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From FDA reports: drug interactions between Neulasta, Herceptin, Claritin-d, Taxotere, Cytoxan

This is a study of Neulasta, Herceptin, Claritin-d, Taxotere, Cytoxan drug interactions. The study is created by eHealthMe based on reports of 2 people who take the same drugs and have drug interactionsfrom FDA.

On Sep, 5, 2014: 2 people who reported to have interactions when taking Neulasta, Herceptin, Claritin-d, Taxotere, Cytoxan are studied

Trend of Neulasta, Herceptin, Claritin-d, Taxotere, Cytoxan's drug interactions, side effects, and effectiveness reports (2503240)

Information of the patient in this study:

Gender: female

Conditions: Chemotherapy

Drugs taking:
- Neulasta: used for 1 - 6 months
- Herceptin
- Claritin-d
- Taxotere: used for 1 - 6 months
- Cytoxan: used for 1 - 6 months

Drug interactions have: Leukopenia

eHealthMe real world results:

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Leukopenia (less number of white blood cells in blood)2 (100.00%)

Most common interactions experienced by people in the use of Neulasta, Herceptin, Claritin-d, Taxotere, Cytoxan:

InteractionNumber of reports
White Blood Cell Count Decreased2
Leukopenia (less number of white blood cells in blood)2

Most common interactions experienced by people in long term use of Neulasta, Herceptin, Claritin-d, Taxotere, Cytoxan:

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.

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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