Tips on minimizing withdrawal symptoms from Effexor (aka Venlafaxine)

Posted by richyrich @richyrich, Nov 2, 2016

I have been taking Effexor/Venlafaxine for years and tried to get off it a few times but each time I try to give up the chemical withdrawal symptoms are a horror story and I give up giving up. Anyone got any tips or tried and tested strategies? Thank you

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I am going cold turkey off of venlafaxine xr 225 mg. Its been 5 days I do take trazodone 25 mg to help sleep. What can help with the physical symptoms please ?

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Not a good idea to go off Effexor cold turkey. Talk to your doctor and taper very very slowly.

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Daily walks definitely helped. And it's a good routine to have no matter what.

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Profile picture for secretwhitepop @secretwhitepop

I’ve been diagnosed with something called PPPD. And I want to say Mayo Clinic is studying it as well. Unfortunately I’m at work (with kids) and can’t remember what PPPD stands for... but the last work is dizziness.

Vertigo stinks! And anxiety plays a role.

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Do you still have PPPD? Have you found anything that works? I was diagnosed with it back in 2023. So far nothing works. I just received 31 Botox injections around the crown of my head yesterday and they say it will take 2-3 weeks to see any results. Fingers Crossed!!

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Profile picture for angel70 @angel70

I am going cold turkey off of venlafaxine xr 225 mg. Its been 5 days I do take trazodone 25 mg to help sleep. What can help with the physical symptoms please ?

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Hello @angel70 and welcome to Mayo Connect. As was mentioned by @mialucy123, it is not a good idea to go off Venlafaxine cold turkey. I would encourage you to contact the doctor who prescribed this medication and ask for a titration schedule to reduce the amount you take over several weeks.

You mention having "physical symptoms." Can you explain what those are? Have you contacted your doctor yet?

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Profile picture for coloradogirl @coloradogirl

So, I just finished this process with Zoloft (sertraline) and here are some things that worked for me. Your mileage may vary, but hopefully these are low risk for you to try.

1) You may need to ask your doctor for a slower tapering program than other patients. Some people are just more sensitive to dosage changes. Be aware that symptoms will get better, then may reappear each time you taper. AAFMA (practice group of family physicians) says that the symptoms typically last 1-2 weeks and as long as 4 weeks, so I just kept reminding myself that it was temporary.
2) Be watchful for things that make your symptoms worse. For example, caffeine seems to trigger the brain zaps for me (still, even after being off for several weeks), so I cut back my caffeine intake. I didn't give it up completely (because I still need to function), but cut back on how much real coffee I was drinking, mixed decaf with regular, and switched to tea sometimes. In the end, I probably cut my daily caffeine intake in half, and it did help quite a lot.
3) Ibuprofen or other pain reliever can help with the flu-like body aches.
4) Benadryl helped with the brain zaps.
5) Exercise helped with both. Even if I wasn't up to a run, a few blocks of walking would settle down the symptoms for a while at least. (Then, when they come back, just take another walk. We took a lot of walks for a while there).
6) Get enough sleep. As I came down off the meds, my normal sleeping patterns returned, which was great, but it did mean that I needed to plan time to let my body rest.
7) Pay attention to your diet. Your brain uses carbs to make seratonin, so now is not the time to go on the Atkins diet. Eat well and make sure you're getting enough healthy carbs. You may crave sweets; I certainly did. I tried to counteract this by having bananas, graham crackers, and other healthy things I could snack on instead of sticking my head in a birthday cake like I seemed to want.

No lie - it's a painful process, but this did really help make it easier. Also, at a certain point, when I was down the below the normal starter dose, I just ripped off the bandaid and went to zero. At that point, it felt like each taper was just prolonging the suffering. Don't just go cold turkey from your current dose, though, as that can be dangerous. Also, don't add any supplements or substitutes for the SSRI without talking to your doctor first (also dangerous).

And of course, watch for the return of depression / anxiety type symptoms. For a while it was hard to tell whether I was tired because of the change in meds or because my depression was returning. I figured as long as I felt okay enough to function and wasn't thinking about being harmful to myself or anyone else, I could play it out and see. It turned out to be the meds and on the other side, I can see that I was more worried about it than I needed to be.

I wish you the best of luck and a healthy life.

Mardee

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This is great thanks for sharing. A symptom diary can be very helpful also

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Profile picture for njoys @njoys

It is possible to do. Be aware that the beads inside a capsule may differ in number, they also differ in size. It is tedious to count them, and to return them to empty capsules before taking. But it is possible if one is sufficiently motivated.

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You can weigh them with a jewellery scale that weighs in milligrams

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It really is not a good idea to just stop taking (cold turkey), venlafaxine. I tried to gradually stop taking over a year ago, for the first time. Despite the fact I was doing do gradually, I had a few days when I felt really depressed, and was afraid that I was going back to it. I also had horrible brain zaps, and pains all over the place. There didn’t seem to be anything I could do that would help. My G.P. simply said that I knew more about the process of reducing the dose, but that she would be happy for me to stay on it permanently. In the end, the last straw came when, having reached a daily dosage of 75 mgs, (I had originally been on 300 mgs), I took a 75mg tablet on alternate days. I later found that this was the worst thing I could have done. I came out with the most horrible skin condition, all over me - literally. It was in my ears, right down inside my ear canals, up my nose, etc. I’ve had this condition ever since. However it started to improve, and I decided to go ahead with my second attempt to reduce the dosage, having had to go back to my original dose. Everything is now going well. I would really recommend that you buy the book ‘The Maudsley Hospital Deprescribing Guidelines for Anti-Depressants, Benzodiazepines, Gabapentinoids, and Z-Drugs’.
This book is by Horowitz and Taylor. I don’t get anything for recommending this book, it’s just brilliant, and guides you how to successfully reduce your dosage. Venlafaxine is one of the ‘highlighted’ medications in the book. The two authors have now written the Prescribing Guidelines book, and quite honestly, every G.P. surgery should have a copy of each. Good luck!

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Profile picture for Gail Benson Ledesma , Alumni Mentor @gailb

@lindmissi

Hello and welcome to Mayo Connect. I'm a Volunteer Mentor with Mayo Connect; I am not a medical professional and I can only offer you my personal experience. We're all here to share our experience in hopes of helping others with similar situations, understanding that each individual is different and what helps or hinders one person may not apply to other people.

I was prescribed Gabapentin 300 mg 3x day, for my chronic back pain. I found during the 6 months I took it that I was losing my memory. Large amounts of time disappeared and I was always in a brain fog. I thought I was getting Alzheimers. I was just goofy, and at one point had a small fender bender, im sure due to the Gabapentin. I decided that day to get off it. It seems as if doctors, mine was a pain doctor, prescribe Gabapentin for everything now. When I told my pain doctor I wanted to stop taking it, he got mad at me and wanted to know why. I explained my reaction to it and said k didn't think it was helping me. He would not help me withdraw and said I should just quit. I knew that was wrong from what i had read on Mayo Connect. After I withdrew with the help of my pharmacist over 3 months, I discovered that my pain improved. I think it made me feel more pain than i was actually having. I will never take Gabapentin, Neurontin, or Lyrica which are all related again. I think its a bad drug personally. I was even wondering if drug companies were giving doctors kickbacks for prescribing those medications. Probably just my imagination. Good luck with finding out what you need to help you. Please let us know what you find out from your doctor about why he has prescribed it for you.

Gail B
Volunteer Mentor

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I am on 75 mg plus 37.5 mg Effexor. 300 mg gabbapentin 2 x day for back pain. I too wonder if drs get a kickback to prescribing certain meds…. Especially the newer ones that are so expensive. My psychiatrist prescribed rexulti which was 250.00 with ins. I’m on a very tight fixed income, so that was out of the question! She switched to latuda, but I can’t take it, so not taking either one. Anyway, I am trying to wean off Effexor to get on cymbalta which they say is better for pain? ( I have severe arthritis in my back and nerve pain that radiates down to my ankle). I hate gabbapentin, but lyrica didn’t help.

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Profile picture for careth2 @careth2

Hi there! I am new to Connect, but hopefully can offer some insight. I DID go off 150 Effexor XR (name brand) COLD TURKEY on January 2016. I survived it, but will never in my life EVER go off ANY antidepressant cold turkey. I had taken Effexor for at least 8 years, Zoloft prior to that and and Imipramine (sp?) as the first antidepressant (in all 25+ years on antidepressants.) It all started with running out of meds over a long weekend and deciding it was time to try to get off antidepressants to see how I would do. Since I had recently retired from teaching, thought this would be an ideal time to give it a go. In addition, Effexor just wasn't helping all that much anymore (I thought.) The first 3 days I felt like I was going to die! When I realized that I wasn't dying, decided to keep going to get it all over with. In addition to the symptoms you have heard about, I had deep bone/joint pain that felt like I was being pinched with clamps. Also had skin sensations and peeling, and noticed a strange smell on my skin. Each day got a little better and by the 3rd week started to function a bit more normally. I was very emotional, however, which caused my family great concern. Well, to make a long story short, the depression crept back in full and I am still trying to get my life back. I did everything I could to stay stable, including herbal supplements and took a vacation where I hiked 6 miles daily for 9 days on hilly, rocky terrain. I finally had to accept that I'm a person who will need antidepressants for the rest of my life. With the help of a PCP and counselor, I am on my 3rd antidepressant & may need to resort to going back on Effexor, because nothing seems to be working. All in all, in my opinion, the chronic depression is worse than the withdrawal symptoms that do eventually end. If you are a person with situational depression, you may be successful weaning off Effexor gradually. If I were to do it again, that's what I would do (while replacing Effexor with something else.) Here are the things that helped me with the physical withdrawal symptoms:
1. Get plenty of sleep/rest.
2. Eat a very well-balanced diet (this is not the time to worry about your weight.) Lots of soup & easy to digest foods the 1st few days.
3. Drink plenty of water, including coconut water.
4. Have a glass of wine in the evening (if advisable.)
5. Get outside and walk or other excersize (the warm sunshine will feel good!)
6. Hot yoga 3-4 times per week. Stay in class even if you feel nauseous & can only do a few postures.
7. Soak in a hot tub (with bath salts if available.)
8. Use a good moisturizer on face & body several times per day.
9. Get several professional massages.
10. Take Tylenol for muscle pain, if OK on your stomach.
11. A heating pad is also helpful at bedtime or during naps.
12. If you are single & live alone, make sure a few trusted friends/family members know what you are doing.
13. In general, be kind & gentle to yourself.
14. NEVER give up! Keep going, even when you don't feel like it (which will be often.) YOU ARE WORTH IT!!!

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Thank you for such a thorough post. I haven't been able to figure out why I smell. I thought it was the heat. You are the first person to mention a similar problem. Now I can relax about it.

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