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A study for a 47-year old woman who takes Coumadin, Lactulose

Summary: 61 female patients aged 47 (±5) who take the same drugs are studied.

This is a personalized study for a 47 year old female patient who has DVT, Constipation. The study is created by eHealthMe based on reports from FDA and social media.

 

On Mar, 31, 2015: 61 females aged 47 (±5) who take Coumadin, Lactulose are studied

Coumadin, Lactulose outcomes

Information of the patient in this study:

Age: 47

Gender: female

Conditions: DVT, Constipation

Drugs taking:
- Coumadin (warfarin sodium): used for 10+ years
- Lactulose - 10GM/15ML (lactulose): used for < 1 month

eHealthMe real world results:

Drug effectiveness over time :

n/a

Most common drug interactions over time * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ yearsnot specified
Peripheral IschaemiaCalciphylaxisn/an/an/an/an/aUrinary Tract Infection
Vaginal HaemorrhageProteinuriaFatigue
International Normalised Ratio IncreasedMyocardial IschaemiaAbdominal Pain
HaematemesisCardiac FailureBack Pain
Injury
Mass
Neuropathy Peripheral
Rectal Haemorrhage
Chest Pain
Bone Disorder

* Some reports may have incomplete information.

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.

You can also:

 

 

 

You are not alone! Join a related mobile support group on :
- support group for people who have Constipation
- support group for people who have DVT
- support group for people who take Coumadin
- support group for people who take Lactulose

Recent related drug studies (Check your drugs):

Related drug interaction studies:

Drug effectiveness in real world:

Complete drug side effects:

Alternative drugs:

NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also 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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