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Found 55 results

  1. street129: hi

    just need to understand the taper, im on 250mg of trazodone, started tapering on my own cause i had no where to turn and noone to guide, since i was directed to this board can you please so that i can be sure to do this right, i strated doing 200mg, as i read the board i see its wrong, i have been doing 200mg from tuesday to thursday when i saw this board friday i started doing 225mg for the 10 percent, i had stop 1 day before i reinstated and began tapering, no one told me i was gonning get addictive, i was shaking and itching when i had stop, im still itching and not feeling myself. anyway saturday i did 225mg and tonight i will do 225mg, am i on the right track, thanks in advance.
  2. Hello all, New to the site. A little about my situation, After being prescribed 300mg gabapentin twice a day + 900mg before bed, 15mg remeron before bed, and 100mg trazodone before bed for what's said to be anxiety disorder that appeared out of no where. I visited a psychiatrist per the hospital. It took me two weeks to find one to see me, upon my visit she says that she wanted to get me off as much as possible as she thought the gabapentin should be all I needed. She stated that I should be able to stop the Trazodone and remeron right away with no issues. I questioned weather this was a good idea.... Anyways I decided that the trazodone had to go first because of the side effects I was having from it tapered from 100mg to 75 for two days then fifty for two days noticed a slight down feeling then 25 for 4 days "what a mistake" on the forth day I felt so bad racing thoughts of hurting myself, really bad depression "which I have never had" and more than an hour of servere anxiety if not for the gabapentin surely I would have been flailing around like a fish out of water. I found this site that night after everything seem to calm down and decided to updose. I owned a mg scale and went back up to 37.5mg. First day was great present day not so good, pretty ok morning around 12pm started having stomach issues and some feeling down laid on the couch for several hours started to feel better so I went to the gym and did my daily 8 mile bike ride. My problem is that I am supposed to return to work on the 30th or lose my job and insurance.I don't know if I updosed correctly or how to stabilize enough to return to work. I would appreciate any advice I can get at this point. So upset because this is the first time in my life I have had to take any meds daily, feeling so lost.
  3. Hello, New member here. Had been on Klonopin for 15 months for insomnia caused by hypothyroidism. Been off K for 10 months now, with the help of 75 mg Trazodone for sleep. About 2 months ago, T was losing its effectiveness and I decided it's time for a drug-free me. I went from 75 mg to 50 with no problems; at 50, withdrawal hit hard. Insomnia (of course), shakiness, anxiety, you name it. I did a fast taper as I did not have it in me to go through another long taper after the K experience. In 2 months, I went from 75, down by 1mg every night to 50, to 25 for 2 weeks, 12.5 for another 2 and finally off. I have been off for only about 3 nights. Withdrawal after quitting seems manageable so far, although it is too early to tell if it will get worse. My main issue is with insomnia. I feel if I can manage this, I will be OK, especially after the horrific K withdrawal. My question for those who have used Trazodone: how long did it take for sleep to return after quitting trazodone? Please include how long you had been using T and the dosage. Thanks for your input and hope we all survive the trials of psychotropic drugs. Survivor1
  4. Hi fellow members. I took Trazodone and Cymbalta for over a decade. These drugs were prescribed by my family doctor for neuro-muscular pain and related difficulty sleeping. (The real cause of the pain was ruptured discs in my back but I didn't learn that until I'd been on these drugs for years.) I've tried to get off of both drugs several times but all doctors did in the past was give me the next lower dose of each drug, which didn't work, and just drove me right back to my previous regular dosages. Well, thanks to tappering info I learned from this discussion group, I've been off both for about a month. The problem is that my withdrawal symptoms are seemingly getting worse. so, I could use some coping advice. The biggest problem is dizziness, or I should say passing out in my case. The week I finished the taper for both drugs (about a month ago) I passed out and gave myself a mild concussion when my head hit the floor. I was in a classroom setting so they sent me to the emergency room in an ambulance. They ran lots of tests at the hospital, all of which all came back normal. I thought the fainting was a one-time occurrence. Yesterday, I passed out again and hit my head, again. I was at home so my husband didn't take me to the hospital as the lump on my head wasn't too bad. Other symptoms of withdrawal I'm having include irritability, anger, depression and even suicidal thoughts. I've never had a problem with any of those things before so I'm naturally frightened. I've tried medical marijuana for these symptoms but have figured out (I think) that they were making my sudden drops in blood pressure, aka dizziness, worse. Does that make sense to anyone? I still haven't found a doctor who would/could help me with these symptoms. At this point I don't know if I should keep looking or not. I live in rural Arizona so expert doctors, if they existed on this topic, aren't plentyful. Today I looked at The Road Back Program's anti-depressant withdrawal supplements and found a link to this discussion group's moderator who said not to waist money on them. It felt really good to get objective advice from the moderator. I just need more practical advice, especially about the sudden drops in blood pressure. I'm feeling afraid to drive my car. Is there something I can do to better manage the dizziness. Can these symptoms really last years?!
  5. Cheers, everyone First – english is not my native language, so forgive me, if it's a bit clumsy. Second – this story may be long. I feel like sharing, yet I'll try to make it short. Everything began 11 years ago, when – after a great deal of trauma – I was diagnosed with obssesive compulsion disorder. Diagnosis itself felt wright – my fears, obssesions and rituals were getting stronger every day. Soon, I was beginning to lost it. Psychiatrist prescripted SSRI meds – sertraline, to be specific. It was pain. I reached the dose of 120 mg a day, as she ordered – I wasn't sleeping whole nights, wasn't eating almost anything (but still got fat) and my feelings and emotions were lost completely – what was left of me was a complete cyborg. Inabillity to sleep and eat made me going mad, my shrink, however, didn't see any problem. After a half a year, I showed her my middle finger and cease the treatment. I felt great for about a year – then obssesion came back, stronger than ever. This time, a proffesor psychiatrist came with paroxetine. Let me make this clear – paroxetine did help me. My obssesions were gone. I became calm, reasonable, able to deal with emotions like grief or anger quickly. In time, however, I grew more and more disturbed about the therapy. I mean – what about my personality? Which part of that is artificial? What kind of person would I be without drugs? Why other people mostly seem a bother to me and why I lost any kind of interest in any kind of love life? Why I'm getting more and more surly and bitter? My proffesor answers were another drugs only, to which I refused. This year, when six years of paroxetine were coming to pass, I withdraw it. I thought reducing the dose slowly will do. At first, I felt better. Everything was so vivid, so lively; I was becoming nicer to people. All this didin't last long, though. At first, I became nervous. Everything started to seem difficult, I felt like I had to much to attend to. That deepend into depression so deep, I quickly started to think about suicide, which eventually made me to come back to my treatment. This time, side effects decided to say hi. Afer two days on one pill, I suddenly started to run around house in cricle with suicide thoughts so intense, it was like someone grabbed me, shaking my arms and screaming „Do it! Do it! Do it!” I almost tried. I made it through next few days on benzodiazepine. Then, paroxetine kicked in without any more events. I've put myself together, yet I was confused – I mean, what the hell happened? I've never had such depression, where did it come from? My main problem were obssesions. I started to wonder – what if paroxetine actually did all this and now I'm allowing fox to guard henhouse? My decision to have a closer look on this brought me to book „Deadly Medicine and Organised Denial” by prof. Peter Gøtzsche (to those who haven't read it already – it's a book everyone should read). I read that paroxetine – and other SSRI meds – actually cause depression which shows up in the withdrawal syndrome due to disrupting brain biochemistry and that withdrawing after more than few weeks of treatment can be very hard. Sudden suicide thoughts, according to this book, are quite popular side effects of paroxetine syndrome. So many people, I was thinking. So many people did commit suicide, many of them slaughtered their families first. I was furious and quite dispaired, feeling like I'm gonna claw my doctor's eyes out. Who the hell allowed this **** to be on market? Why my god damn shrink is keeping my on this crap for years? I've felt like a freaking junkie. On the other hand though – after I calmed down – I've felt some kind of new strenght. Withdrawing became my top priority. I'm now aware what happened and what is next. I know it may be hard, but I'm not losing optimism, until I still have at least some part of my brain intact (and liver, and kidneys, et cetera...). Like I said, I got this site address from prof. Gøtzsche and here I am. On the next appointment, I'm gonna have a little chit-chat with my doctor. If he won't be willing to assist me on my way to withdrawal, I'll find a doctor who will. I've already reduced the dose from 40 to 30 mg and I'm aiming to reduce it more to 20 mg (this is by approval from my current doctor). And then... well. No matter how much time will it take, I'm gonna be free one day. (Anyone who thinks deserves beer after reading all this, leave me a note ).
  6. I wanted to share my story, hopefully I can find someone that can identify themselves with my ordeal and possibly help each other. I still can't believe I'm typing this out, its all very surreal to me, I never in my life would have imagined that, at age of 21, I'd be tossed into this mess. Not only dealing with anxiety but now terrible thoughts of suicide ever since getting PSSD. I was given Trazodone 50mg after having problems sleeping on July, I told my doctor I had some issues sleeping, she then proceeded to ask some mental health questions and I told her I had minimal anxiety and that whether I had depression was debatable.I only took the pills 3 times, I stopped after realizing I could barely get an erection. Then came the initial crash, there was pain in my testicles that felt like blue balls, the veins in my testicles got inflamed and painful especially when I got an erection. I ended up jerking off, I thought it would alleviate the pain and go away, the semen was unusual, I never came so much in my life but the consistency was watery. I also suffered from terrible abdominal and pelvic pain which has gone at least 90% away in the two months that followed, it was annoying and really hard to concentrate on my studies but I thank God that’s gotten better. I'm not sure how common this is but I feel like my left ******** shrunk, I wonder if anyone on trazodone or other anti-depressants has had shrinkage of only one of their testicles. I also have Urinary incontincancy.It got to a point where I had to tell my parents, it was embarrassing, I cried and told them these pills changed me and that I'm not ok. I was pretty much saying my goodbyes, it's so easy to just end the pain and kill myself but after a long discussion I'm going to wait this out as long as I possibly can. I can't just do this to them, they’ve suffered so much and given me more than I could ever ask for, I can't end my life knowing I'd leave them in so much emotional suffering.I posted my story on another forum as well. Could this be PSSD, chemical epididimytis, prostatitis, pelvic floor dysfunciton? The symptoms with many of these conditions seem to over lap, What I do know is these problems are directly due to Trazodone. I'm just not sure where to go with this problem now, I honestly can't see myself living a whole year with this.
  7. I took trazodone contramid 150 mg for 1 year, for one month I take 75 mg. In the past I took entact for 8 years (for anxiety and panic attacks), then a year out, after for 2 years cymbalta. Because I have sexual dysfunctions since 2015 I switch to trazodone one year ago that did not solve my problems, I have the symptoms of Pssd! I need to take off this drug for my dysfunctions, but I'm anxious, I can't take off this drug!
  8. Greetings all, Around July of last year i suffered a direct blow to the temple (by far the worst pain I've ever felt in my life) which lead to me having a concussion, shortly after that I smoked what I thought was weed with my roommates but it turned out to be a drug called Spice. These two events led to me having hallucinations one day and I checked myself into a hospital. Long story short they didnt diagnose me with anything they just doped me up with 8 different medications some of the ones i can remember are Abilify, Depakote, Risperdone, Zyprexa, Ativan, Vistril, and Lithium ( i can't recall the other drugs names). I was on so many meds I don't remember the first two days I was there. Long story short they held me against my will for three and a half weeks before I was able to get a different doctor and get released. Since my release I have felt emotionally numb i cant feel happiness or joy, sadness nor pleasure. I feel like I have lost some intelligence, as well as vocabulary and my creative ability. Prior to being given I was very creative all my life I enjoyed writing music and poetry, I also loved playing sports mainly football, Working out, Playing video games and watching movies. I no longer get any enjoyment what so ever from anything i once found interesting. I find it hard to carry on a conversation I feel socially unconfident due to the fact that I feel like i cant think like my brain is just an empty slate. I get major headaches that occur pretty much everyday, I have insomnia (I can fall asleep just fine but wake up at the same time every night which is 3 am). Also I have experienced a tremendous loss of libdo and interest in sex like i just dont desire it anymore, I really feel like I lost myself and I'm scared that I wont get my pre-med self back, I have been doing everything in my power to get my life and old self back I have been seeing a pdoc who prescribed me zoloft which I feel isnt working and also trazodone to help with sleep. I have also been going to counseling sessions weekly which has helped a little. I have done extensive research and have come across many people who are experiencing the same things that I am and we all have the same question can the brain recover from antipsychotics and if so how long does it take??
  9. suzibelle: Trazodone

    I successfully tapered off benzos 20 months ago but have been very ill since my last dose. I thought is was protracted withdrawal but I an now suspecting it is the Trazodone making me feel so bad. I have been taking it for 7 years and I'm wondering if this drug made anyone else feel really horrible?
  10. Aria's recovery from poly drugs. I had no idea when I walked into a psychiatrist's office 25 yrs ago the horrible labyrinth I'd entered. Slam dunked at a point in my life when I was feeling low and the loss of future possibilities taken away. Being told I was mentally ill, would never function again, needed to be on disability and poly drugged for the rest of my life repeatedly took it's toll. All this impacted my relationships with family, friends and enjoying life. The pdoc constantly added new psych drugs, changed doses and took me off the old drugs at an alarming rate. I became a morbidly obese woman who mumbled or talked rapidly and it was obvious to everyone but the pdoc I was totally messed up on something. I had Seroquel Induced Acute Pancreatitis that landed me in the hospital for quite awhile and my pdoc put in my open med chart I was crazy. I didn't know this till later but ill as I was I did notice some of my physicians were treating me oddly. One good thing about being so ill was I referred to a neurologist for chronic pain and found out my problem was profound drug induced Akathsia. This neurologist actually screamed at me, these psych drugs are killing you, they're killing you. I knew I had to get off these drugs not matter what it took and reclaim my life. At my next appointment I asked my psychiatrist why he was drugging me like this and he looked directly at me (probably for the first time in years he saw "me"). He started sobbing, loudly sobbing, "Oh God what have I done to you", over and over. I'm sitting there thinking oh crap, I don't need this. Our 15 minute med check was up and this guy calmly goes to the front desk to get the next patient and proceeds without any other fanfare. He's robot. A robot. All this in itself was mind boggling. Hell, closure?? No way. I found out I had Tardive Dyskinesia and a few other psych drug induced issues. My face was a road map with twitches and jerking that yelled hey, I'm on massive psychiatric drugs. Will my face be like this forever?? The TD has mostly gone away and I'm so grateful (the pdoc adamantly said I did not have Tardive Dyskinesia from psych drugs). Well, guess what?? The psychiatrist was wrong...horribly wrong. Other doctors, psychiatrist, therapists said you're not mentally ill and never had been. The sad but very scarey part is I'm labeled as profoundly mentally ill and that info is in my medical charts. One pdoc did this...one. I've gone through the gambit of emotions dealing with this. I will probably always be mad at this jerk for what he did to me and for what he still does to others. It affected years of my life and he was wrong. I'm a Success Story because I'm psych drug free and have been for several years. My journey was extremely difficult and I did it on my own hit or miss tapering off numerous psychiatric drugs. I endured drug withdrawals that paralyzed me month after month. Was it worth the hell of tapering? Yes, very much yes. My reward was my clarity of mind, my passions for life returned and I have hopes for my future. I mended fences with family and have made new friends. I strive everyday to be productive. I'm me but a different me because no one could go through all this and not be changed by it. (for more in-depth conversations about my struggles, coping and self awareness with surviving psychiatry please visit my ongoing thread Aria's Psych Journey http://survivinganti...psych-journey/)
  11. Hello everyone! I joined this forum because I'm in trouble. I really am. My life took a turn for the worse and I'm stuck into a real nightmare that keeps torturing me in the same fashion, every day. I started taking psychodrugs in order to deal with a strange insomnia that actually hit me out of the blue. The only apparent cause I was able to find was a recent antibiotic therapy with a drug (Levofloxacin) known to cause symptoms of anxiety and mental hyper arousal in predisposed people and mimicking benzo withdrawal. Such an unexpected side effect would have taken a toll on me if it hadn't been for sedative drugs, so that's why I started taking them. I am relying on them to lead a somewhat normal life. Or something that resembles one. Just pointing this out, I never had any mental issues before. I was prescribed a benzo to deal with insomnia and was on Klonopin for six months. I successfully withdrew from it with a slow taper, since it became ineffective in just a couple of weeks... I have been on 80 mg of Trazodone for about one year and 17.75 of Quetiapine for five months now. I'm on the combination of both now since Trazodone alone wasn't providing me more than 3 hours of sleep. And Quetiapine alone causes me a helpless depression... If I take them together at nighttime I actually can sleep for 7 solid hours. However, something is definitely wrong with these drugs. I'm scared of what they are doing to my brain and my body. I have chronic strange vibrating feelings all over my body, but mostly in my legs. They ache, all day long. My body feels hot and I'm very heat intolerant. My joint aches a lot, especially my ankles, and when I use them a lot my wrists. My feet tingle, burn, sometimes are numb and I have mild pin and needles sensations. Not to mention the strange vibrating feelings in my mouth, in the gums, like someone is trying to electrocute me! I get them with no apparent reason, and prevent me from relaxing spontaneously. Like I was always on an adrenaline rush. And, of course, taking the drugs is the only thing that stops them... I can't relax on my own, I always need a chemical help. It's virtually impossible to stop these vibrating feelings if I don't take the meds. I'm almost comatose in the morning, I just can't think straight and it takes me hours to be able to 'think' and reason again. I sleep well but I always have very vivid dreams when the drugs are wearing off. It's hard to tell if I'm awake or just dreaming, it feels like I'm thinking at an unnatural speed. I have no control over my thoughts, anyway. In addition, I always been very smart and with Quetiapine I just feel retarded. I can't think it straight. Then, all of a sudden, in the late afternoon, I feel like someone came to unchain my mind, and I start thinking so fast i can't focus on anything, I feel like thins are moving too quickly and my body aches even more. I've always been taking the drugs at the tiniest effective dose and I don't want to take more during the day. I start easily, I can feel a rush of electricity in my body at every sound and I just can't calm down. It's not even anxiety. I never got a panic attack. Sounds more like hyperactivity and restlessness! I've tried to withdraw from Trazodone but taking less than 50 mg caused me to burst into tears and feel absolutely hopeless. I'm on a paleo diet right now, high in berries, fresh fruit and organic lean meat, I take zinc, magnesium, potassium, as well as probiotics and colostrum since I have been diagnosed with a bad form of leaky gut and chronic body inflammation, but they proved to be unable to prevent these relapses and these odd pains. Is really such a tiny dose of Quetiapine causing this? It shouldn't even affect my dopamine receptors at that dose, should it? Are my issues caused by noradrenaline instead? I'm I'm only 25, I don't want to spend the rest of my life on drugs that are doing more harm than good.
  12. I would appreciate assistance on tapering. My daughter is taking Zoloft 200 mg, Topiramate 25 mg (mood stabilizer), and Trazadone 50 mg (sleep aid). I have done extensive research trying to find which medication to start the tapering 10% method first, second and then third. I've not discovered any information on which one to start with and the sequence order. Would I start with the Zoloft first, the Topiramate second, and then Trazadone last? Or should I have her start with Topiramate first? What are your thoughts of tapering the Zoloft to 100 mg and then starting the Topiramate taper? Thank you in advance for your assistance.
  13. I'm 45 years old. I have been on psychiatric drugs since I was 25. For years, 17, I was on Paxil 20mg and tegretol 200mg. I believed I tripped off my first depression after using ecstasy, which I think altered my brain's serotonin functioning. Four years ago I went to my gynecologist seeking help for worsening pms, as I believed perimenopause was coming into play. I failed to consult with my psychiatrist and trusted her. After a too-quick taper off of Paxil and onto Lexapro things just completely deteriorated. After 6 months I was a wreck, did another, even shorter, taper off of Lexapro back onto Paxil. But I was sunk...I think my central nervous system was wrecked. The ensuing year of onto and off of a variety of drugs was nothing short of a nightmare. Sparing all the details, I landed on the following drugs: Remeron 15mg Paxil 20mg Lamictal 125mg Pristiq 100mg Lithium 600mg Klonopin .5mg Trazodone 50mg It's criminal. A John's Hopkins psychiatrist specializing in women's hormone related mood issues said my gynecologist's cavalier actions verged on malpractice. A recent, and current, rash believe to be pityriasis rosea prompted my current psychiatrist to insist I stop Lamictal cold turkey. The dermatologist diagnosed it. He, without seeing the rash himself, is insistent. In light of what I feel is a damaged central nervous system I have decided to trust my dermatologist. That said, this situation has prompted me to consider the idea of eliminating the Lamictal. It's a start. I also believe Lamictal in some way tinkers with estrogen, something I'd like to avoid. It has been a hellish journey. I do not trust the psychiatric industry. I believe that how my case has been handled, so carelessly and without regard to actual true health, is shameful. I never, ever thought I'd be on multiple drugs like this. I am a high functioning, intelligent woman with a constitution sensitive to endocrine changes. I have been terrified of even considering touching any of this. While in the back of my mind wondering....what will happen to me after years of being on so many drugs? For the record, I have never been manic, ever. Lithium does function for me as an antidepressant. I understand that I'm somewhere on the spectrum, and because of long periods of happiness and wellbeing interrupted by 3 episodes of major depression, each with clear origins, I have been labeled bipolar2. I don't care much for labels. All I know is I'm on a serious amount of drugs. And I'm finally willing to find the courage to wrap up this bizarre ride. Lamictal first. Thanks for reading. Any encouragement or feedback gladly welcomed. Hope
  14. in 2014 I got off all SSRI's after being on them intermittently for 20 years. I was probably on them half of the time. In 2013 I went on Trazodone for 3 years for insomnia. Started on 200mg and went down to 100 over the first year. I did not take it daily as my doc said it was not an SSRI so I should take it as needed. I would take it 4-5 nights a week and take Sominex on weekends. I tried to taper down to 75mg but couldn't function at work the next day so I held at 100mg. In Mid June I took a month off from work and decided to bite the metaphorical bullet and stop Trazodone cold turkey. I know it was a bad idea, but I needed a med free month to establish a sleep pattern. It worked but I'm paying for it as I knew I would. Dealing with weird pains in my chest and back, mostly esophageal pain. My personality has definitely changed, but it changed before I got off Trazodone which is one of the reasons I got off, just seems worse now. The other expected side effects showed up, depression, anxiety, suicidal ideation. I'm able to handle all of these because I am FINALLY sleeping med free for the first time in years, I was just wondering if anyone else had gone cold turkey from 100mg and how long until I start feeling like myself again. Thanks in advance. And yes I know cold turkey was a bad idea but under the circumstances it was the best choice.
  15. Hi I'm on fluoxetine 40 mg for the last 6.5 months. and my psychiatrist prescribed me trazadone for sleep. I was taking 12.5 mg a night occasionally 25 mg for nearly 5 weeks. She told me that it wasn't addictive and could stop it when I wanted. Well I did and two days later I broke out in hives and itching then over an 8 day span anxiety and depression built. Which is where I am now. Can I reinstate the trazadone at 12.5 and stabilize? She also wants me to start abilify 2 mg
  16. Having successfully weaned from gabapentin, I felt ready to begin tapering from duloxetine. Then I found this site, entered my meds & viewed the interaction between them and I feel rather worried and would like help knowing which to leave off first. The ones I'm concerned about are duloxetine, amitriptyline, and trazodone. I also take tizanidine. tia
  17. Hi everyone. I've been on several psych meds since December 2015. I was diagnosed with bipolar disorder and PTSD. I am on gabapentin, wellbutrin, trazodone and lamictal. Over the past few months I have noticed increased side affects: dizziness, losing my balance, involuntary movement, and severe gastrointestinal issues. I talked to my psychiatrist about getting me off the medications and she is not supportive. She said I need to be on them for life, like a person who has a physical disease. I got sober a year ago from alcohol, am active in my church and recovery community, eat healthy, exercise, and feel I can handle life without being medicated at all. I'm starting with the gabapentin (10% taper) I'm already having anxiety and side affects. I know I have to go slow, one medication at a time. This is really scary and I'm worried I'm never going to be off all of it. I'd appreciate any suggestions.
  18. I've been taking these meds for years. I've been on them mostly for extreme anxiety and depression. What do I need to help with anxiety and depression as I try to get off of them so I can stay off of them. Also, how bad is getting off of fluoxetine, trazodone, wellbutrin compared to getting off of Effexor? Getting off of Effexor was pretty hellish.
  19. Hi all, I am new here but I've been reading posts since last fall, when I started weaning off the Gabapentin I was put on a month before, pre-herniated disc surgery. Surgery went very well, stopping Gabapentin was a horrific nightmare of about 5 months. However, the results were so amazing I felt encouraged to get off Effexor as well. I was put on Effexor for fibro, stopped cold turkey when I got pregnant (wowza!), then was put back after postpartum depression. Six years later, here I am. So now comes the question: My recommended taper for Effexor XR 75 is Effexor ER 35 (morning) + Trazodone 50 (evening) for a week, then half the Effexor for a week, then stop the Effexor. (Whatever I do with Trazodone afterward is left as an exercise to the taker...). I haven't found any information about this particular combination, and after the Gabapentin saga I consider myself an expert googler I can see that Trazodone itself is highly questionable, although the doses that I did take proved to me that I hadn't had deep sleep in years ( and that despite the daytime grogginess). Can the good people of this forum provide some insight into this combo? In particular, are the two medications in any way equivalent in effects, or am I going in withdrawal overnight and starting again in the morning? Taking the trazodone before the Effexor ER is completely out of the system lessens the "brain shut-down" effect, so maybe? My previous effects going cold turkey off Effexor were severe nausea, vertigo and horrifying "other" gasto-intestinal symptoms . After Gabapentin, which had shocking vertigo plus a whole host of other physical and mental symptoms (like bouts of extreme rage), this doesn't seem too bad, which is why I agreed to a fast taper. Internet suggestions I have found helpful up to this point to mitigate symptoms: Omega-3 in large quantities, protein snacks (edamame and toasted pumpkin seeds worked particularly well), ginger and liberal curry-like spice combos in the food, sun and sweat-inducing exercise (my garden has never been so weeded and trimmed).
  20. Hello everyone new to the forums here. Just wanted to start off by asking a question that I hope someone with experience or knowledge about the topic could share information here. I've been searching all over the Internet and every trazodone story is either about withdrawal symptoms or how it helps people, or how it's not helping anymore.. I wanted to ask a different question which is: AFTER withdrawals and a proper successful discontinuation, what is life like? Is it improved or worse due to less sleep? More energy throughout the day? Less foggy/groggy/slow mornings? Don't need 2 cups of coffee to wake up? Do you have more motivation now that you aren't on a drug with tranquilizing-like effects? Less brain fog, faster response time etc? Or what in your experience is it actually like? It's very possible all those side effects I listed are unrelated to my trazodone usage but I genuinely think a lot of them are. (Not to mention physical sides) I'm also taking Wellbutrin for about same amount of time as I've been on traz. Vyvanse/Ritalin for add. My trazodone dosage is prescribed 150mg trapezoid shaped pills but I only take 50mg/night. Anyways I've been considering quitting trazodone to see if it helps. Basically all my side effects feel as though my add meds no longer help me like they used to. Do I just have a high tolerance to the add meds or is it possible the trazodone is holding me back? Trazodone has been such a weird drug for me that in the 7ish years I been on it I've never needed more than 50mg to get a solid 6-7 hours sleep. 8-12 depending on the situation but usually need 75-100mg for that amount of rest. That being said I only take 50mg that exact amount each night. I'm just curious if tapering off trazodone would improve my symptoms. If anyone has gone through this or similar please share your story I'd love to hear it. At 25 and half at 195 pounds 6 ft tall, I consider myself in good physical condition and my depression is MUCH better than it has been in the past. Anxiety is basically nonexistent (unless extremely stressful life situation occurs). But even then the anxiety goes away and is strictly situation related. ADHD is the only thing that really affects my daily life. I have impulsive add - interrupt people while they talk unintentionally, distracted easily, forgetful, lose concentration easily etc. all much much improved when I take my vyvanse (70mg) and booster Ritalin 10mg in afternoons. Though the effectiveness isn't what it used to be after being on 70mg vyvanse for 3 years straight no dose increases. Overall I wanted to hear your thoughts and if tapering trazodone might benefit me, or if my symptoms sound unrelated altogether. My goal is to get off the meds one by one taking it one step at a time starting with the trazodone, then Ritalin. Probably stay with vyvanse for a while as well as Wellbutrin (though I would like off that too in the future). Might try just tapering to 150mg wb and staying there a year or 2 and see how it goes. Anyways sorry for the long post hope it helped give a good intro to my story. Interested to hear a success story from abandoning trazodone and what life is like after completely tapering off. Especially interested in hearing from long term traz users, 2-10 years or more. Thanks
  21. Hi, I've been on and off every antidepressant for the last 22 years . I started antidepressants when I was 13 because my parents are pill freaks and I was being bullied in school and not happy about it. I've taken every antidepressant ever made and gone off most of them very rapidly. Over the years my insomnia, anxiety, and depression have gotten so severe I can't even function or see straight. I have trouble focusing my eyes. The fatigue is overwhelming and I only sleep 3 to 5 hours total a night. I took a break from meds for the last 1 year and 3 months from all meds and none of my problems got better. I tried Celexa for a week last week hoping it would fix all my problems but it made me much worse in every way however it did fix my vision problems and issues with a runny nose. I live in Los Angeles. Does anyone know where I can turn locally to fix my problems? What is going on with me? I can't live like this anymore. Pleas help!
  22. I am on Fetzima80 mg, Geodon 160 mg, Depacote 1000mg, Desaryl 600 mugs Klonapin4mg, Neurontin 1000 mg, Clonadine 25 mg, Percocet2 tabs/day and Tinzanadine 3 tabs/day plus meds forthyroid and Rheumatoid Arthritis. I feel like the meds are a major food group and I'm sick of taking so many meds I have been on this regiment for10 years. I need help on Howard whatto taper off first?
  23. Hello Survivors, I am wondering if you could help me shed some light on my symptoms. I would really appreciate any thoughts on my condition as the doctors have not been able to figure it out. I have had a spinal tap ruling out M.S. and 2 mri's of the head and neck, standard blood tests are normal. 9 months ago I had a series of stroke like episodes, intense fatigue and dizziness/vertigo and I ended up in emergency at least half a dozen times. It developed in to persistent dizziness and disequilibrium now going on strong for 9 months. A few months before this happened I was tapering off 15-30 mg of remeron and I also was taking ativan occassionally, perhaps 3-4 times per month on average. I have had severe chronic insomnia all of my adult life (I am 44 years old) and I found that 15mg of remeron was no longer helping me sleep like it did in the past so I stopped taking it or took it intermitently. I figure I ended up sleeping on average 4 hours per night, many times not sleeping at all for days even. But when I had the ativan I was able to get a descent night sleep, which was about once per week. Then the doctor decided not to take away the ativan and I was not getting that one good night per week anymore which I think was keeping me afloat. Most of my adult life I have had chronic insomnia so I am not sure if these new neurological symptoms are related. I started noticing that things did not look or seem right, or there was some spatial distortion and I had a general feeling of malaise leading up the weeks before I would experience the more intense dizziness/fatigue/stroke-like episodes. I also started experiencing tingling in my legs and feet, electric shock like sensations in my head (mostly at night), severe hypoglycemia, muscle contractions, tachycardia, swinging blood pressure (now it's mostly low), intense fatigue and weakness that sometimes felt difficult to breathe, feelings of travelling pressure in my head that sometimes would travel downwards in my body, a pressure in my torso like it was being crushed, heaviness in my legs, feeling like I am on an elevator or a boat, and other sensory distortions like having difficulty locating my feet in space. What made me concerned that it was MS was that my left foot felt like it had less feeling than the right at times I would wake up unable to move it for a few minutes - (it did not have the feeling of loss of blood sensation) but the foot feelings have passed. My doctor prescribed trazadone to help with sleep which has helped initially but I'm up to 150mg and often it doesn't work. When I add remeron it helps a little, but sometimes they both don't work for sleep. So I dont' take them consistently and at there has been days I haven't taken them at all because it seems the drugs don't really work anyway. 9 months later, mostly I am dizzy, like my brain can't catch up with my body movements or my balance and there is a light spinning sensation in my head, but sometimes my balance really gets bad. I have been offered Effexor, but in the past it made me more of an insomniac and I really would rather get off the anti-depressants as I feel like they might be the problem... Even though I feel like I am living in a nightmare I would rather ride out this neurological melt-down and try to heal naturally. Do my symptoms sound like it could anti-depressant withdrawal symptoms at all? And if so, is it possible to have permanent damage? I am concerned as this has no sign of letting up after 9 months. I am still as dizzy as ever. I have been taking remeron for about 7 years. Thanks for reading!
  24. I'm 32, I have a 6 year old, and I've decided I want to have another child finally. My GYN says, when you find out you're pregnant, just quit taking your medications. Wtf? I've been on wellbutrin xl, metoprolol, a beta blocker for heart rate associated with anxiety, and random benzos for about 5 years. I've been on and off of zoloft, which was rough. I take trazodone at night for sleep. And I've been on trintellix for a while now also, and I'm up to 20mg. Lately I've been so lethargic and having a hard time with any task, even getting dressed, brushing my teeth, much less actually cleaning up. I've also not been able to really get out of the house if I'm alone. I haven't had a xanax in over a week, so that's good, but idk what's going on. I've gained a ton of weight, constantly getting sick with something, and my skin looks terrible, and my eyes stay sunken in. I really want to come off of all my medications and rely on a more natural approach. I'm tired of feeling like a dead person walking around, and I want to feel things like I used to. I'm also running out of time to decide to quit everything and have another child. Where should I start tapering? Thanks for any advice.
  25. I have been taking Trazadone since January 2014. I started with .75 Traz and have been slowly tapering the past six months. I am now down to .38 Traz after making a cut 2 nights ago from .45 Traz.. I take it at night to sleep along with 7.5 Remeron. I have been doing well with sleeping on the .45 which I have been holding the past 2 months. Last night my sleep was very light and fitful after the cut. I doubt I got that much sleep. Also, this October I will be on year off Ambien 10 mg. I am looking for some encouragement from folks who have been down this road before with Trazadone. Any success stories out there? How did you feel along the way with tapering? How was your sleep? How did you feel one week off Traz, three weeks off, a month off?
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