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From FDA reports: drug interactions between Plavix, Beta-channgel Blockers, Glyceryl Trinitrate for a Male patient aged 77

This is a personalized study of Plavix, Beta-channgel Blockers, Glyceryl Trinitrate drug interactions for a 77 year old male patient. The study is created by eHealthMe based on 558 people who take the drugs and have drug interactions.

On Mar, 13, 2014: 558 people who reported to have interactions when taking Plavix, Beta-channgel Blockers, Glyceryl Trinitrate are studied

Trend of Plavix, Beta-channgel Blockers, Glyceryl Trinitrate's drug interactions, side effects, and effectiveness reports (2444526)

Information of the patient in this study:

Age: 77

Gender: male

Conditions: Retinal Vascular Thrombosis

Drugs taking:
- Plavix
- Plavix
- Beta-channgel Blockers
- Glyceryl Trinitrate

Drug interactions have: Abdominal Pain, Blood Glucose Increased, Lipase Increased, Nausea, Pancreatitis, Vomiting

eHealthMe real world results:

Comparison with this patient's adverse outcomes among males aged 77 (±5):

InteractionNumber of reports
Abdominal Pain2 (2.53%)
Blood Glucose Increased8 (10.13%)
Lipase Increased1 (1.27%)
Nausea (feeling of having an urge to vomit)5 (6.33%)
Pancreatitis (inflammation of pancreas)3 (3.80%)
Vomiting10 (12.66%)

Most common interactions experienced by males aged 77 (±5) in the use of Plavix, Beta-channgel Blockers, Glyceryl Trinitrate:

InteractionNumber of reports
Diarrhoea22
Pyrexia (fever)16
Neutropenia (an abnormally low number of neutrophils)16
Dehydration (dryness resulting from the removal of water)9
Blood Glucose Increased8
Hypotension (abnormally low blood pressure)6
Food Poisoning (poison in food)6
Malaise (a feeling of general discomfort or uneasiness)6
Large Intestine Perforation (hole in large intestine)5
Gastrointestinal Haemorrhage (bleeding gastrointestinal tract)5

Most common interactions experienced by males aged 77 (±5) in long term use of Plavix, Beta-channgel Blockers, Glyceryl Trinitrate:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Abdominal Pain12 (2.15%)
Blood Glucose Increased16 (2.87%)
Lipase Increased1 (0.18%)
Nausea (feeling of having an urge to vomit)45 (8.06%)
Pancreatitis (inflammation of pancreas)4 (0.72%)
Vomiting54 (9.68%)

Most common interactions experienced by people in the use of Plavix, Beta-channgel Blockers, Glyceryl Trinitrate:

InteractionNumber of reports
Asthenia (weakness)170
Dyspnoea (difficult or laboured respiration)152
Anxiety135
Myocardial Infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)112
Dysphagia (condition in which swallowing is difficult or painful)110
Hypotension (abnormally low blood pressure)96
Pain88
Renal Failure Chronic (long lasting kidney dysfunction)64
Osteomyelitis (infection of bone)55
Sepsis (a severe blood infection that can lead to organ failure and death)55

Most common interactions experienced by people in long term use of Plavix, Beta-channgel Blockers, Glyceryl Trinitrate:

InteractionNumber of reports
Cerebrovascular Accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture)1
Drug Ineffective1
Haemoglobin Decreased1
Haemorrhage (bleeding)1
Rectal Haemorrhage (bleeding from anus)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.

Related topic: Abdominal Pain, Blood Glucose Increased, Lipase Increased, Nausea, Pancreatitis, Plavix, Retinal Vascular Thrombosis, Vomiting

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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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