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From FDA reports: drug interactions between Daypro, Acetaminophen for a Female patient aged 69

This is a personalized study of Daypro, Acetaminophen drug interactions for a 69 year old female patient. The study is created by eHealthMe based on 165 people who take the drugs and have drug interactions.

Information of the patient in this study:

Age: 69

Gender: female

Drugs taking:
- Daypro
- Acetaminophen

Drug interactions have: Urticaria Nos

On Feb, 2, 2014: 165 people who reported to have interactions when taking Daypro, Acetaminophen are studied

Trend of Daypro, Acetaminophen's drug interactions, side effects, and effectiveness reports (1858268)

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Urticaria Nos1 (6.25%)

Most common interactions experienced by females aged 69 (±5) in the use of Daypro, Acetaminophen:

InteractionNumber of reports
Epistaxis (bleed from the nose)6
Blood Pressure Increased5
Myocardial Infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)4
Drug Effect Decreased3
Emotional Distress2
Dermatitis Exfoliative Nos2
Hepatic Disorder Nos2
Dermatitis Nos2
Duodenitis (inflammation of the duodenum)1
Heart Rate Increased1

Most common interactions experienced by females aged 69 (±5) in long term use of Daypro, Acetaminophen:

InteractionNumber of reports
Hypertension (high blood pressure)1
Myocardial Infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)1
Coronary Artery Disease (plaque building up along the inner walls of the arteries of the heart, which narrows the arteries and restricts blood flow to the heart)1
Hepatomegaly (abnormal enlargement of the liver)1
Cerebrovascular Disorder (disease of brain)1
Emotional Distress1
Inflammation1
Pulmonary Embolism (blockage of the main artery of the lung)1
Transient Ischaemic Attack (a transient episode of neurologic dysfunction caused by ischemia (loss of blood flow))1
Lymphadenopathy Mediastinal (an enlargement of the lymph nodes in the part of the chest that separates the lungs)1

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Urticaria Nos1 (0.61%)

Most common interactions experienced by people in the use of Daypro, Acetaminophen:

InteractionNumber of reports
Dyspnoea (difficult or laboured respiration)60
Erythema (redness of the skin)53
Arthralgia (joint pain)44
Chest Pain41
Pain29
Oedema Peripheral (superficial swelling)27
Urinary Tract Infection26
Cough23
Back Pain21
Pain In Extremity20

Most common interactions experienced by people in long term use of Daypro, Acetaminophen:

InteractionNumber of reports
Hypertension (high blood pressure)1
Myocardial Infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)1
Coronary Artery Disease (plaque building up along the inner walls of the arteries of the heart, which narrows the arteries and restricts blood flow to the heart)1
Hepatomegaly (abnormal enlargement of the liver)1
Cerebrovascular Disorder (disease of brain)1
Emotional Distress1
Inflammation1
Pulmonary Embolism (blockage of the main artery of the lung)1
Transient Ischaemic Attack (a transient episode of neurologic dysfunction caused by ischemia (loss of blood flow))1
Lymphadenopathy Mediastinal (an enlargement of the lymph nodes in the part of the chest that separates the lungs)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: Acetaminophen, Daypro

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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