Will you have Family stress with Add - from FDA reports


Family stress is found among people with Add, especially for people who are male, 10-19 old, take medication Strattera and have Adverse drug reaction. This study is created by eHealthMe based on reports of 14 people who have Add from FDA, and is updated regularly.

What's eHealthMe?

eHealthMe is a health data analysis company based in Mountain View, California. eHealthMe monitors and analyzes the outcomes of drugs and supplements that are currently on the market. The results are readily available to health care professionals and consumers.

eHealthMe has released original studies on market drugs and worked with leading universities and institutions such as IBM, London Health Science Centre, Mayo Clinic, Northwestern University and VA. eHealthMe studies have now been referenced in over 500 peer-reviewed medical publications.

How we gather our data?

Healthcare data is obtained from a number of sources including the Food and Drug Administration (FDA). This information is aggregated and used to produce personalized reports that patients can reference.

The information that eHealthMe collects includes:

  • Side effects (including severity and how people recover from them)
  • Associated conditions or symptoms
  • Drug effectiveness
  • Demographic data regarding drug use

How the study uses the data?

The study is based on Family stress and Add, and their synonyms.

What is Add?

Add (attention deficit disorder-difficult to define) can be treated by Abilify, Adderall, Adderall 10, Adderall 12.5, Adderall 15 (latest reports from 81,785 Add patients)

What is Family stress?

Family stress has been reported by people with indigestion, abdominal distension, depression, osteoporosis, pain (latest reports from 3,234 Family stress patients).

How to use the study?

Patients can bring a copy of the report to their healthcare provider to ensure that all drug risks and benefits are fully discussed and understood. It is recommended that patients use the information presented as a part of a broader decision-making process.

On Mar, 14, 2019

14 people who have Add and Family Stress are studied.

Number of reports submitted per year:

Would you have Family stress when you have Add?

Gender of people who have Add and experience Family Stress *:

  • female: 30.77 %
  • male: 69.23 %

Age of people who have Add and experience Family Stress *:

  • 0-1: 0.0 %
  • 2-9: 18.18 %
  • 10-19: 72.73 %
  • 20-29: 0.0 %
  • 30-39: 9.09 %
  • 40-49: 0.0 %
  • 50-59: 0.0 %
  • 60+: 0.0 %

Top co-existing conditions for these people *:

  1. Stress And Anxiety: 1 person, 7.14%
  2. Insomnia (sleeplessness): 1 person, 7.14%
  3. Drug Dependence: 1 person, 7.14%
  4. Depression: 1 person, 7.14%
  5. Adverse Drug Reaction: 1 person, 7.14%

Most common drugs for these people *:

  1. Strattera: 5 people, 35.71%
  2. Vyvanse: 2 people, 14.29%
  3. Effexor: 2 people, 14.29%
  4. Adderall: 2 people, 14.29%
  5. Zolpidem: 1 person, 7.14%
  6. Seasonale: 1 person, 7.14%
  7. Prozac: 1 person, 7.14%
  8. Invega Trinza: 1 person, 7.14%
  9. Invega Sustenna: 1 person, 7.14%
  10. Intuniv: 1 person, 7.14%

Top symptoms for these people *:

  1. Suicide Attempt: 4 people, 28.57%
  2. Abnormal Behavior: 3 people, 21.43%
  3. Impulsive Behavior: 3 people, 21.43%
  4. Intentional Self-Injury: 3 people, 21.43%
  5. Educational Problem: 3 people, 21.43%
  6. Suicidal Ideation: 2 people, 14.29%
  7. Stress And Anxiety: 2 people, 14.29%
  8. Headache (pain in head): 2 people, 14.29%
  9. Aggression: 2 people, 14.29%
  10. Irritability: 2 people, 14.29%

* Approximation only. Some reports may have incomplete information.

Do you have Family stress with Add?

You are not alone:

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What would happen?

Predict new side effects and undetected conditions when you have Family stress and Add

Recent updates

Recent general studies
Recent personal studies

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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).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.