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From FDA reports: drug interactions between Erbitux, Carboplatin, Digoxin, Darvon, Neurontin for a Female patient aged 70

This is a personalized study for a 70 year old female patient. The study is created by eHealthMe based on reports of 2 people who take the same drugs and have drug interactionsfrom FDA.

On Aug, 27, 2014: 2 people who reported to have interactions when taking Erbitux, Carboplatin, Digoxin, Darvon, Neurontin are studied

Trend of Erbitux, Carboplatin, Digoxin, Darvon, Neurontin's drug interactions, side effects, and effectiveness reports (2503664)

Information of the patient in this study:

Age: 70

Gender: female

Conditions: Neoplasm Malignant

Drugs taking:
- Erbitux
- Carboplatin
- Digoxin
- Darvon
- Neurontin

Drug interactions have: Recall Phenomenon

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 70 (±5):

InteractionNumber of reports
Recall Phenomenon2 (100.00%)

Most common interactions experienced by females aged 70 (±5) in the use of Erbitux, Carboplatin, Digoxin, Darvon, Neurontin:

InteractionNumber of reports
Recall Phenomenon2

Most common interactions experienced by females aged 70 (±5) in long term use of Erbitux, Carboplatin, Digoxin, Darvon, Neurontin:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Recall Phenomenon2 (100.00%)

Most common interactions experienced by people in the use of Erbitux, Carboplatin, Digoxin, Darvon, Neurontin:

InteractionNumber of reports
Recall Phenomenon2

Most common interactions experienced by people in long term use of Erbitux, Carboplatin, Digoxin, Darvon, Neurontin:

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.

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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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