Review: could Scleroderma cause Atelectasis?
We study 862 people who have Scleroderma from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
Scleroderma (hard skin) (latest reports from 10,872 patients) can be treated by Plaquenil, Cellcept.
Atelectasis (partial or complete collapse of the lung) (latest reports from 121,902 patients) has been reported by people with multiple myeloma, osteoporosis, pain, high blood pressure, depression.
On Aug, 21, 2014: No report is found.
Do you have Scleroderma and Atelectasis?
Comments from related studies:
From this study (2 weeks ago):
I have the crest variation of scleroderma. Since developing this illness in 2004 I have developed bone spurs on both feet, as well as my right hip and my right shoulder. I am just curious if Scleroderma and or any of the above medications induce bone spurs. Thank you. Shirley
From this study (10 months ago):
feeling cold improved after coming off valsartan
From this study (11 months ago):
I am running fever with shortness of breath and chest pain
Post a new comment OR Read more comments
Can you answer these questions (what is this?):
More questions for: Scleroderma, Atelectasis
You may be interested at these reviews (what is this?):
- Developed systemic scleroderma while on copaxone for 10 yrs.
I just tested positive for both crest and systemic scleroderma. I already have ms and have been on copaxone over 10 yrs. I believe copaxone may have caused this. I dont blame the makers. I am sure it has helped more then hurt, but I wonder if this has happened to others. If so it should be something ...
More reviews for: Scleroderma, Atelectasis
Common treatments for Scleroderma and their efficacy:
Could your drug cause it?
Studies of common Scleroderma symptoms:
Atelectasis related symptom studies:
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.