kidney) has been reported by people with high blood pressure, multiple myeloma, diabetes, coronary artery bypass, rheumatoid arthritis (latest reports from 100,462 Arf patients).

Drugs that are associated with Arf
Arf (2,908 drugs)
Could your condition cause Arf
Arf (3,030 conditions)
Spironolactone and hydrochlorothiazide side effects
Browse all side effects of Spironolactone and hydrochlorothiazide
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 Spironolactone and hydrochlorothiazide and have Arf

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...


Thank you!