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tanos75: Late Paroxetine Reinstatement after 7 months – any realistic chance of helping PAWS/PWS?

Featured Replies

Hi everyone,

I would really appreciate your thoughts on whether a late Paroxetine reinstatement makes sense in my situation and whether anyone has seen success in a similar case.

Here is my history:

  • Took Paroxetine 30 mg for about 2 years.

  • After reducing to 20 mg, I developed what I believe was PAWS/PWS after about 3 months.

  • I increased back to 30 mg and improved for about 3 months, but then the symptoms gradually returned despite being back on the full dose (possible tolerance/tachyphylaxis).

  • My doctor increased me to 40 mg, then I was rapidly tapered to 0 mg over only 7 days. My last dose was 25 December 2025.

  • Since then I have been suffering from severe withdrawal symptoms.

After stopping Paroxetine, I tried two medications in an attempt to become functional again:

  • Venlafaxine, up to 150 mg – it made me significantly worse, so I discontinued it.

  • Escitalopram (10 → 5 → 2.5 mg) – it also failed and I stopped it on 16 June 2026.

I am currently taking Pregabalin 300 mg/day.

Initially, Pregabalin helped a lot with the anxiety, overstimulation and constant “fight or flight” feeling. Unfortunately, over the last several weeks it seems to have lost much of its effectiveness and I am now back to severe anxiety, panic waves, depression and extreme CNS sensitivity.

One psychiatrist has suggested trying a late Paroxetine reinstatement. Two possible approaches were discussed:

  1. Start at 10 mg, then increase very slowly.

  2. Start at 0.2 mg and increase in tiny increments (about 0.2 mg at a time).

My questions are:

  • Has anyone here successfully reinstated Paroxetine after being off for around 7 months?

  • Is there still a realistic chance that reinstatement could improve PAWS/PWS at this stage?

  • Does my previous apparent tolerance (“poop-out”) make success less likely?

  • Given my history, would you personally consider a very tiny test dose more reasonable than starting at 10 mg?

I understand nobody can give medical advice. I’m mainly looking for experiences from people who have been through something similar, especially with Paroxetine/Paxil and late reinstatement.

Thank you for reading.

Paroxetine 30 mg × ~2 years. Developed PAWS after dose reduction and subsequent tolerance (“poop-out”). Rapid 7-day withdrawal (last dose: 25 Dec 2025). Failed trials of Venlafaxine and Escitalopram. Pregabalin 300 mg/day. Severe PAWS/PWS. Considering late Paroxetine reinstatement (7 months off).

Welcome to the forum!

 

This is a volunteer-run, community forum aimed at helping those who are tapering and/or experiencing difficulties with psychiatric medications and withdrawl syndrome. We are not medical professionals and cannot offer medical advice. We simply offer support and opinions which you could use as talking points with a medical provider knowledgeable in withdrawing off psychiatric medications.

 

Please familiarise yourself with the forum rules and the disclaimer located here: Guidelines

 

Please make sure your signature is kept up to date with your drug history. This will allow members to see some basic information about your drug history and situation so that they may help you best. Information on how to do this is located in the FAQs section above, but here is a direct link: Update Signature

Once this is done, future posts made by you will have this signature turned on by default. For this reason please keep it clear but condensed as possible.

Please use the format outline here Preferred signature/drug history format


I'm so sorry to read about the tough time you've had recently you will find plenty of support here for sure.

14 hours ago, tanos75 said:

I would really appreciate your thoughts on whether a late Paroxetine reinstatement makes sense in my situation and whether anyone has seen success in a similar case.

Here is my history:

  • Took Paroxetine 30 mg for about 2 years.

  • After reducing to 20 mg, I developed what I believe was PAWS/PWS after about 3 months.

  • I increased back to 30 mg and improved for about 3 months, but then the symptoms gradually returned despite being back on the full dose (possible tolerance/tachyphylaxis).

  • My doctor increased me to 40 mg, then I was rapidly tapered to 0 mg over only 7 days. My last dose was 25 December 2025.

  • Since then I have been suffering from severe withdrawal symptoms.

I think it possible you hit tolerance or gained an irritation to the drug due to moving the dose around suddenly. The subsequent increase to 40mg followed by a rapid taper would have been very hard on your nervous system which was already senstive. Each time we make a move like this is causes more and more problems. Hypersensitivity and kindling

14 hours ago, tanos75 said:

After stopping Paroxetine, I tried two medications in an attempt to become functional again:

  • Venlafaxine, up to 150 mg – it made me significantly worse, so I discontinued it.

  • Escitalopram (10 → 5 → 2.5 mg) – it also failed and I stopped it on 16 June 2026.

It is common for the doctors to try to treat the symptoms of WD with more drugs, this almost always makes things worse unfortunately causing more Kindling.

14 hours ago, tanos75 said:

I am currently taking Pregabalin 300 mg/day.

Initially, Pregabalin helped a lot with the anxiety, overstimulation and constant “fight or flight” feeling. Unfortunately, over the last several weeks it seems to have lost much of its effectiveness and I am now back to severe anxiety, panic waves, depression and extreme CNS sensitivity.

I know @RachelSusan was in a similar boat and started Gabapentin to treat WD symptoms. I think she stablised on that and Zoloft before tapering sucessfully off the Zoloft, she has now just started tapering from Gabapentin. So different drugs but an example of someone taking both a Gabapentinoid and an SSri at the same time.

14 hours ago, tanos75 said:

My questions are:

  • Has anyone here successfully reinstated Paroxetine after being off for around 7 months?

  • Is there still a realistic chance that reinstatement could improve PAWS/PWS at this stage?

  • Does my previous apparent tolerance (“poop-out”) make success less likely?

  • Given my history, would you personally consider a very tiny test dose more reasonable than starting at 10 mg?

No one can know for sure what would be the best move for you. You are certainly suffering from an injury caused by all the different events your nervous system has had to endure, this will take time to heal, more drugs won't solve this.

However some of what you are suffering with is likley WD from Paroxetine, so adding in some of this drug may answer the brains dependance on it and cushion the WD for you.

I think there certainly is a chance a RI would help, but it may also worsen you. Ultimately you have to decide if this is something you would like to try.

My thoughts would be if you wanted to RI I would only try a very low dose. Here is our guide the RI. Reinstating an Antidepressant

 

In the mean time this is what I would do if I were you:

 

-Stay Hydrated 

 

-Eat a good clean whole food diet, avoiding processed foods and sugars.

 

-Stay away from caffeine, alcohol and antihistamines and any other psychoactive substances.

 

Supplements are to be avoided initially, as they often irritate our nervous systems. Try to get your nutrition through food.

 

Down the line, you may wish to introduce Fish Oil and Magnesium. Those who can tolerate them have found them calming to the nervous system. Be careful try one at a time and start low and see how you get on should you choose to try them.

 

A daily walk is very important as much as you can manage, if you can manage it. Gets you your fresh air and Vitamin D does wonders for your mind!

 

You are very welcome here and I hope you find the site supportive.

I’m not a medical professional and cannot offer medical advice. I only offer my thoughts as support. Please speak to your health practitioner about your care. This is a peer site where we support each other on our taper/recovery journeys. 

 

If you are from the UK please make sure you fill in a 'Yellow Card' report for the MHRA. It is you doing your bit to help make a difference.

Please take the time to do it today 🙂 https://yellowcard.mhra.gov.uk

For US members details here.

  • Chippy changed the title to tanos75: Late Paroxetine Reinstatement after 7 months – any realistic chance of helping PAWS/PWS?
  • 1 month later...
  • Author

Hi everyone,

I’m struggling with persistent symptoms after rapidly stopping paroxetine in December 2025, followed by trials of venlafaxine and escitalopram. I stopped escitalopram in June 2026. A brief reinstatement of 1 mg paroxetine in late August was followed by severe akathisia, panic and breathing discomfort, so I stopped after four days.

I currently take 350 mg pregabalin daily, which helps with sleep, but I still experience sudden waves of physical anxiety without an obvious trigger.

My main symptoms are chest tightness and a frightening feeling that my breathing isn’t right. I automatically focus on my breathing and repeatedly “check” that I’m getting enough air by taking deep breaths, yawning or clearing my throat. My pulse can stay normal even during intense episodes.

My doctor suggested 10–20 mg propranolol. Has anyone had good experiences with it during antidepressant withdrawal—especially for chest tightness, breathing discomfort and constantly monitoring your breathing, rather than just a racing heart?

Experiences alongside pregabalin would also be helpful. I’d appreciate hearing about both benefits and any worsening or side effects. I’ll discuss dosing with my doctor; I’m mainly looking for personal experiences.

Thank you!

Note: This post was generated with AI assistance because I’m not a native English speaker. I’ve shared my full history and current situation in the chat, so the AI has the context to help describe what I’m experiencing.

Paroxetine 30 mg × ~2 years. Developed PAWS after dose reduction and subsequent tolerance (“poop-out”). Rapid 7-day withdrawal (last dose: 25 Dec 2025). Failed trials of Venlafaxine and Escitalopram. Pregabalin 300 mg/day. Severe PAWS/PWS. Considering late Paroxetine reinstatement (7 months off).

1 hour ago, tanos75 said:

I’m struggling with persistent symptoms after rapidly stopping paroxetine in December 2025, followed by trials of venlafaxine and escitalopram. I stopped escitalopram in June 2026. A brief reinstatement of 1 mg paroxetine in late August was followed by severe akathisia, panic and breathing discomfort, so I stopped after four days.

I'm sorry that your attempted reinstatement was so difficult.

1 hour ago, tanos75 said:

My doctor suggested 10–20 mg propranolol. Has anyone had good experiences with it during antidepressant withdrawal—especially for chest tightness, breathing discomfort and constantly monitoring your breathing, rather than just a racing heart?

Experiences alongside pregabalin would also be helpful. I’d appreciate hearing about both benefits and any worsening or side effects. I’ll discuss dosing with my doctor; I’m mainly looking for personal experiences.

I tried 10 mg propranolol one time for physical symptoms of anxiety in WD, and didn't find it helpful. This forum generally advises against using beta blockers because we have seen that it can cause a worsening of symptoms in folks with sensitive nervous systems.

Just generally speaking, I know when you're feeling awful it's tempting to try to find a quick fix, often by talking to your doctor about other meds. Unfortunately in WD, there really are no quick fixes, and often those who experiment with different drugs, supplements, etc, end up making themselves worse. I would really advise you to stop looking for another drug that will help with your symptoms and just trust that time and stability will lead to healing 💜

I’m not a medical professional and cannot offer medical advice. I am new to this journey and my thoughts are based only on my personal experience with psychiatric drugs. This is a peer site where we support each other on our taper/recovery journeys. 

Current regimen:

Cymbalta - 90 mg/day

Seroquel - 12.5 mg/day

*holding to stabilize as of Apr 2026

 

History:

Seroquel - up to 50 mg as needed for sleep (generally 6.25-12.5 mg a few times a week, though sometimes more) - 2009 (ish) to present

Cymbalta - 60 mg/day, periodically down to 30 mg/day - May 2014 to May 2025

Clonazepam - up to 1 mg/day as needed - March to May 2025, quick taper off

Zoloft - 150 mg/day - May 2025 to Aug 2025 (quick cross-taper from Cymbalta)

Pristiq - 50 mg/day from Aug 2025 to mid-Oct 2025 (quick cross-taper from Zoloft); 100 mg/day from Oct 2025 to Dec 2025; back down to 50 mg/day from Dec 2025 to Jan 2026

Lyrica - 200 mg/day - Nov 2025 to Jan 2026 (quick taper off from mid-Jan to early Feb 2026 due to severe depressive symptoms)

Cymbalta - 60 mg/day - Jan - March 2026; up to 90 mg/day from March to present

 

  • Author

Hey,

thank you so much for your answer!

Pregabalin is the only med that does not work by affecting serotonin levels that I tried so far and it really helped me. In fact I was feeling pretty good in the beginning until I probably built up a tolerance very quickly. That gives me hope that another med might help me too. 

It’s always those episodes of anxiety (with tightness in the chest, laboured breathing and a focus on my breathing) that hold me back time and again. If I could somehow make these episodes feel less threatening, I’d feel so much better straight away.

I’d be interested to know: has the forum also noticed that pregabalin makes the symptoms of WD worse?

Paroxetine 30 mg × ~2 years. Developed PAWS after dose reduction and subsequent tolerance (“poop-out”). Rapid 7-day withdrawal (last dose: 25 Dec 2025). Failed trials of Venlafaxine and Escitalopram. Pregabalin 300 mg/day. Severe PAWS/PWS. Considering late Paroxetine reinstatement (7 months off).

3 hours ago, tanos75 said:

I’d be interested to know: has the forum also noticed that pregabalin makes the symptoms of WD worse?

I tried pregabalin for anxiety symptoms before I understood that I was in WD. I reacted very badly to it, but unfortunately kept trying it because my doctor told me that I just had to increase the dose. I found that it affected my sleep for the worse -- my sleep became very broken -- and gave me terrible depressive symptoms, brain fog, and anhedonia. I also had SI for the first, and only, time in my life. I ended up tapering off rapidly from 200 mg and was very physically sick for several weeks afterwards, which has certainly contributed to my current protracted symptoms.

No matter what receptors any psych drug affects, we cannot predict how an already sensitized nervous system will react. Trying any drug is like playing with fire unfortunately.

I’m not a medical professional and cannot offer medical advice. I am new to this journey and my thoughts are based only on my personal experience with psychiatric drugs. This is a peer site where we support each other on our taper/recovery journeys. 

Current regimen:

Cymbalta - 90 mg/day

Seroquel - 12.5 mg/day

*holding to stabilize as of Apr 2026

 

History:

Seroquel - up to 50 mg as needed for sleep (generally 6.25-12.5 mg a few times a week, though sometimes more) - 2009 (ish) to present

Cymbalta - 60 mg/day, periodically down to 30 mg/day - May 2014 to May 2025

Clonazepam - up to 1 mg/day as needed - March to May 2025, quick taper off

Zoloft - 150 mg/day - May 2025 to Aug 2025 (quick cross-taper from Cymbalta)

Pristiq - 50 mg/day from Aug 2025 to mid-Oct 2025 (quick cross-taper from Zoloft); 100 mg/day from Oct 2025 to Dec 2025; back down to 50 mg/day from Dec 2025 to Jan 2026

Lyrica - 200 mg/day - Nov 2025 to Jan 2026 (quick taper off from mid-Jan to early Feb 2026 due to severe depressive symptoms)

Cymbalta - 60 mg/day - Jan - March 2026; up to 90 mg/day from March to present

 

19 hours ago, SarahMc said:

Trying any drug is like playing with fire unfortunately.

Wise words, worth taking very seriously

I’m not a medical professional and cannot offer medical advice. I only offer my thoughts as support. Please speak to your health practitioner about your care. This is a peer site where we support each other on our taper/recovery journeys. 

 

If you are from the UK please make sure you fill in a 'Yellow Card' report for the MHRA. It is you doing your bit to help make a difference.

Please take the time to do it today 🙂 https://yellowcard.mhra.gov.uk

For US members details here.

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