Related topic: Scleroderma, Atelectasis
Review: could Scleroderma cause Atelectasis?
We study 859 people who have Scleroderma from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
How are my drugs for patients like me? On eHealthMe, you can find the answer by studying 348 million drug outcomes from FDA and social media. Start now >>>
Scleroderma (latest reports from 10,782 patients) is typically treated by Plaquenil, Cellcept.
Atelectasis (partial or complete collapse of the lung) (latest reports from 120,774 patients) has been reported by people with multiple myeloma, osteoporosis, pain, high blood pressure, depression.
On Apr, 12, 2014: No report is found.
You can also:
Common treatments for Scleroderma and their efficacy:
Could your drug cause it?
Comments from related studies:
From this study (5 months ago):
feeling cold improved after coming off valsartan
From this study (6 months ago):
I am running fever with shortness of breath and chest pain
From this study (1 year ago):
Would like to know if Cellcept caused the bladder infection after 1wk. of use.I was taking 500mg a day for treatment of recently diagnosed scleroderma.
Post a new comment OR Read more comments
Can you answer these questions (what is this?):
More questions for: Scleroderma, Atelectasis
More reviews for: Scleroderma, Atelectasis
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.