There is no Rsd reported by people who take Botox yet. We study 2,148 people who have side effects while taking Botox from FDA and social media. Find out below who they are, when they have Rsd and more.
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 >>>
Botox has active ingredients of botulinum toxin type a. It is often used in migraine. (latest outcomes from Botox 26,273 users)
Rsd (reflex sympathetic dystrophy) has been reported by people with pain, osteoporosis, complex regional pain syndrome, depression, osteopenia (latest reports from 3,097 Rsd patients).
On Oct, 26, 2016
No report is found.
Hello. My name is Susan, I'm 64 and I have been using botox for 5 yrs or so for dystonia. I started when my larynx would spasm shut so I couldn't breath and my neck was pulled so far to the right I couldn't drive. I have always been a great sleeper but for the last few years have increasingly long and severe bouts of insomnia. I have been sleeping 12-15 hrs for a couple of weeks and it just dawned on me to question whether the botox is the cause. I am due again tomorrow. Almost any drug that says may cause drowsiness "wires" me including pain meds. I am going to be keeping track of it now but am really happy to find a site where others have reported the same. Thank you.
Hello. My name is Susan, I'm 64 and I have been using botox for 5 yrs or so for dystonia. I started when my larynx would spasm shut so I couldn't breath and my neck was pulled so far to the right I couldn't drive. I have always been a great sleeper but for the last few years have ...
Hello I've had RSD/CRPS ... from a car accident in Nov.7th, 2007. my left femoral nerve was damaged ... I now have in in my neck ,right foot/leg, and possibly on my right elbow from tendonitis ...I pray for a cure from this horrible disease..
Hi , When I was 55 , I developed RSD in my foot ( mostly toes ) after having Acl replaced knee surgery . I had an undiagnosed pheochromocytoma at the same time . . It was found incidentally when I had an abdominal scan 6 months after my knee surgery . My lab work showed a slightly elevated ...
Hi everyone, Thank you for letting me join your group. My name is Mary, (Mary1016), the major illnesses I suffer with is Complex Regional Pain Syndrome/RSD, small fiber peripheral neuropathy diagnosed with biopsy two weeks ago. I was told the neuropathy was already severe and the thing to do ...
This is the first time I've posted anything on any website about my journey. After a couple misdiagnoses I was diagnosed with RSD 8 years ago. Prior to being a patient I was a doctor. Talk about a rude of wakening! My symptoms were confusing. I knew I was very sick, but didn't know how sick. ...
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