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From FDA reports: drug interactions between Parnate, Levothyroxine Sodium, Provigil, Ambien for a Female patient aged 64

This is a personalized study for a 64 year old female patient. The study is created by eHealthMe based on reports of 177 people who take the same drugs and have drug interactionsfrom FDA.

On Nov, 21, 2014: 177 people who reported to have interactions when taking Parnate, Levothyroxine Sodium, Provigil, Ambien are studied

Trend of Parnate, Levothyroxine Sodium, Provigil, Ambien's drug interactions, side effects, and effectiveness reports (2736660)

Information of the patient in this study:

Age: 64

Gender: female

Conditions: Depression

Drugs taking:
- Parnate
- Levothyroxine Sodium
- Provigil
- Ambien

Drug interactions have: Blood Testosterone Decreased, Dizziness, Feeling Abnormal, Laboratory Test Abnormal, Orthostatic Hypotension, Pain

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 64 (±5):

InteractionNumber of reports
Blood Testosterone Decreased2 (5.26%)
Dizziness6 (15.79%)
Feeling Abnormal4 (10.53%)
Laboratory Test Abnormal2 (5.26%)
Orthostatic Hypotension (a medical condition consisting of a sudden decrease in blood pressure when a person stands up)16 (42.11%)
Pain38 (100.00%)

Most common interactions experienced by females aged 64 (±5) in the use of Parnate, Levothyroxine Sodium, Provigil, Ambien:

InteractionNumber of reports
Anxiety38
Pain38
Toothache (tooth pain)36
Anhedonia (inability to experience pleasure from activities usually found enjoyable)36
Injury36
Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)34
Fall34
Urinary Tract Infection33
Tooth Fracture32
Fatigue (feeling of tiredness)30

Most common interactions experienced by females aged 64 (±5) in long term use of Parnate, Levothyroxine Sodium, Provigil, Ambien:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Blood Testosterone Decreased2 (1.13%)
Dizziness35 (19.77%)
Feeling Abnormal4 (2.26%)
Laboratory Test Abnormal4 (2.26%)
Orthostatic Hypotension (a medical condition consisting of a sudden decrease in blood pressure when a person stands up)16 (9.04%)
Pain152 (85.88%)

Most common interactions experienced by people in the use of Parnate, Levothyroxine Sodium, Provigil, Ambien:

InteractionNumber of reports
Anxiety177
Nausea (feeling of having an urge to vomit)176
Pain152
Chest Pain144
Gastrooesophageal Reflux Disease (stomach contents (food or liquid) leak backwards from the stomach into the oesophagus)128
Back Pain128
Osteonecrosis Of Jaw (death of bone of jaw)128
Fatigue (feeling of tiredness)122
Dyspepsia (indigestion)122
Vomiting118

Most common interactions experienced by people in long term use of Parnate, Levothyroxine Sodium, Provigil, Ambien:

InteractionNumber of reports
Intentional Overdose4
Completed Suicide (act of taking one's own life)4
Depression4
Anxiety4
Suicide Attempt4
Mental Disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability)4
Memory Impairment2
Hepatic Failure (liver failure)2
Epilepsy (common and diverse set of chronic neurological disorders characterized by seizures)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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