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Review: Okra side effects

In this review, we analyze Okra side effects by the time on the drug, gender and age (0-60+) of the people who have side effects while taking Okra. The review is based on reports from FDA and social media, and is updated regularly.

Get connected: join a mobile support group for people who have Okra side effects >>>

What is Okra

Okra (latest outcomes) has active ingredients of ambrette.

It can also be called: Ambrette, Abelmoschus Moschatus, Abelmosk, Ambretta, Ambrette Plant, Egyptian Alcee, Gandapura, Kasturidana, Kasturilatika, Latakasthuri, Latakasturi, Lata Kasturi, Lathakasthuri, Muskadana, Muskmallow, Musk-Mallow, Musk Seed, Target-Leaved Hibiscus, Tindisha.

On Oct, 13, 2014: 0 people who reported to have side effects when taking Okra is studied. Please check back later.

Most common side effects over time * :

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Most common side effects by gender * :

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Most common side effects by age * :

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* Some reports may have incomplete information.

Browse Okra side effects from A to Z:

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.

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Studies of common Okra drug interactions:

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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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