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From FDA reports: drug interactions between Amiodarone, Amoxicillin And Clavulanate Potassium for a Male patient aged 79

This is a personalized study for a 79 year old male patient. The study is created by eHealthMe based on reports of 625 people who take the same drugs and have drug interactionsfrom FDA.

On Dec, 9, 2014: 625 people who reported to have interactions when taking Amiodarone, Amoxicillin And Clavulanate Potassium are studied

Trend of Amiodarone, Amoxicillin And Clavulanate Potassium's drug interactions, side effects, and effectiveness reports (3764168)

Information of the patient in this study:

Age: 79

Gender: male

Conditions: Osteitis

Drugs taking:
- Amiodarone
- Amoxicillin And Clavulanate Potassium: used for < 1 month

Drug interactions have: Tubulointerstitial Nephritis, Septic Shock, Renal Failure Acute, Purpura

eHealthMe real world results:

Comparison with this patient's adverse outcomes among males aged 79 (±5):

InteractionNumber of reports
Tubulointerstitial Nephritis (a form of nephritis affecting the interstitium of the kidneys surrounding the tubules)6 (4.76%)
Septic Shock (shock due to blood infection)4 (3.17%)
Renal Failure Acute (rapid kidney dysfunction)8 (6.35%)
Purpura (purplish discoloration of the skin)6 (4.76%)

Most common interactions experienced by males aged 79 (±5) in the use of Amiodarone, Amoxicillin And Clavulanate Potassium:

InteractionNumber of reports
Drug Interaction49
Renal Failure (kidney dysfunction)36
Blood Creatinine Increased26
Leukopenia (less number of white blood cells in blood)24
International Normalised Ratio Increased22
Prothrombin Time Shortened22
Oliguria (not enough urine)20
Cytolytic Hepatitis (dissolution or destruction of a liver cell)20
General Physical Health Deterioration (weak health status)18
Hepatic Failure (liver failure)18

Most common interactions experienced by males aged 79 (±5) in long term use of Amiodarone, Amoxicillin And Clavulanate Potassium:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Tubulointerstitial Nephritis (a form of nephritis affecting the interstitium of the kidneys surrounding the tubules)22 (3.52%)
Septic Shock (shock due to blood infection)24 (3.84%)
Renal Failure Acute (rapid kidney dysfunction)180 (28.80%)
Purpura (purplish discoloration of the skin)23 (3.68%)

Most common interactions experienced by people in the use of Amiodarone, Amoxicillin And Clavulanate Potassium:

InteractionNumber of reports
Atrial Fibrillation (fibrillation of the muscles of the atria of the heart)229
Renal Failure Acute (rapid kidney dysfunction)180
Anaemia (lack of blood)171
Drug Interaction148
Pain147
Asthenia (weakness)141
International Normalised Ratio Increased132
Oedema Peripheral (superficial swelling)128
Fall122
Thrombocytopenia (decrease of platelets in blood)118

Most common interactions experienced by people in long term use of Amiodarone, Amoxicillin And Clavulanate Potassium:

InteractionNumber of reports
Diverticulum (out pouching of a hollow (or a fluid-filled) structure in the body)1
Blood Bilirubin Increased1
Ceruloplasmin Increased1
Cholecystitis (infection of gallbladder)1
Hepatitis (inflammation of the liver)1
Vomiting1
Hyperthyroidism (over activity of the thyroid gland)1
Liver Function Test Abnormal1
Respiratory Distress (difficulty in breathing)1
Jaundice (a yellowish pigmentation of the skin, the conjunctival membranes)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.

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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