Lupus is reported only by a few people who take Sulfamethoxazole And Trimethoprim. We study 6,436 people who have side effects while taking Sulfamethoxazole and trimethoprim from FDA and social media. Among them, 5 have Lupus. Find out below who they are, when they have Lupus and more.
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Sulfamethoxazole and trimethoprim has active ingredients of sulfamethoxazole; trimethoprim. It is often used in urinary tract infection. (latest outcomes from Sulfamethoxazole and trimethoprim 7,114 users)
Lupus (any of various ulcerous skin diseases) has been reported by people with rheumatoid arthritis, systemic lupus erythematosus, crohn's disease, multiple sclerosis, osteoporosis (latest reports from 23,212 Lupus patients).
On Oct, 19, 2016
6,436 people reported to have side effects when taking Sulfamethoxazole And Trimethoprim.
Among them, 5 people (0.08%) have Lupus
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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.
I have shortness of breath, a bad cough, loss of taste, slight numbness all over, dizziness, light headedness, a rash on my stomach, and fatigue. I have been taking the medication for 4 1/2. The pharmacist instructed me to stop taking it and sold me an allergy medication to treat symptoms. Hoping my sense of taste will come back and there isn't extensive damage to my lungs, as I've read shortness of breath can indicate that.
I am 27 year old male. I have SLE. I get a lot of discomfort and pain in my chest and upper back. It migrates throughout the day and changes in quality. It can be overwhelming. Sometimes I have a hard time breathing, sometimes my heart races. Sometimes my face gets hot and sweaty. I thought it ...
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.
Hello my name is Carolyn Martin. My daughter Shannon got Lupus when she was 17. She lived another 13 years before dying at the age of 30. She has 2 children both boys that has no mother now. She was on accutane at the age of 14 for acne. I am pretty sure that is what gave her lupus. She got ...
Hi my name is Lisa I am Dx with Lupus this year , so I am a newbie. I sometimes have aches and pains, but I take my anti inflammatory medicine . I won't give up on life . This I illness will not hinder me from my job and enjoying life as well.
I have Lupus Nephritis and my flat warts are taking over my body. For years I just had one on my leg and then it starting spreading up the leg. I have had them burned off many times with zero success. Now they have traveled to both arms and my back. Any suggestions on how to get rid of them ...
I've had lupus for 10 years. On plaquenil for ten years. Now having to withdraw from plaquenil due to a myopathy caused by it. Having a terrible time with nausea dizziness and joint pain fatigue. Anyone else come off plaquenil. What was your experience?
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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