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Review: Rhus toxicodendron side effects

In this review, we analyze Rhus toxicodendron side effects by the time on the drug, gender and age (0-60+) of the people who have side effects while taking Rhus toxicodendron. The review is based on 3 people who have side effects while taking Rhus toxicodendron from FDA and social media, and is updated regularly.

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What is Rhus toxicodendron

Rhus toxicodendron (latest outcomes) has active ingredients of poison ivy.

It can also be called: Poison Ivy, Markweed, Poison Vine, Rhus radicans, Rhus Tox, Three-Leafed Ivy, Toxicodendron pubescens, Toxicodendron quercifolium, Toxicodendron radicans, Toxicodendron toxicarium.

On Jul, 23, 2014: 3 people who reported to have side effects when taking Rhus toxicodendron are studied


Most common side effects over time * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ yearsnot specified
Stomach Discomfortn/an/an/an/an/an/aCarotid Artery Occlusion
Transient Ischaemic Attack

Most common side effects by gender * :

Carotid Artery OcclusionStomach Discomfort
Transient Ischaemic Attack

Most common side effects by age * :

n/an/an/aStomach Discomfortn/an/an/aCarotid Artery Occlusion
Transient Ischaemic Attack

* Some reports may have incomplete information.

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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.

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DISCLAIMER: All material available on 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 or 1-800-FDA-1088 (1-800-332-1088).

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