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Post Info TOPIC: Horrible Paxil experience
DJ


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RE: Horrible Paxil experience
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A few years ago my daughter was put on an SSRI because of something she was going through and it was a nightmare.  Then it was a nightmare to get her off of it.  I saw a documentary called 'Prescription Suicide" about how teens often go commit suicide when put on these.  I had no idea.  And as I am about to start treatment (hopefully next month) I decided not to use them.  I don't want to be depressed, but since my daughter reacted the same way you did to them, I am afraid I would too.  So I will have to just make it through without. 

Now I do know people who have used them successfully and the SSRIs have been helpful.  You just never know how your body will react to them.  But I don't want to chance it. Glad you were able to get off and are feeling better now. 



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Genotype 3.  Treatment started on 1/11/2013 with Ribavirin and Pegatron.  Week 4 UND.  Week 12 UND.  Ended treatment on 6/28/2013.  Six months post treatment 12/04/2013 SVR.



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Thank you guys, all of you, so much.  As we all do, I keep on keeping on.

Tim, you and I are both in the Antelope Valley, so you know this heat hasn't been helping.  Been about 106* - 111* daily for nearly 2 weeks!  Makes the dizziness and nausea worse.

 



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Geno 1a; VL 4.7 million in Feb 2012. Started PegIntron & Ribavirin 3-9-12. Added Victrelis 4-6-12. UND since Week 8. Stopped tx Wk 23. UND 4 Wks post-tx. Relapsed 12-weeks-post.

52 y/o F, started Epclusa 11-10-19, F0/F1.  EOT 2-1-2020. UND. All liver function tests normal.



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Judy,

Good grief, what a nightmare that turned out to be! Good thing you have Bri to take care of you.

You sure have a "full plate" with the tx and meds for sides, stay as strong as you are, wishing you the best for better days soon!

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"hrsetrdr"=Tim

Treatment halted on Aug.8,2012 due to vision problem.  6 month post tx labs

Aug.2013 SVR

Be strong when you are weak, brave when you are scared, and humble when you are victorious.
- Unknown

 

 



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Judy--you and Bri are the most amazing people. Such strength--glad you got off those AD's, you are on quite enough meds. Karen's suggestion about the B complex and Flax oil sounds pretty interesting. I would have tried it and will keep it in mind.

Keep strong--we are all here for you!!

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Diagnosed 1996 genotype 1b VL alot tx starting 12/23/11 Victrelis UND week 8!!! 28 weeks of tx

Completed tx 7/6/12--still UND!!!!



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Hi Judy-OMG you have been through a lot...Bri too!!!

Not sure what you can take while on treatment but B complex and Flax oil work pretty well for mild depression/anxiety-were recommended many years ago by my doc in lieu of allopathic drugs.  I know many people taking Flax Oil for depression and rave about the results...  

You are sure in need of brighter days...wishing you many to come.



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Geno Type A1- VL 16.2m - F1-F2 Moderate Fibrosis - Started treatment 4/16/13 Sofosbuvir/Ledipasvir 6 months -  UND week 4 (5/14/13) - EOT 10/1/13 - 12wk blood draw 12/20/13 UND - 24wk/final blood draw March 2014



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Judy S wrote:

Thank you guys, all of you, so much.  As we all do, I keep on keeping on.

Tim, you and I are both in the Antelope Valley, so you know this heat hasn't been helping.  Been about 106* - 111* daily for nearly 2 weeks!  Makes the dizziness and nausea worse.

 


 That's for sure, I've been having fantasies about that bucket of snow that kiwi is supposed to ship us, from...here:

snow.jpg

 

What a great lace to do a snow angel....can only do "dirt angels" right now here.  gen068.gif

edited to make the photo smaller!      



-- Edited by hrsetrdr on Tuesday 14th of August 2012 04:41:45 AM

__________________

"hrsetrdr"=Tim

Treatment halted on Aug.8,2012 due to vision problem.  6 month post tx labs

Aug.2013 SVR

Be strong when you are weak, brave when you are scared, and humble when you are victorious.
- Unknown

 

 



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Oh Judy you have really been through it! I'm so glad you are as strong as you are. You have taken all the hits this treatment can give. I'm gad you got through this one too!

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Kelly 2b dx 8/11. Tx begun 12/30/11. Apparently had it for decades.


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Thank you, Alan.  If this doesn't kill me, it will make me one heck of a lot stronger, lol.  



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Geno 1a; VL 4.7 million in Feb 2012. Started PegIntron & Ribavirin 3-9-12. Added Victrelis 4-6-12. UND since Week 8. Stopped tx Wk 23. UND 4 Wks post-tx. Relapsed 12-weeks-post.

52 y/o F, started Epclusa 11-10-19, F0/F1.  EOT 2-1-2020. UND. All liver function tests normal.



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Judy, are you the strongest person on eath? I think you are. And Bri is running a close second. You two amaze me. Good call on the ADs. Just do what makes the most sense to you. You are getting pretty good at this. I know you listen to your doctor. We all do. But you are also starting to make up your own mind, based on all the things you know. This is the best treatment of all.

Alan



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Geno 1A  Started Pegasys/Ribavirin/Incivek Nov. 20, 2011 .  Completed July 28, 2012 (36 weeks). For a treatment history, see:  https://jshare.johnshopkins.edu/xythoswfs/webview/_xy-9921874_1

SVR on January 14, 2013!!



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hi! i got SSRi(anti depressives..brand name setraline) some time ago and i only had one and felt like crap i did not eat and sleep for 2 daysomg.gifwas getting crazy so i stopted..never again!! i take a valium sometimes when i feel anxious and thats it..i try to keep as simple as possible! no more crazy stuff in my brain im already crazy enough without those pills!!bleh treatment WILL finish and i dont count the days..i make the days count!



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hep c 1a on triple therapy with incivek UND at week 12 ,week 24...going for 48 weeks.



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This tx (treatment) is pure hell, but together with the Paxil my dr put me on, I have been nearly suicidal.  If I didn't have Bri to care for, there's no telling what I may have done; it's been maddening and PURE HELL.

 I had a basic understanding of how ADs (antidepressants) affect the Serotonin receptors in the brain.  From the moment I started Paxil 2 weeks ago, I developed SEVERE anxiety, insomnia, nausea, uncontrollable body movements, tremors, restlessness, a severe inability to sit, stand, or lay still.  I was going CRAZY.  I couldn't eat and eventually couldn't walk or breathe properly; I ended up in the hospital for the day again via ambulance on Aug 4.

 My dr reduced my Paxil dose to half, 1 week ago (hospital day when I nearly quit tx) to wean me off.  I have stopped completely on Saturday (2 days ago).

Not wanting to be ignorant about things I don't fully understand, I did more Paxil research to educate myself better.  I'm glad I did.  MANY patients have the SAME reaction to Paxil and any ADs.  Here is why:

 Please know that many people have this reaction to SSRIs when they first start them. The digestive tract has more serotonin receptors than anywhere else in the body (even the brain), so many people feel nauseous when they first start them, since the receptors are dealing with more serotonin than normal.

The reason you feel anxious (tremors, insomnia, restlessness) when starting them is as follows: the theory is that those with depression (and possibly anxiety) have smaller amounts of serotonin circulating in the brain. Because of that, the brain has, over time, increased it's numbers of receptors, hoping to mop-up all available serotonin it can find.

When you start taking SSRIs, the medication increases the amount of serotonin available to the receptors. This wouldn't be so bad if you had a normal number of receptors, but if you have a huge number, your system is suddenly flooded with serotonin. In normal doses, serotonin "activates you" and makes you feel good (hence people with depression feel lethargic and inactive). In too high doses, it "over-activates" you - the symptoms you describe.

Two things to note: 1) the symptoms go away after a short while - say, a week or two after beginning the drug. This is how long it takes the number of receptors to down-regulate to a normal number. 2) the ironic thing is that people who get this reaction may be exactly the people who NEED it most, for the reasons outlined above.

It's a shame, I agree, because the side effects are miserable. Even though I'm a doctor, I'm on an SSRI, too (for anxiety), and I had the same reaction when I first started. (So, just so you know, doctors don't only prescribe these meds, we take them, too!)

My own doctor put me on a low-dose benzo for the first week, and also had the pharmacy compound down the drug so that each pill contained only a very small amount - eg. instead of starting with 10 mg of Celexa, I started with 2 mg, then increased to 4 mg, then to 6 mg, until I worked up to 20 mg. Ask your doctor to try this for you.

Unfortunately, I'm not sure you'll notice much difference in side effects between the different SSRIs. As I said, the side effects are actually a sign the drug is working, and despite the different names, they all work more-or-less the same.

The withdrawal side effects are true with regard to Paxil (though I've had patients comment on similar withdrawal from Celexa and Effexor - it may be the same for all of the SSRIs). The drug companies call it a "discontinuance syndrome" as opposed to withdrawal, but whatever you call it, it's miserable. I've missed a few pills now and again, and I know what you're talking about.



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Geno 1a; VL 4.7 million in Feb 2012. Started PegIntron & Ribavirin 3-9-12. Added Victrelis 4-6-12. UND since Week 8. Stopped tx Wk 23. UND 4 Wks post-tx. Relapsed 12-weeks-post.

52 y/o F, started Epclusa 11-10-19, F0/F1.  EOT 2-1-2020. UND. All liver function tests normal.



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I agree with you; I don't need ANY more craziness in my brain, thank you very much!  The Interferon, Ribavirin, 44 weeks of Victrelis, Neupogen, and Procrit are plenty for me, gooooooodness!!!!   Now, I take Ativan when I need to for anxiety.  That's it.  No more ADs.



-- Edited by Judy S on Monday 13th of August 2012 07:44:06 PM

__________________

Geno 1a; VL 4.7 million in Feb 2012. Started PegIntron & Ribavirin 3-9-12. Added Victrelis 4-6-12. UND since Week 8. Stopped tx Wk 23. UND 4 Wks post-tx. Relapsed 12-weeks-post.

52 y/o F, started Epclusa 11-10-19, F0/F1.  EOT 2-1-2020. UND. All liver function tests normal.

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