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Review: Tenex, Flexeril for a 35-year old woman

This is a personalized study of taking Tenex, Flexeril for a 35 year old female patient who has ADHD. The study is created by eHealthMe based on reports from FDA and social media.

Information of the patient in this study:

Age: 31

Gender: female

Conditions: ADHD

Drugs taking:
- Tenex (guanfacine hydrochloride)

On Jan, 20, 2014: 1 female aged 31 (±5) who reported to have interactions when taking Tenex, Flexeril is studied

Trend of Tenex, Flexeril's drug interactions, side effects and effectiveness reports (3412385)

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
among females aged 31 (±5) who take the drugs
FlexerilThe drug has been added in the study. Outcomes of the drug mix are shown.

Most common interactions experienced by females aged 31 (±5) in the use of Tenex, Flexeril:

InteractionNumber of reports
Weight Increased1

Most common interactions experienced by females aged 31 (±5) in long term use of Tenex, Flexeril:

InteractionNumber of reports
Weight Increased1

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.

Related topic: ADHD, Flexeril, Tenex

You can also:

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Drug effectiveness in real world:

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Comments from related studies:

  • From this study (1 week ago):

  • At least once a month I am experience a bloody show. Premenstrual symptoms have been severely escalated (severe irritability, rage, night terrors, and insomnia).

    Reply

  • From this study (3 weeks ago):

  • Pervasive developmental disorder...autism...unexplained g.i. Issues with multiple procedures only finding inflammation...prescribed sucralfate after severe vomiting which seemed to help for awhile, but cycle seems to be starting all over again...vomits often after eating

    Reply

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

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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).

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