Who have Shunt occlusion with Ambien - from FDA reports


Shunt occlusion is reported only by a few people who take Ambien. We study 69,739 people who have side effects while taking Ambien from FDA. Among them, 5 have Shunt occlusion. Find out below who they are, when they have Shunt occlusion 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.


Peer to Peer mobile support

Peer support for this study is available on our Ginger Health app. It's free, anonymous and secure. The app is ideal for people taking multiple medications or having multiple conditions.



On Feb, 10, 2019

69,739 people reported to have side effects when taking Ambien.
Among them, 5 people (0.01%) have Shunt occlusion


Number of reports submitted per year:

Could Ambien cause Shunt occlusion?

Gender of people who have Shunt occlusion when taking Ambien *:

  • female: 0.0 %
  • male: 100 %

Age of people who have Shunt occlusion when taking Ambien *:

  • 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. Arthritis (form of joint disorder that involves inflammation of one or more joints): 5 people, 100.00%

Top co-used drugs for these people *:

  1. Vioxx: 5 people, 100.00%
  2. Tenormin: 5 people, 100.00%
  3. Procardia Xl: 5 people, 100.00%
  4. Pravachol: 5 people, 100.00%
  5. Glucophage: 5 people, 100.00%

Top other side effects for these people *:

  1. Weakness: 5 people, 100.00%
  2. Hypovolaemia (a decreased volume of circulating blood in the body): 5 people, 100.00%
  3. Head Injury: 5 people, 100.00%
  4. Gastritis (inflammation of stomach): 5 people, 100.00%
  5. Gait Disturbance: 5 people, 100.00%
  6. Fall: 5 people, 100.00%
  7. Fainting (loss of consciousness and postural tone): 5 people, 100.00%
  8. Enlarged Prostate: 5 people, 100.00%
  9. Dyspnea Exertional: 5 people, 100.00%
  10. Duodenitis (inflammation of the duodenum): 5 people, 100.00%

* Approximation only. Some reports may have incomplete information.

Do you have Shunt occlusion while taking Ambien?


You are not alone:




Related studies

Ambien

Ambien has active ingredients of zolpidem tartrate. It is often used in insomnia. (latest outcomes from Ambien 75,817 users)

Shunt occlusion

Shunt occlusion (blockage of shunt) has been reported by people with hyperparathyroidism secondary, renal failure chronic, high blood pressure, nephrogenic anaemia, preventive health care (latest reports from 388 Shunt occlusion patients).


Drugs that are associated with Shunt occlusion
Shunt occlusion (190 drugs)
Could your condition cause Shunt occlusion
Shunt occlusion (102 conditions)
Ambien 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 Ambien
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 Ambien to similar drugs:

Related publications that referenced our studies


What would happen?

Predict new side effects and undetected conditions when you take Ambien and have Shunt occlusion


FDA reports used in this study



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!