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From FDA reports: drug interactions between Extavia, Motrin, Provigil, Zanaflex 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 6 people who take the same drugs and have drug interactionsfrom FDA.

On Sep, 2, 2014: 6 people who reported to have interactions when taking Extavia, Motrin, Provigil, Zanaflex are studied

Trend of Extavia, Motrin, Provigil, Zanaflex's drug interactions, side effects, and effectiveness reports (8493777)

Information of the patient in this study:

Age: 43

Gender: female

Conditions: Multiple Sclerosis

Drugs taking:
- Extavia
- Motrin
- Provigil
- Zanaflex

Drug interactions have: Contusion, Headache, Optic Neuritis, Haemorrhage, Vision Blurred, Pain In Extremity, Injection Site Reaction, Multiple Sclerosis Relapse, Pyrexia, Eye Pain

eHealthMe real world results:

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

InteractionNumber of reports
Contusion (a type of hematoma of tissue in which capillaries)5 (100.00%)
Headache (pain in head)5 (100.00%)
Optic Neuritis (optic nerve inflammation)5 (100.00%)
Haemorrhage (bleeding)5 (100.00%)
Vision Blurred5 (100.00%)
Pain In Extremity5 (100.00%)
Injection Site Reaction5 (100.00%)
Multiple Sclerosis Relapse (reoccurrence of a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath)5 (100.00%)
Pyrexia (fever)5 (100.00%)
Eye Pain5 (100.00%)

Most common interactions experienced by females aged 43 (±5) in the use of Extavia, Motrin, Provigil, Zanaflex:

InteractionNumber of reports
Pyrexia (fever)5
Contusion (a type of hematoma of tissue in which capillaries)5
Multiple Sclerosis Relapse (reoccurrence of a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath)5
Haemorrhage (bleeding)5
Injection Site Reaction5
Optic Neuritis (optic nerve inflammation)5
Pain In Extremity5
Eye Pain5
Vision Blurred5
Headache (pain in head)5

Most common interactions experienced by females aged 43 (±5) in long term use of Extavia, Motrin, Provigil, Zanaflex:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Contusion (a type of hematoma of tissue in which capillaries)6 (100.00%)
Headache (pain in head)6 (100.00%)
Optic Neuritis (optic nerve inflammation)6 (100.00%)
Haemorrhage (bleeding)6 (100.00%)
Vision Blurred6 (100.00%)
Pain In Extremity6 (100.00%)
Injection Site Reaction6 (100.00%)
Multiple Sclerosis Relapse (reoccurrence of a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath)6 (100.00%)
Pyrexia (fever)6 (100.00%)
Eye Pain6 (100.00%)

Most common interactions experienced by people in the use of Extavia, Motrin, Provigil, Zanaflex:

InteractionNumber of reports
Pyrexia (fever)6
Contusion (a type of hematoma of tissue in which capillaries)6
Injection Site Reaction6
Multiple Sclerosis Relapse (reoccurrence of a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath)6
Haemorrhage (bleeding)6
Optic Neuritis (optic nerve inflammation)6
Eye Pain6
Headache (pain in head)6
Vision Blurred6
Pain In Extremity6

Most common interactions experienced by people in long term use of Extavia, Motrin, Provigil, Zanaflex:

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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