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From FDA reports: drug interactions between Concerta, Risperidone, Depakote for a Male patient aged 10

This is a personalized study for a 10 year old male patient. The study is created by eHealthMe based on reports of 95 people who take the same drugs and have drug interactionsfrom FDA.

On Nov, 14, 2014: 95 people who reported to have interactions when taking Concerta, Risperidone, Depakote are studied

Trend of Concerta, Risperidone, Depakote's drug interactions, side effects, and effectiveness reports (2853301)

Information of the patient in this study:

Age: 10

Gender: male

Conditions: Attention Deficit/hyperactivity Disorder, Bipolar Disorder

Drugs taking:
- Concerta
- Risperidone
- Depakote
- Depakote

Drug interactions have: Anticonvulsant Drug Level Increased, Aortic Dilatation, Bipolar Disorder, Cardiac Murmur, Heart Valve Calcification, Hypoaesthesia, Mental Status Changes

eHealthMe real world results:

Comparison with this patient's adverse outcomes among males aged 10 (±5):

InteractionNumber of reports
Anticonvulsant Drug Level Increased2 (5.41%)
Aortic Dilatation2 (5.41%)
Bipolar Disorder (mood disorder)4 (10.81%)
Cardiac Murmur (an heart sound in valve abnormality)2 (5.41%)
Heart Valve Calcification (deposits of calcium (calcification) in parts of the valve)2 (5.41%)
Hypoaesthesia (reduced sense of touch or sensation)2 (5.41%)
Mental Status Changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation)6 (16.22%)

Most common interactions experienced by males aged 10 (±5) in the use of Concerta, Risperidone, Depakote:

InteractionNumber of reports
Aggression14
Agitation (state of anxiety or nervous excitement)14
Tardive Dyskinesia (a disorder that involves involuntary movements)12
Weight Increased12
Drug Ineffective10
Dystonia (abnormal muscle tone)9
Drug Interaction Nos8
Rash (redness)8
Somnolence (a state of near-sleep, a strong desire for sleep)6
Condition Aggravated (worse condition)6

Most common interactions experienced by males aged 10 (±5) in long term use of Concerta, Risperidone, Depakote:

None.

For people in general (regardless of gender or age):

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Anticonvulsant Drug Level Increased2 (2.11%)
Aortic Dilatation2 (2.11%)
Bipolar Disorder (mood disorder)6 (6.32%)
Cardiac Murmur (an heart sound in valve abnormality)2 (2.11%)
Heart Valve Calcification (deposits of calcium (calcification) in parts of the valve)2 (2.11%)
Hypoaesthesia (reduced sense of touch or sensation)2 (2.11%)
Mental Status Changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation)12 (12.63%)

Most common interactions experienced by people in the use of Concerta, Risperidone, Depakote:

InteractionNumber of reports
Aggression42
Weight Increased38
Type 2 Diabetes Mellitus36
Suicidal Ideation34
Abnormal Behaviour28
Tardive Dyskinesia (a disorder that involves involuntary movements)28
Diabetes Mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)26
Depression25
Anger24
Drug Ineffective20

Most common interactions experienced by people in long term use of Concerta, Risperidone, Depakote:

InteractionNumber of reports
Self-injurious Ideation4
Anger4
Suicidal Ideation4
Depression4
Weight Increased4
Diabetes Mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)4
Aggression4
Polydipsia (excessive thirst)2
Suicide Attempt2
Pyrexia (fever)2

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.

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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