Hydrocele and Idiopathic hypertrophic subaortic stenosis - from FDA reports


There is no Idiopathic Hypertrophic Subaortic Stenosis reported by people with Hydrocele yet. We study people who have Idiopathic Hypertrophic Subaortic Stenosis and Hydrocele from FDA. Find out below who they are, other conditions they have and drugs they take.



On Jul, 17, 2018

No report is found.

What's next: manage your medications




Related studies


Hydrocele

Hydrocele (latest reports from 1,046 Hydrocele patients)

Idiopathic Hypertrophic Subaortic Stenosis

Idiopathic hypertrophic subaortic stenosis (primary heart enlargement with or without presence of left ventricular outflow tract (lvot) obstruction) has been reported by people with high blood pressure, glycogen storage disease type ii, osteoporosis, neoplasm malignant, metastases to spine (latest reports from 1,549 Idiopathic hypertrophic subaortic stenosis patients).


Drugs that are associated with Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis (365 drugs)
Other conditions that could cause Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis (566 conditions)
Browse all symptoms of Hydrocele
a b c d e f g h i j k l m n o p q r s t u v w x y z

You are not alone. Join our personalized support groups:

You may be interested in these posts

More posts for: Hydrocele, Idiopathic hypertrophic subaortic stenosis

Recent updates

General studies
Active Support Groups
Latest posts

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.