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

Interested in more discussions like this? Go to the Depression & Anxiety Support Group.

Profile picture for Leonard @jakedduck1

@huxy
“Believe me when I say it is hard enough reducing by this amount! I’d hate to go any faster.”
How about going a little slower and making it easier.
I went off several medications so slowly I never had any symptoms at all.
You decreased your dose by about 25%, which is high. You say it’s “hard” that would indicate to me your tapering to fast.
There is a tappering method known as the 5-10% taper. It’s best if it’s done through a compounding pharmacy. Large tapers are better tolerated in the beginning but as your dose decreases if your taper isn’t adjusted withdrawal symptoms are more likely to occur.
Jake

Jump to this post

Thank you Jake! Really great advise/information.
Huxy

REPLY
Profile picture for huxy @huxy

I’m down to 37.5mg once a day and a 1/4 crumb once a day. This has taken one month of gradually reducing my prescription.
Anyone else trying to get off of Effexor ?

Jump to this post

I'm off. Its hell going through. Please know you are not alone. There will be light in the world again, but it may take awhile.

REPLY
Profile picture for sherry47 @sherry47

I'm off. Its hell going through. Please know you are not alone. There will be light in the world again, but it may take awhile.

Jump to this post

Thank you so much for your words of encouragement! No nausea today and plenty of happy energy. So different from yesterday.
I’ve Got to keep on going!
Thank you

REPLY
Profile picture for bud123 @bud123

Thank love for this informative article!

Jump to this post

Thank you for your tips! The struggle is real!

REPLY

I started tapering at 300mgs. 1 month at 150, one month at 75, one month at 37.5, stop. I thought l was going to die. I wanted to die. I postponed my final college degree module, cried, contemplated suicide, you name it. Too many doctors don't seem to know anything about tapering, because l could easily have killed myself to escape the pain.
I survived, but knew very little about what to expect, because neither did any of the experts responsible for my care. I was asked what l wanted to try. I AM NOT A DOCTOR. But l'm staying clean. I am not becoming a statistic. I am a bpd survivor.

REPLY

I have been tapering down from 150 mg of Effexor after several weeks at 37.5 mg., I am now on day three of not taking it at all. I’ve been managing the achy body with Tylenol all through the tapering. However, now I am experiencing insomnia and then when I finally fall asleep from exhaustion, I have crazy and slightly disturbing dreams so I wake up pretty anxious. That part is manageable. I am really struggling with the “swooshing” sounds in my brain. They are not painful but make is extremely difficult to concentrate and focus on computer work for my job. Also I am feeling nauseous so my brain wants me to eat all the time. Plus, I feel pretty weepy at times and get irritated easily. Any tips to get through this time? I know eating healthier and continue to exercise will help. Any other tips? Especially with the “swooshing” sound in my head? I am also considering taking Tylenol PM at night so I can fall asleep and stay asleep. Any advice on this plan? Thank you!

REPLY
Profile picture for adanaya @adanaya

I started tapering at 300mgs. 1 month at 150, one month at 75, one month at 37.5, stop. I thought l was going to die. I wanted to die. I postponed my final college degree module, cried, contemplated suicide, you name it. Too many doctors don't seem to know anything about tapering, because l could easily have killed myself to escape the pain.
I survived, but knew very little about what to expect, because neither did any of the experts responsible for my care. I was asked what l wanted to try. I AM NOT A DOCTOR. But l'm staying clean. I am not becoming a statistic. I am a bpd survivor.

Jump to this post

Hi @adanaya and welcome to Mayo Clinic Connect. You are quite brave to endure that! My goodness I cannot imagine the pain and suffering.

Here is an article on self care with BPD:
https://www.mind.org.uk/information-support/types-of-mental-health-problems/borderline-personality-disorder-bpd/self-care-for-bpd/
What are you currently doing to fight the mood swings and the ups and downs?

REPLY
Profile picture for seabrook22 @seabrook22

I have been tapering down from 150 mg of Effexor after several weeks at 37.5 mg., I am now on day three of not taking it at all. I’ve been managing the achy body with Tylenol all through the tapering. However, now I am experiencing insomnia and then when I finally fall asleep from exhaustion, I have crazy and slightly disturbing dreams so I wake up pretty anxious. That part is manageable. I am really struggling with the “swooshing” sounds in my brain. They are not painful but make is extremely difficult to concentrate and focus on computer work for my job. Also I am feeling nauseous so my brain wants me to eat all the time. Plus, I feel pretty weepy at times and get irritated easily. Any tips to get through this time? I know eating healthier and continue to exercise will help. Any other tips? Especially with the “swooshing” sound in my head? I am also considering taking Tylenol PM at night so I can fall asleep and stay asleep. Any advice on this plan? Thank you!

Jump to this post

Talking books.

REPLY
Profile picture for adanaya @adanaya

I started tapering at 300mgs. 1 month at 150, one month at 75, one month at 37.5, stop. I thought l was going to die. I wanted to die. I postponed my final college degree module, cried, contemplated suicide, you name it. Too many doctors don't seem to know anything about tapering, because l could easily have killed myself to escape the pain.
I survived, but knew very little about what to expect, because neither did any of the experts responsible for my care. I was asked what l wanted to try. I AM NOT A DOCTOR. But l'm staying clean. I am not becoming a statistic. I am a bpd survivor.

Jump to this post

I forgot to mention..I am going through withdrawal from Protiq, hence my symptoms.

REPLY
Profile picture for Amanda Burnett @amandaa

Hi @adanaya and welcome to Mayo Clinic Connect. You are quite brave to endure that! My goodness I cannot imagine the pain and suffering.

Here is an article on self care with BPD:
https://www.mind.org.uk/information-support/types-of-mental-health-problems/borderline-personality-disorder-bpd/self-care-for-bpd/
What are you currently doing to fight the mood swings and the ups and downs?

Jump to this post

It's a combination of CBT and talking books. I can't move because the mental pain is sometimes constant and unbearable, but having to follow a story, a life, facts, can keep things damped down. This condition does NOT get better as you age. We die, we take our own lives, we give up on there being any help, so we don't show any more. But we are still here and still going through this every single day. This has - merciful God - only happened once, but once makes me dread 'again'. My friend was here, she's a nurse, and we were tslking, but suddenly, l wasn't. I couldn't speak at all. I wasn't having a stroke, l simply couldn't speak. I could shake my head or nod, but no more. I couldn't write either. Interestingly, l could type. It was quite terrifying. Lucky it happeened at home. If it had happened outside? Phew! But it stayed with me for days. I could read, so l read. But l couldn't call for help. A scan revealed that no, l hadn't had a stroke. But something had happened. A harmless message from my brother's wife asking how l was, as she knows of my condition. Blameless and never caused me harm. The only thing therapist and GP thought was that my trauma was so bad that even such a tenuous contact drove me into - what happened. I have no contact at all now.
It is agonising pain. There is no treatment. At 66 l've been through an alphabet soup of medication, and all the additional agony of tapering off the worst ones. In my experience, love is the only treatment. Care. Kindness. That's the treatment.
Oh, yes, people fall to heroin, alcohol, all manner of drugs, but the best treatment is to know that someone really cares about you, and like everything else, even that's touch and go.

REPLY
Please sign in or register to post a reply.