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From FDA reports: drug interactions between Lisinopril, Furosemide for a Male patient aged 75

This is a personalized study for a 75 year old male patient. The study is created by eHealthMe based on reports of 18,975 people who take the same drugs and have drug interactionsfrom FDA.

On Aug, 21, 2014: 18,975 people who reported to have interactions when taking Lisinopril, Furosemide are studied

Trend of Lisinopril, Furosemide's drug interactions, side effects, and effectiveness reports (867063)

Information of the patient in this study:

Age: 75

Gender: male

Conditions: Blood Pressure

Drugs taking:
- Lisinopril: used for 1 - 6 months
- Furosemide: used for 1 - 2 years

Drug interactions have: Orthostatic Hypotension

eHealthMe real world results:

Comparison with this patient's adverse outcomes among males aged 75 (±5):

InteractionNumber of reports
Orthostatic Hypotension (a medical condition consisting of a sudden decrease in blood pressure when a person stands up)20 (0.76%)

Most common interactions experienced by males aged 75 (±5) in the use of Lisinopril, Furosemide:

InteractionNumber of reports
Anxiety710
Dyspnoea (difficult or laboured respiration)667
Renal Failure (kidney dysfunction)611
Atrial Fibrillation (fibrillation of the muscles of the atria of the heart)586
Pain536
Cardiac Failure Congestive488
Hypotension (abnormally low blood pressure)480
Renal Failure Acute (rapid kidney dysfunction)428
Nausea (feeling of having an urge to vomit)396
Injury367

Most common interactions experienced by males aged 75 (±5) in long term use of Lisinopril, Furosemide:

InteractionNumber of reports
Bradycardia (abnormally slow heart action)42
Cardiac Failure36
Malaise (a feeling of general discomfort or uneasiness)34
Renal Impairment (severely reduced kidney function)32
Renal Failure Acute (rapid kidney dysfunction)30
Toxicity To Various Agents (poisoning due to various agents)22
Mental Status Changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation)22
Condition Aggravated (worse condition)22
Renal Failure (kidney dysfunction)21
Drug Interaction14

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Orthostatic Hypotension (a medical condition consisting of a sudden decrease in blood pressure when a person stands up)146 (0.77%)

Most common interactions experienced by people in the use of Lisinopril, Furosemide:

InteractionNumber of reports
Dyspnoea (difficult or laboured respiration)5,816
Anxiety5,606
Pain4,430
Asthenia (weakness)4,399
Cardiac Failure Congestive3,952
Nausea (feeling of having an urge to vomit)3,338
Fatigue (feeling of tiredness)2,879
Renal Failure Acute (rapid kidney dysfunction)2,754
Anaemia (lack of blood)2,691
Oedema Peripheral (superficial swelling)2,648

Most common interactions experienced by people in long term use of Lisinopril, Furosemide:

InteractionNumber of reports
Anxiety125
Renal Failure Acute (rapid kidney dysfunction)106
Renal Failure (kidney dysfunction)86
Cardiac Failure Congestive68
Depression68
Injury66
Pain56
Nausea (feeling of having an urge to vomit)50
Emotional Distress48
Cardiac Failure46

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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