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From FDA reports: drug interactions between Vytorin, Ketoconazole for a Female patient aged 60

This is a personalized study for a 60 year old female patient. The study is created by eHealthMe based on reports of 27 people who take the same drugs and have drug interactionsfrom FDA.

On Sep, 27, 2014: 27 people who reported to have interactions when taking Vytorin, Ketoconazole are studied

Trend of Vytorin, Ketoconazole's drug interactions, side effects, and effectiveness reports (930507)

Information of the patient in this study:

Age: 60

Gender: female

Conditions: Blood Cholesterol Increased

Drugs taking:
- Vytorin: used for 1 - 6 months
- Ketoconazole

Drug interactions have: Rhabdomyolysis

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 60 (±5):

InteractionNumber of reports
Rhabdomyolysis (a condition in which damaged skeletal muscle tissue breaks down)1 (100.00%)

Most common interactions experienced by females aged 60 (±5) in the use of Vytorin, Ketoconazole:

InteractionNumber of reports
Rhabdomyolysis (a condition in which damaged skeletal muscle tissue breaks down)1

Most common interactions experienced by females aged 60 (±5) in long term use of Vytorin, Ketoconazole:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Rhabdomyolysis (a condition in which damaged skeletal muscle tissue breaks down)16 (59.26%)

Most common interactions experienced by people in the use of Vytorin, Ketoconazole:

InteractionNumber of reports
Renal Failure Acute (rapid kidney dysfunction)18
Rhabdomyolysis (a condition in which damaged skeletal muscle tissue breaks down)16
Drug Interaction14
Confusional State12
Fall12
Blood Cholesterol Increased11
Diabetes Mellitus Inadequate Control10
Hyperlipidaemia (presence of excess lipids in the blood)10
Type 2 Diabetes Mellitus10
Weight Increased10

Most common interactions experienced by people in long term use of Vytorin, Ketoconazole:

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.

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NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also considered.

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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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