Upper respiratory tract infection is found among people with Systemic lupus erythematosus, especially for people who are female, 50-59 old, take medication Plaquenil and have Systemic lupus erythematosus. We study 22 people who have Upper respiratory tract infection and Systemic lupus erythematosus from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>
Systemic lupus erythematosus (an autoimmune disease, which means the body's immune system mistakenly, attacks healthy tissue) can be treated by Plaquenil, Prednisone, Hydroxychloroquine sulfate, Cellcept, Imuran (latest reports from 12,649 Systemic lupus erythematosus patients)
Upper respiratory tract infection has been reported by people with tendon rupture, fever, rashes, breathing difficulty, diarrhea (latest reports from 15,354 Upper respiratory tract infection patients).
On Jul, 26, 2016
22 people who have Systemic Lupus Erythematosus and Upper Respiratory Tract Infection are studied.
* Approximation only. Some reports may have incomplete information.
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.
Hi i am Maddy and i am currently having tests for lupus. I was an incredibly fit person up to around 18 months ago. I had slightly raised blood pressure and was out on ramipril. I also got the flu and after that i have had recurring pleurisy symptoms accompanied by the most incredible fatigue i cant eat properly and i have lost a lot of weight. I also get sweats and chills and i did fet a butterfly rash one day when i went out in the sun but i thought it was the antibiotics i was on at the time. I suffer breathlessness and my shoulder muscles seize up. I am off the ramipril as i ran out and my blood pressure was okay so with the doctors consent i chose to stay off it. i've been off it a few weeks now but i am just recovering from a really bad bout of symptoms. I have paid to see consultants three times to try to get a diagnosis hence the blood tests relating to lupus. Does this all sound familiar to other ramipril users? Will my symptons eventually go?
I'm really just looking to find people who have taken aldara and have lupus. I want to know someone somewhere has successfully completed a treatment without any huge issues. I've had a rx sitting here for a month, but Im affraid it'll cause a flair.
Hi i am Maddy and i am currently having tests for lupus. I was an incredibly fit person up to around 18 months ago. I had slightly raised blood pressure and was out on ramipril. I also got the flu and after that i have had recurring pleurisy symptoms accompanied by the most incredible fatigue i ...
I was diagnosed with lupus in 2002. Around the same time my doctor put me on losartan potassium. Also around the same time I began having a skin rash. I recently came across research that losartan can cause subcutaneous lupus. I have suffered from this skin rash for all these years. I am ...
Hi there, Just joining the group. I've had SLE for 28 years. This is the first time I have experienced Cellulitis. It started in my knee when I was on vacation. The ER Dr. gave me a script for Bactrim & Prednisone. The knee is looking better but I feel terrible! I am itchy all over. Has anybody ...
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.