Who have Quartan malaria with Keflex - from FDA reports


There is no Quartan malaria reported by people who take Keflex yet. This review analyzes which people have Quartan malaria with Keflex. 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.



On Jan, 22, 2019

No report is found.

Do you have Quartan malaria while taking Keflex?


You are not alone:




Related studies

Keflex

Keflex has active ingredients of cephalexin. It is often used in infection. (latest outcomes from Keflex 10,824 users)

Quartan Malaria

Quartan malaria (an infectious disease characterized by cycles of chills, fever, and sweating, caused by a protozoan of the genus plasmodium in red blood cells) has been reported by people with malaria, hiv infection, onchocerciasis, chronic myeloid leukaemia, preventive health care (latest reports from 4,558 Quartan malaria patients).


Drugs that are associated with Quartan malaria
Quartan malaria
Could your condition cause Quartan malaria
Quartan malaria
Keflex 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 Keflex
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What would happen?

Predict new side effects and undetected conditions when you take Keflex and have Quartan malaria




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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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