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From FDA reports: drug interactions between Lexapro, Demerol

This is a real world study of Lexapro, Demerol drug interactions. The study is created by eHealthMe based on 179 people who take the drugs and have drug interactions.

Information of the patient in this study:

Drugs taking:
- Lexapro
- Demerol

Drug interactions have: Drug Interaction, Drug Level Increased, Respiratory Failure

On Jan, 28, 2014: 179 people who reported to have interactions when taking Lexapro, Demerol are studied

Trend of Lexapro, Demerol's drug interactions, side effects, and effectiveness reports (723529)

eHealthMe real world results:

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Drug Interaction6 (3.35%)
Drug Level Increased1 (0.56%)
Respiratory Failure (inadequate gas exchange by the respiratory system)21 (11.73%)

Most common interactions experienced by people in the use of Lexapro, Demerol:

InteractionNumber of reports
Anxiety115
Asthenia (weakness)88
Vomiting78
Pain62
Abdominal Pain49
Osteoarthritis (a joint disease caused by cartilage loss in a joint)40
Injury40
Osteonecrosis Of Jaw (death of bone of jaw)39
Bronchitis (inflammation of the mucous membrane in the bronchial tubes)37
Nausea (feeling of having an urge to vomit)36

Most common interactions experienced by people in long term use of Lexapro, Demerol:

None.

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: Demerol, Drug Level Increased, Lexapro, Respiratory Failure

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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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