Tardive dyskinesia is found among people who take Celexa, especially for people who are female, 60+ old , have been taking the drug for 2 - 5 years, also take medication Seroquel, and have Depression . We study 37,154 people who have side effects while taking Celexa from FDA and social media. Among them, 158 have Tardive dyskinesia. Find out below who they are, when they have Tardive dyskinesia and more.
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Celexa has active ingredients of citalopram hydrobromide. It is often used in depression. (latest outcomes from Celexa 40,733 users)
Tardive dyskinesia (a disorder that involves involuntary movements) has been reported by people with indigestion, abdominal distension, bipolar disorder, depression, schizophrenia (latest reports from 25,780 Tardive dyskinesia patients).
On Oct, 26, 2016
37,154 people reported to have side effects when taking Celexa.
Among them, 158 people (0.43%) have Tardive Dyskinesia
* 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.
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 now is get me to a neurologist that specializes in pain medicine. Couldn't get an appointment until November 4th and am having great difficulty waiting. I'm going for another ketamine treatment this Sunday October 2nd. I was told by Columbia University after a failed lidocaine infusion, to go back to the ketamine doctor even though it made me start peeing blood. I don't have a lot of information on sfn. I want to basically know how long somebody usually lives when the Polyneuropaypthy is severe already. When my doctor gave me the results he hugged me for a long few minutes and told me basically not to loose my faith in God and to promise I won't take my life. I made those promises but I need to know how much worse this can possibly get and how long do people usually have to suffer. Thank you for taking the time to read:-)
Hello, I am 21 years old and developed a form of td from being given metoclopramide while studying abroad in England. I was on it for two days and now my brain gets foggy all the time, I have unexplained pains and muscle spasms and I can't drive or work full time. I can't have sex without being in pain, because it makes my spasms worse. And I got off easy, from what I hear; and yet I can't bear this pain. I really want to end my life. I am so scared and angry and sad. I can't imagine living the rest of my life like this. I can't cope and I don't want to. I feel like a human who's been experimented on; They never warned me any of this could happen. I cannot believe that people cant prescribe a drug that can turn a person into this and they have no idea how to fix it. It is like living in hell and there is no escape. It should be a crime worthy of jail time. They murdered my life. I wish I had the balls to commit suicide so my pain would be over, but I don't really want to die. I want to live. I want my life that they stole from me; but I can't have it. So I wish I would get hit by a car or die of some natural cause. I seriously believe I would rather die than live a life of coping with this; no amount of coping will change the fact that my life from here on is suffering. I don't know what to do and don't think I can deal. I wish I were dead instead.
I've had RA for 26 years. I was on Methotrexate for 24 of those years. I've tried Xeljanz for a month. Made me weak, nauseous, major headaches etc. Tried Enbrel, results not good. Humira, results were no effect or side effects, can't afford. However it seems Zyrtec seems to help my allergies and ...
My daughter was recently prescribed celexa 30mg with trileptol 300mg twice daily for an attemped suicide she is 15, was diagnosed while in the mental health hospital with adolescent depression and anxiety.She has now been on this medicine for 2 weeks and is shaky and extremely lightheaded also ...
Hello, I am 21 years old and developed a form of td from being given metoclopramide while studying abroad in England. I was on it for two days and now my brain gets foggy all the time, I have unexplained pains and muscle spasms and I can't drive or work full time. I can't have sex without ...
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 ...
(59 yr male) I developed tar dive dyskinesia suddenly while taking Abilify and had to stop taking it. My dyskinesia disappeared fortunately. Now the Doc wants me to start Mirtazipine instead. But I've since read that dyskinesia is still a risk. I worry as dyskinesia can be permanent. Any ...
I just realized a couple of days ago that I have tar dive dyskinesia. I am a registered nurse and have monitored patients for this condition for years. It just dawned on me that I have TD. I have taken protonix for about 1 year.
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