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Diazepam, Concerta, Risperdal, Depakote for a 16-year old boy

This is a study of Diazepam, Concerta, Risperdal, Depakote for a 16 year old male patient who has Aggression, ADHD, Autism Spectrum Disorder. The study is created by eHealthMe based on 3 male patients aged 16 (±5) who take the drugs from FDA and social media.

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Information of the patient in this study:

Age: 12

Gender: male

Conditions: Aggression, ADHD, Autism Spectrum Disorder

Drugs taking:
- Diazepam (diazepam)
- Concerta (methylphenidate hydrochloride)
- Risperdal (risperidone)
- Depakote (divalproex sodium)

On Feb, 1, 2014: 3 males aged 12 (±5) who reported to have interactions when taking Diazepam, Concerta, Risperdal, Depakote are studied

Trend of Diazepam, Concerta, Risperdal, Depakote's drug interactions, side effects and effectiveness reports (3166501)

Most common interactions experienced by males aged 12 (±5) in the use of Diazepam, Concerta, Risperdal, Depakote:

InteractionNumber of reports
Somnolence (a state of near-sleep, a strong desire for sleep)3
Memory Impairment3
Agitation (state of anxiety or nervous excitement)3
Disturbance In Attention2
Aggression2
Headache (pain in head)2
Weight Increased2
Constipation2
Anger2
Drug Ineffective2

Most common interactions experienced by males aged 12 (±5) in long term use of Diazepam, Concerta, Risperdal, Depakote:

None.

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, Aggression, Autism Spectrum Disorder, Concerta, Depakote, Diazepam, Risperdal

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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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- Attention deficit hyperactivity disorder
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