Who have Babesiosis with Benadryl - from FDA reports


There is no Babesiosis reported by people who take Benadryl yet. This review analyzes which people have Babesiosis with Benadryl. It is created by eHealthMe based on reports from FDA, and is updated regularly.

How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.


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On Feb, 21, 2019

No report is found.

Do you have Babesiosis while taking Benadryl?


You are not alone:




Related studies

Benadryl

Benadryl has active ingredients of diphenhydramine hydrochloride. It is often used in allergies. (latest outcomes from Benadryl 57,530 users)

Babesiosis

Babesiosis (malaria-like parasitic disease caused by infection with babesia) has been reported by people with multiple sclerosis, rheumatoid arthritis, pain, neuropathy peripheral, burkitt lymphoma (latest reports from 282 Babesiosis patients).


Drugs that are associated with Babesiosis
Babesiosis
Could your condition cause Babesiosis
Babesiosis
Benadryl side effects

Browse by gender and age

Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+


Browse all side effects of Benadryl
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Compare Benadryl to similar drugs:


What would happen?

Predict new side effects and undetected conditions when you take Benadryl and have Babesiosis




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NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT 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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