Lupus is reported only by a few people who take Sulfamethoxazole And Trimethoprim. We study 6,243 people who have side effects while taking Sulfamethoxazole and trimethoprim from FDA and social media. Among them, 4 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 preventive health care. (latest outcomes from Sulfamethoxazole and trimethoprim 6,906 users)
Lupus (any of various ulcerous skin diseases) has been reported by people with breathing difficulty, fever, rashes, drug ineffective, systemic lupus erythematosus (latest reports from 22,170 Lupus patients).
On Sep, 17, 2016
6,243 people reported to have side effects when taking Sulfamethoxazole And Trimethoprim.
Among them, 4 people (0.06%) 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'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.
It took the doctors years to diagnose me with lupus. I have always had low platelets. *Cannot take aspirin; or anti-inflammatories: I take pain medications for bulging disks; migraines frequently; and have had (5)five infusions of IVIG. Now I will be trying this new drug, called "Promacta." ...
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?
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 ...
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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