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From FDA reports: drug interactions between Suboxone, Prozac, Neurontin, Fluoxetine, Alprazolam, Zyprexa, Ventolin Hfa for a Female patient aged 43

This is a personalized study for a 43 year old female patient. The study is created by eHealthMe based on reports of 3 people who take the same drugs and have drug interactionsfrom FDA.

On Jul, 6, 2014: 3 people who reported to have interactions when taking Suboxone, Prozac, Neurontin, Fluoxetine, Alprazolam, Zyprexa, Ventolin Hfa are studied

Trend of Suboxone, Prozac, Neurontin, Fluoxetine, Alprazolam, Zyprexa, Ventolin Hfa's drug interactions, side effects, and effectiveness reports (822986)

Information of the patient in this study:

Age: 43

Gender: female

Conditions: Drug Dependence

Drugs taking:
- Suboxone: used for < 1 month
- Prozac
- Neurontin
- Fluoxetine
- Alprazolam
- Zyprexa
- Ventolin Hfa

Drug interactions have: Death

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 43 (±5):

InteractionNumber of reports
Death2 (100.00%)

Most common interactions experienced by females aged 43 (±5) in the use of Suboxone, Prozac, Neurontin, Fluoxetine, Alprazolam, Zyprexa, Ventolin Hfa:

InteractionNumber of reports
Blood Triglycerides Increased2
Diabetes Mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)2
Diabetic Coma (diabetic ketoacidosis (dka) is high concentrations of ketone bodies)2
Polyneuropathy Idiopathic Progressive (progressive disorder that affects the peripheral nerves and has no identifiable primary cause)2
Polyneuropathy (neurological disorder that occurs when many peripheral nerves throughout the body malfunction simultaneously)2
Premature Menopause2
Neuropathy Peripheral (surface nerve damage)2
Diabetic Foot2
Paraesthesia (sensation of tingling, tickling, prickling, pricking, or burning of a person's skin with no apparent long-term physical effect)2
Pseudodementia (severe form of depression that results from a progressive brain disorder in which cognitive changes mimic those of dementia)2

Most common interactions experienced by females aged 43 (±5) in long term use of Suboxone, Prozac, Neurontin, Fluoxetine, Alprazolam, Zyprexa, Ventolin Hfa:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Death2 (66.67%)

Most common interactions experienced by people in the use of Suboxone, Prozac, Neurontin, Fluoxetine, Alprazolam, Zyprexa, Ventolin Hfa:

InteractionNumber of reports
Diabetes Mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)3
Blood Triglycerides Increased3
Diabetic Coma (diabetic ketoacidosis (dka) is high concentrations of ketone bodies)3
Hyperglycaemia (high blood sugar)3
Pseudodementia (severe form of depression that results from a progressive brain disorder in which cognitive changes mimic those of dementia)2
Premature Menopause2
Paraesthesia (sensation of tingling, tickling, prickling, pricking, or burning of a person's skin with no apparent long-term physical effect)2
Neuropathy Peripheral (surface nerve damage)2
Diabetic Foot2
Polyneuropathy Idiopathic Progressive (progressive disorder that affects the peripheral nerves and has no identifiable primary cause)2

Most common interactions experienced by people in long term use of Suboxone, Prozac, Neurontin, Fluoxetine, Alprazolam, Zyprexa, Ventolin Hfa:

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.

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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