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From FDA reports: drug interactions between Livalo, Cozaar for a Female patient aged 82

This is a personalized study for a 82 year old female patient. The study is created by eHealthMe based on reports of 46 people who take the same drugs and have drug interactionsfrom FDA.

On Oct, 26, 2014: 46 people who reported to have interactions when taking Livalo, Cozaar are studied

Trend of Livalo, Cozaar's drug interactions, side effects, and effectiveness reports (3405653)

Information of the patient in this study:

Age: 82

Gender: female

Conditions: Dyslipidaemia

Drugs taking:
- Livalo
- Cozaar: used for 2 - 5 years

Drug interactions have: Rhabdomyolysis

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 82 (±5):

InteractionNumber of reports
Rhabdomyolysis (a condition in which damaged skeletal muscle tissue breaks down)2 (40.00%)

Most common interactions experienced by females aged 82 (±5) in the use of Livalo, Cozaar:

InteractionNumber of reports
Cerebral Haemorrhage Traumatic (bleeding in brain due to injury)4
Subdural Haematoma (blood collects between the skull and the surface of the brain)4
Road Traffic Accident4
Brain Contusion (a form of traumatic brain injury)4
Haemorrhage Subcutaneous (bleeding from skin)4
Neutropenia (an abnormally low number of neutrophils)4
Rhabdomyolysis (a condition in which damaged skeletal muscle tissue breaks down)2

Most common interactions experienced by females aged 82 (±5) in long term use of Livalo, Cozaar:

InteractionNumber of reports
Cerebral Haemorrhage Traumatic (bleeding in brain due to injury)2
Subdural Haematoma (blood collects between the skull and the surface of the brain)2
Brain Contusion (a form of traumatic brain injury)2
Haemorrhage Subcutaneous (bleeding from skin)2
Road Traffic Accident2

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)2 (4.35%)

Most common interactions experienced by people in the use of Livalo, Cozaar:

InteractionNumber of reports
Pyrexia (fever)12
Hepatic Function Abnormal12
Neutropenia (an abnormally low number of neutrophils)12
Sudden Hearing Loss10
Hyphaema (collection of blood inside the front part of the eye)10
Leukopenia (less number of white blood cells in blood)10
Gamma-glutamyltransferase Increased8
Thrombocytopenia (decrease of platelets in blood)8
Condition Aggravated (worse condition)8
Blood Pressure Increased6

Most common interactions experienced by people in long term use of Livalo, Cozaar:

InteractionNumber of reports
Subdural Haematoma (blood collects between the skull and the surface of the brain)3
Haemorrhage Subcutaneous (bleeding from skin)3
Road Traffic Accident3
Brain Contusion (a form of traumatic brain injury)3
Cerebral Haemorrhage Traumatic (bleeding in brain due to injury)3
Lymphadenopathy Mediastinal (an enlargement of the lymph nodes in the part of the chest that separates the lungs)2
Renal Cyst (kidney cyst)2
Renal Failure (kidney dysfunction)2
Haemodialysis2
Renal Atrophy (wasting of kidney)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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