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From FDA reports: drug interactions between Granisetron, Amlodipine, Decadron, Halaven for a Female patient aged 76

This is a personalized study for a 76 year old female patient. The study is created by eHealthMe based on reports of 34 people who take the same drugs and have drug interactionsfrom FDA.

On Jul, 24, 2014: 34 people who reported to have interactions when taking Granisetron, Amlodipine, Decadron, Halaven are studied

Trend of Granisetron, Amlodipine, Decadron, Halaven's drug interactions, side effects, and effectiveness reports (8148630)

Information of the patient in this study:

Age: 76

Gender: female

Conditions: Prophylaxis, Metastases To Lung, Breast Cancer Recurrent, Hypertension

Drugs taking:
- Granisetron
- Granisetron
- Amlodipine
- Decadron
- Amlodipine
- Halaven
- Decadron
- Halaven
- Amlodipine

Drug interactions have: Dizziness, Malaise

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 76 (±5):

InteractionNumber of reports
Dizziness2 (100.00%)
Malaise (a feeling of general discomfort or uneasiness)2 (100.00%)

Most common interactions experienced by females aged 76 (±5) in the use of Granisetron, Amlodipine, Decadron, Halaven:

InteractionNumber of reports
Pyrexia (fever)2
Dizziness2
Malaise (a feeling of general discomfort or uneasiness)2
White Blood Cell Count Decreased2
Neutrophil Count Decreased (less than normal number of neutrophil a type of blood cell)2

Most common interactions experienced by females aged 76 (±5) in long term use of Granisetron, Amlodipine, Decadron, Halaven:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Dizziness4 (11.76%)
Malaise (a feeling of general discomfort or uneasiness)8 (23.53%)

Most common interactions experienced by people in the use of Granisetron, Amlodipine, Decadron, Halaven:

InteractionNumber of reports
Neutropenia (an abnormally low number of neutrophils)34
Pneumonia34
Leukopenia (less number of white blood cells in blood)34
Lymphopenia (an abnormally low level of lymphocytes in the blood)32
Febrile Neutropenia (fever with reduced white blood cells)30
White Blood Cell Count Decreased16
Paronychia (infection in the tissues adjacent to a nail on a finger or toe)16
Malnutrition (condition that results from eating a diet in which certain nutrients are lacking)16
Dehydration (dryness resulting from the removal of water)16
Oesophagitis (inflammation of oesophagus)16

Most common interactions experienced by people in long term use of Granisetron, Amlodipine, Decadron, Halaven:

InteractionNumber of reports
Deep Vein Thrombosis (blood clot in a major vein that usually develops in the legs and/or pelvis)3
Supraventricular Tachycardia (rapid heart rhythm originating at or above the atrioventricular node)3
Renal Impairment (severely reduced kidney function)3
Anuria (failure of the kidneys to produce urine)3
Endocarditis Noninfective (an inflammation of the inner layer of the heart noninfective)3
C-reactive Protein Increased3
Pulmonary Embolism (blockage of the main artery of the lung)3
Haematuria (presence of blood in urine)3
Disseminated Intravascular Coagulation (systemic activation of blood coagulation)3
Rash Erythematous (redness of the skin)3

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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