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Could Metoprolol Succinate, Vicodin Hp together cause Dyspnoea?

Dyspnoea: difficult or laboured respiration.

This is a real world study of Dyspnoea (Breathing difficulty) among people who take Metoprolol Succinate, Vicodin Hp. The study is created by eHealthMe based on 706 reports from FDA and social media.

What are the drugs

Metoprolol succinate (latest outcomes from 18,034 users) has active ingredients of metoprolol succinate. It is often used in high blood pressure.

Vicodin hp (latest outcomes from 208 users) has active ingredients of acetaminophen; hydrocodone bitartrate. It is often used in pain.

On Nov, 24, 2014: 3,784 people reported to have side effects when taking Metoprolol Succinate, Vicodin Hp. Among them, 706 people (18.66%) have Dyspnoea.

Trend of Dyspnoea in Metoprolol Succinate, Vicodin Hp

Gender of people who have Dyspnoea when taking the drugs * :


Age of people who have Dyspnoea when taking the drugs * :


Severity of Dyspnoea when taking the drugs ** :


How people recovered from Dyspnoea ** :


* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

More about the drug combination: Metoprolol Succinate, Vicodin Hp 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 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 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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