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From FDA reports: drug interactions between Imitrex, Ibuprofen, Naproxen, Soma, Trazodone Hcl, Oxycodone Hcl for a Female patient aged 47

This is a personalized study for a 47 year old female patient. The study is created by eHealthMe based on reports of 8 people who take the same drugs and have drug interactionsfrom FDA.

On Aug, 17, 2014: 8 people who reported to have interactions when taking Imitrex, Ibuprofen, Naproxen, Soma, Trazodone Hcl, Oxycodone Hcl are studied

Trend of Imitrex, Ibuprofen, Naproxen, Soma, Trazodone Hcl, Oxycodone Hcl's drug interactions, side effects, and effectiveness reports (3181062)

Information of the patient in this study:

Age: 47

Gender: female

Conditions: Migraine

Drugs taking:
- Imitrex
- Ibuprofen
- Naproxen
- Soma
- Trazodone Hcl
- Oxycodone Hcl

Drug interactions have: Overdose, Nausea, Drug Dispensing Error, Dizziness, Accidental Overdose

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 47 (±5):

InteractionNumber of reports
Overdose2 (50.00%)
Nausea (feeling of having an urge to vomit)4 (100.00%)
Drug Dispensing Error2 (50.00%)
Dizziness4 (100.00%)
Accidental Overdose3 (75.00%)

Most common interactions experienced by females aged 47 (±5) in the use of Imitrex, Ibuprofen, Naproxen, Soma, Trazodone Hcl, Oxycodone Hcl:

InteractionNumber of reports
Headache (pain in head)4
Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)4
Abdominal Pain4
Nausea (feeling of having an urge to vomit)4
Back Pain4
Dizziness4
Muscle Spasms (muscle contraction)4
Intervertebral Disc Disorder (spinal disc disorder)4
Hypomagnesaemia (electrolyte disturbance in which there is an abnormally low level of magnesium in the blood)4
Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development)4

Most common interactions experienced by females aged 47 (±5) in long term use of Imitrex, Ibuprofen, Naproxen, Soma, Trazodone Hcl, Oxycodone Hcl:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Overdose2 (25.00%)
Nausea (feeling of having an urge to vomit)8 (100.00%)
Drug Dispensing Error2 (25.00%)
Dizziness8 (100.00%)
Accidental Overdose3 (37.50%)

Most common interactions experienced by people in the use of Imitrex, Ibuprofen, Naproxen, Soma, Trazodone Hcl, Oxycodone Hcl:

InteractionNumber of reports
Nausea (feeling of having an urge to vomit)8
Dizziness8
Dehydration (dryness resulting from the removal of water)8
Gastroenteritis (inflammation of stomach and intestine)8
Pelvic Pain6
Vision Blurred6
Headache (pain in head)6
Tremor (trembling or shaking movements in one or more parts of your body)6
Abdominal Pain6
Back Pain6

Most common interactions experienced by people in long term use of Imitrex, Ibuprofen, Naproxen, Soma, Trazodone Hcl, Oxycodone Hcl:

InteractionNumber of reports
Gastroenteritis (inflammation of stomach and intestine)1
Dehydration (dryness resulting from the removal of water)1

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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