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Strattera, Tylenol, Advil drug interaction: Hypoglycaemia

Hypoglycaemia: deficiency of glucose in the bloodstream.

This is a real world study of Hypoglycaemia (Hypoglycemia) among people who take Strattera, Tylenol, Advil. The study is created by eHealthMe based on 50 reports from FDA and social media.

What are the drugs

Strattera (latest outcomes from 19,169 users) has active ingredients of atomoxetine hydrochloride. It is often used in attention deficit hyperactivity disorder.

Tylenol (latest outcomes from 55,646 users) has active ingredients of acetaminophen. It is often used in pain.

Advil (latest outcomes from 22,827 users) has active ingredients of ibuprofen. It is often used in pain.

On May, 22, 2015: 50 people reported to have Hypoglycaemia when taking Strattera, Tylenol, Advil are studied.

Trend of Hypoglycaemia in Strattera, Tylenol, Advil

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


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


Severity of Hypoglycaemia when taking the drugs ** :


How people recovered from Hypoglycaemia ** :


* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

More about the drug combination: Strattera, Tylenol, Advil 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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