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Hydrocodone Compound, Tri-sprintec, Citalopram Hydrobromide drug interaction: Breast tenderness

This is a real world study of Breast tenderness (Breast pain) among people who take Hydrocodone Compound, Tri-sprintec, Citalopram Hydrobromide. The study is created by eHealthMe based on reports from FDA and social media.

What are the drugs

Hydrocodone compound (latest outcomes from 459 users) has active ingredients of homatropine methylbromide; hydrocodone bitartrate. It is often used in pain.

Tri-sprintec (latest outcomes from 530 users) has active ingredients of ethinyl estradiol; norgestimate. It is often used in birth control.

Citalopram hydrobromide (latest outcomes from 24,896 users) has active ingredients of citalopram hydrobromide. It is often used in depression.

On Dec, 19, 2014: 1 people reported to have Breast Tenderness when taking Hydrocodone Compound, Tri-sprintec, Citalopram Hydrobromide is studied.

Trend of Breast tenderness in Hydrocodone Compound, Tri-sprintec, Citalopram Hydrobromide

Gender of people who have Breast tenderness when taking the drugs * :

FemaleMale
Breast tenderness0%100%

Age of people who have Breast tenderness when taking the drugs * :

0-12-910-1920-2930-3940-4950-5960+
Breast tenderness0%0%0%0%0%100%0%0%

Severity of Breast tenderness when taking the drugs ** :

n/a

How people recovered from Breast tenderness ** :

n/a

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

More about the drug combination: Hydrocodone Compound, Tri-sprintec, Citalopram Hydrobromide drug interactions

You can also:

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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