Long term effects AFTER withdrawing from Effexor

Posted by DissidentDaughter @dissidentdaughter, Aug 4, 2018

I am wondering if anyone has had any experience like this. I weaned off Effexor three years ago. After doing so I have gradually developed what is now becoming debilitating chronic pain. I am wondering if there is any way that being on Effexor for 15 years could have caused me to develop this pain now that I am not on it anymore. Thanks for your thoughts. I can’t seem to find any direct related research on this.

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I was in 150 mg for 18 years. I went 150-0 in 3 months jumping off at 37.5. It’s been 22 months and I can absolutely say it’s been the hardest thing I’ve ever done. I’ve made tons of progress but still have a ways to go.
I wish I had have done some research and not just followed my doctors instructions to taper off.

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@abcxyz

Well, that’s reassuring as one positive from Effexor since inflammation is a major trigger for disease and cancer. I’ve been fighting my primary care doctor to let me wean down efffexor XR 75mg to 37.5mg and she’s like dealing with a timid child who doesn’t know if she should turn right or left so she chooses the stand still. It’s baffling to me how some of these MDs become doctors. I told her I was on 150mg for a few years and with my previous MD I simply said I want to get off this medication so cut my dose in half and they did and I was fine. Now, dealing with a new MD who acts like I’m asking for open heart surgery from a dentist when I ask for the lower dose. Unbelievable. I’ve heard it’s extremely difficult getting off Effexor completely so any recommendations for the weaning process is much appreciated. I don’t want the emotional numbness I’ve had since getting on the Effexor. It’s made me less social, more avoidant, less motivated to do anything, almost like I developed some kind of phobia about getting ready to go somewhere causing excessive worry about being late, which leads to delaying or refusing to start the process - therefor I end up exacerbating the tardiness fears by making myself late because I wouldn’t just get in the shower or whatever- so I either end up really late or missing out completely, but most often I cancel plans & appts I make because I don’t want to deal with the stress of getting ready & out the door. I never had any issues pushing myself to do things I didn’t want to do, but had to do for whatever reason, prior to getting on this dam* medication. I also had no idea it was extremely difficult to get off of and potential to cause permanent and/or long term problems once it’s out of the system. It’s infuriating to think about these unknowns never being remotely mentioned to me prior to the prescribing. As in there is no way I would’ve consented to taking it with the known risk/reward positivities. Especially, considering my depression was induced postpartum and exacerbated from high level long term stress from my job that finally made me turn to a doctor for medication to relieve depression/anxiety. Never had depression before giving birth and stress from my job was severe prior to, but never unable to cope with it until I had my son. I feel like a more appropriate plan would’ve been to advise me to take a leave of absence from work until I was able to address the postpartum depression via treatment. Not doing so was a a recipe for disaster walking me into the lions den of antidepressants. It’s effected my life in ways I will feel for decades to come and I wish I could go back and make the decision never to get on the medication in the first place. I knew better being in the medical field, but I thought there was no other way to keep all the things in my life manageable. Has anyone been able to get off Effexor and get back to who they were before beginning the medication?

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18.5 years on Effexor XR. lost a lot of my vision in the first 6 months and where glasses which have steadily gone up in changes. Now on 2+ to be able to see things non blurry. Managed to get down from 225mg one tablet at a time from three over the last 2-3 years. Stopped the last one 3 nights ago and the zapping of the brain is horrendous. At night in the dark, the brain zaps come with blue green light, like being zapped by actual power. Tearful for nothing at times as of today. Very very confused, not knowing what I am doing at times. Disoriented. All of the withdrawals appear to be getting worse with each day as of day 3 now. I did this for me. I have no money as I am on a govt payment, 61, with a number of chronic conditions and hospitalisations including surgery for recurring abscess formations (large pus collections abutting the liver apparently in my fat and skin, which have broken through my chole incision twice now and sent me straight to surgery for drainage, following 3 months of a none healing surgical wound now). Continuous infection symptoms 4 times in the last 3 months, with chills, weakness, aches, headaches etc, making a very pusy overfull abdominal dressing each time, but with no microorgansims found when tested???? High white blood cell count in urine and blood, and CT with contrast showing extreme inflammation at the base of the wound (and probably throughout the rest of the body at that). I just don't understand how all the signs of infection are there every few weeks, extra exudate is there, yellow/green and there can be no microorganisms found each of the 4 times this has happened in the past 3 months. Is my immune system picking up the culprit before it is sent to the lab and somehow erasing it? Is this an auto immune disorder? I know 20 years ago, the doctors were checking for lupus, but somehow this didn't go any further, due to other issues at the time. Well, I also stopped my Melatonin for sleep at the same time as I stopped my last Effexor three nights ago. I have no money as my entire payment now goes to rent, which keeps rising and I have to get food from food banks. No money for GPs or medications, so I had to stop my antis. Aside from that, I am also sick of being controlled by these medications and doctors who are being backed by pharmecutical companies to push these things. I want back control of my life. I hope these withdrawal symptoms will go away and I will find out who I am after 20 years and make my own decisions about ways to manage my depression/anxiety through diet, exercise, mindfulness, relaxation etc. I am considering taking one St John's Wort to counteract the withdrawals tomorrow as I've read these Effexor withdrawals may go on for months

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Stopping melatonin at same time as Effexor is maybe not the best action

I am reducing and have less side effects as I am doing it very slowly
I have been taking 7.5 ngs twice daily for weeks but will not reduce more until the zaps cease
The last small doses has been the most difficult to stop

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Definitely slow down the dose level when titrating off.
As Looplu 79 says, drop down dose , (with ever smaller Pill sizes) each time, as the side effects (withdrawal) effects begin to lessen.
Anyone still getting legacy side effects after a long & careful titration off? I am still getting allergic reactions over 2 yrs after a 3 yr titration off EFFEXOR / VENLAFAXINE . Including, swollen mouth / lips every day on waking & Blood spots on head. I have read it can take 4+ years for these legacy effects to stop. Any similar experiences? I seem to be very rare with this type of prolonged side effects issue.

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@simon007

Definitely slow down the dose level when titrating off.
As Looplu 79 says, drop down dose , (with ever smaller Pill sizes) each time, as the side effects (withdrawal) effects begin to lessen.
Anyone still getting legacy side effects after a long & careful titration off? I am still getting allergic reactions over 2 yrs after a 3 yr titration off EFFEXOR / VENLAFAXINE . Including, swollen mouth / lips every day on waking & Blood spots on head. I have read it can take 4+ years for these legacy effects to stop. Any similar experiences? I seem to be very rare with this type of prolonged side effects issue.

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I slowly halved my Effexor from 150 to 75 w/o any side effects and stayed with that about 5 months until I had a major anxiety attack and decided to go back up. I am 79 and I just want to be comfortable in the later years. I must be very fortunate not to have these terrible side effects.

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@david707

I slowly halved my Effexor from 150 to 75 w/o any side effects and stayed with that about 5 months until I had a major anxiety attack and decided to go back up. I am 79 and I just want to be comfortable in the later years. I must be very fortunate not to have these terrible side effects.

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I see a difference between side effects from withdrawal and return of anxiety
I would suggest a change of drug for anxiety which does not have the same effects as Effexor
I had no side effects when dropping dose of Effexor up to 37.5 mgs slow release daily I had been on 150 mg for 17 years
However once down to
Much smaller doses I experienced some side effects so am very slowly lowering dose
If you have been on Effexor for more than 5 years withdrawal effects are more pronounced

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@dquest20

Hi just doing researching again and saw your post from 2018, I too was on Effexor for 15 years, I weaned off it in Nov 2012 and by March 2013 was my first ER visit that started my eight year chronic pain journey that has destroyed my life, and left me a shell of a person, it has been the mystery of my lifetime, I'm a cancer survivor and fought hard in my twenty's to survive endometrial cancer, after that to a successful business owner, raised my family and enjoyed life and I did suffer from some depression and anxiety and had a few other health issues but not that took away my quality of life and now I am completely bedridden in eight years, I have been to over 30 different doctors trying to get help/answers with all the pain throughout my body, in eight years now I have been diagnosed with Lupus, Chronic Osteoporosis, Osteoarthritis, Cervical Disc Disorder with Radiculopathy, Intercostal Neuralgia, Bilateral Occipital Neuralgia, Costochondritis, Fibromyalgia, Chronic Migraines, Bile Reflux, Meningiomas in my brain, etc. it just goes on. I had none of this before except I did suffer from Migraines all my life. The Pain started in my left ribcage and spread from there, when I went off the Effexor I had gained some weight from it at 175 pounds I am 5 foot tall, my normal weight was about 130, now I only weight 85 pounds because I can't eat much of anything, I have weighed under 100 pounds for four years now, and I've had to have all my top teeth replaced because my jaw bone was shifting and cracking, I had so many procedures and two surgeries, nerve blocks, and trigger point injections 700+ in 8 years, with over 400 just in the last three years all over my body rotated biweekly and I have to be on pain medication and sleeping pills for years, I feel like I will die any day I'm 58 years old, For years Dr. would take blood tests, MRI's, CT's X-rays and tell me I was fine, bloodwork looks fine, test look fine, but I was in so much pain I couldn't stand it, I didn't know why I was loosing weight or feeling such bad pain, I was scared, most dr's made me feel it was all in my head and treated me unkindly, all I was asking for was help I was scared, until the damaged started to show up on the MRI's, labs etc. and my health begin deteriorating and now. I have brought it up many time with dr's I have seen about any connection to Effexor since I had such a hard time getting off of it, but I just get that blank stare or they can't say. I would really be interested to know if anyone else has had anything similar happened to them or someone they know.

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Hi @dquest20! Your experience sounds so similar to that of my fiancée. If you’re up for sharing, I’d love to know if you have an update. It’s so hard to watch my fiancée suffer and I am eager to learn anything at all that might help her. Thanks in advance and much love to you in your ongoing journey!

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