Who have Nocturia with Terazosin hydrochloride - from FDA reports


Nocturia is found among people who take Terazosin hydrochloride, especially for people who are male, 60+ old , have been taking the drug for < 1 month, also take medication Lupron Depot, and have High blood cholesterol. This study is created by eHealthMe based on reports of 1,287 people who have side effects when taking Terazosin hydrochloride from FDA, and is updated regularly.

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


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On Feb, 10, 2019

1,287 people reported to have side effects when taking Terazosin hydrochloride.
Among them, 6 people (0.47%) have Nocturia


Number of reports submitted per year:

Could Terazosin hydrochloride cause Nocturia?

Time on Terazosin hydrochloride when people have Nocturia *:

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

Gender of people who have Nocturia when taking Terazosin hydrochloride *:

  • female: 0.0 %
  • male: 100 %

Age of people who have Nocturia when taking Terazosin hydrochloride *:

  • 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. Prostatomegaly (enlargement of the prostate): 1 person, 16.67%
  2. Prostate Cancer: 1 person, 16.67%
  3. High Blood Cholesterol: 1 person, 16.67%

Top co-used drugs for these people *:

  1. Zocor: 1 person, 16.67%
  2. Vioxx: 1 person, 16.67%
  3. Verapamil Hydrochloride: 1 person, 16.67%
  4. Vantas: 1 person, 16.67%
  5. Theophylline: 1 person, 16.67%
  6. Simvastatin: 1 person, 16.67%
  7. Ranitidine: 1 person, 16.67%
  8. Niaspan: 1 person, 16.67%
  9. Monopril: 1 person, 16.67%
  10. Lupron Depot: 1 person, 16.67%

Top other side effects for these people *:

  1. Drug Ineffective: 2 people, 33.33%
  2. White Blood Cell Count Decreased: 1 person, 16.67%
  3. Urine Flow Decreased: 1 person, 16.67%
  4. Dehydration (dryness resulting from the removal of water): 1 person, 16.67%
  5. Disseminated Intravascular Coagulation (systemic activation of blood coagulation): 1 person, 16.67%
  6. Enterococcal Bacteraemia (presence of bacteria lactic acid in the blood): 1 person, 16.67%
  7. Fever: 1 person, 16.67%
  8. Haematuria Present (presence of blood in urine due to trauma): 1 person, 16.67%
  9. Haemoglobin Decreased: 1 person, 16.67%
  10. Loin Pain (pain originates from kidney): 1 person, 16.67%

* Approximation only. Some reports may have incomplete information.

Do you have Nocturia while taking Terazosin hydrochloride?


You are not alone:




Related studies

Terazosin hydrochloride

Terazosin hydrochloride has active ingredients of terazosin hydrochloride. It is often used in prostate examination abnormal. (latest outcomes from Terazosin hydrochloride 1,678 users)

Nocturia

Nocturia (the need to get up in the night to urinate) has been reported by people with osteoporosis, high blood pressure, enlarged prostate, high blood cholesterol, pain (latest reports from 9,884 Nocturia patients).


Drugs that are associated with Nocturia
Nocturia (1,433 drugs)
Could your condition cause Nocturia
Nocturia (884 conditions)
Terazosin hydrochloride side effects

Browse by gender and age

Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+


Browse all side effects of Terazosin hydrochloride
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

Compare Terazosin hydrochloride to similar drugs:


What would happen?

Predict new side effects and undetected conditions when you take Terazosin hydrochloride and have Nocturia


FDA reports used in this study



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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.

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