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AD=Placebo?


hugugh

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I've been slightly obsessed and majorly confused with this article since I found it:  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2253608/

 

I don't understand how drugs with such terrible side effects and with very little/no efficacy were approved for use and became so popular throughout the world.  I am not a conspiracy theorist so I'm having a hard time wrapping my head around the idea that anti-depressants might just be one giant scam between pharmaceutical companies, regulatory agencies and doctors.  How is this possible?  If this research is real (and it sure looks convincing) and antidepressants really are no better than placebo, then if the research was not muddled and hidden, my poor daughter would have been saved from years of torment that almost took her life.  It makes me want to tear my hair out thinking about this.

 

Has anyone seen this research?  Opinions? 

Daughter's Med History: 

Zoloft (25 mg-200mg) 2019-2022.  Cold turkeyed April 2022

Guanfacine (1mg-4mg) 2021-2022.  Tapered off May 2022

Lamictal (low dose) 2021 for brief period

Abilify (can't remember dose) 2021-2022 

Seroquel 2022 (225 mg):  Cold turkeyed April 2022

Naltrexone 2022 (brief period -stopped cold turkey)

Lexapro (5mg) 2022:  Started to help with withdrawal symptoms.  Only on for 2 weeks. 

Med free as of May 2022

 

 

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What I would like to say is that at least you know now.  You did what you did at the time, with the knowledge you had at the time. 

 

  • You did what you did because you care about your daughter and thought you were doing the right thing
  • You have more information now
  • You now know how to find information before deciding on what action to take
  • You are now better able to make informed decisions
  • You are doing the best you can

 

This is something that I think a lot of us have trouble getting our heads around.  And I think that the anger we have about it is warranted.  I, too, am not a conspiracy theorist, but from what I have learned since joining SA at the end of 2015, not just about psychiatric drugs but also about other drugs (statins, diabetic drugs) and the "research" results, I have become very cautious about everything that I read/hear.

 

It's a horrible way to be, not knowing what/who to trust but I have started questioning anything that a doctor suggests.  For example, I had a pain in my upper right quadrant and had an ultrasound that didn't show anything.  The blood test showed some markers for inflammation so she wanted me to take fluoroquinoline antibiotic.  I know about possible issues with this drug from what I had read here at SA so I did more research.  It turns out that there are 3 FDA warnings about this drug.  One of them is that older people (I was about 61 or 62 at the time) are at a higher risk of ruptured tendons.  When I gave this information to the doctor she said, oh but that is only x% (I think it was about 1%).  Things that I thought about:  I snapped an ankle ligament in my mid 30s and have issues with it ever since, I might be in that 1%, how many people get a ruptured tendon and it is not attributed to the drug (I had raised blood pressure after increasing my Pristiq from 50mg to 100mg and the doctor who prescribed it did not make the connection between that and the blood pressure; it wasn't until years later that I made the connection myself).

 

Anyway back to the pain.  I refused to take the fluoro and asked for a different antibiotic but she said that the fluoro was the one they give for what I had.  She said okay then we will wait and do another blood test in a few days.  At that time the inflammation markers had gone down.  My body had "done the job".

 

Another example.  I was diagnosed diabetic with high cholesterol in October 2021.  Doctor wanted to change diet (probably low FAT), start a statin (can increase risk/worsen diabetes) and also metformin (can increase obesity).  Three variables!  I said no and did my own research, thankfully finding out about low CARB diet.  After only 3 months my Hba1c is below 5.5 so my diabetes is in remission/reversed, my liver function tests are normal, my cholesterol has improved and my blood pressure reduced (I am only on a very low dose of perindopril now).  If I had taken the drugs and changed my diet to low carb I think that the drugs would have been "praised" as doing their job and I would have ended up on them long term with the side effects.

 

 

 

I saw a video just a couple of days ago.  I've highlighted the important parts in the transcript.  And I wonder why I am now cautiously cynical.

 

https://youtu.be/ladtvxTAYYw

 

from the transcript:

 

22:27
drug companies can distort the literature on statins so one of their favorite ways is to have what we call a
22:33
run-in period so i was just reading a study the other day on statins and what they did is that they gave
22:39
before the trials started they gave everybody a statin and 11 000 of them approximately had
22:46
significant side effects so they were withdrawn from the study before it even started
22:53
now do you think the side effect data was based on these 11 000 people who withdraw with side effects or do you
22:59
think it was based on the population that was remaining who had then proven
23:04
that they were tolerant to statins so this is abuse of a run-in period and there's multiple other ways that we can
23:10
actually get to the truth of it but in reality as you say peter it's at least one in four people have significant side
23:16
effects from statins

 

 

 

Please be aware that these videos might be triggering, so please make your own decision about whether you are in the right place mentally to listening to them.  For me, I find that knowledge is power.

 

Gwen Olsen was a pharmaceutical representative.  She has personal experience using psychiatric drugs as well as her niece.

 

Interview:  Confessions of an Rx Drug Pusher (51 minutes Gwen Olsen - ex pharmaceutical representative)
 

* NO LONGER ACTIVE on SA *

MISSION ACCOMPLISHED:  (6 year taper)      0mg Pristiq  on 13th November 2021

ADs since ~1992:  25+ years - 1 unknown, Prozac (muscle weakness), Zoloft; citalopram (pooped out) CTed (very sick for 2.5 wks a few months after); Pristiq:  50mg 2012, 100mg beg 2013 (Serotonin Toxicity)  Tapering from Oct 2015 - 13 Nov 2021   LAST DOSE 0.0025mg

Post 0 updates start here    My tapering program     My Intro (goes to tapering graph)

 VIDEO:   Antidepressant Withdrawal Syndrome and its Management

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18 hours ago, hugugh said:

antidepressants really are no better than placebo

 

The problem is not so much that ADs are no better than placebo as it is that ADs are decidedly worse than placebo in terms of the harm they can do. A placebo doesn't do harm

I was skeptical about psych drugs pretty much from the beginning, but being ignorant of the potential risks, I just figured:

What is there to lose? If they're no better than placebo, then why not try? If they don't work, I'll be no worse off than when I started. If they work from a placebo effect, at least they're working. If they work from the chemicals, at least they're working. 

That was my reasoning for years and years. Meanwhile I had no clue that they were actually actively doing harm. Had the risks been known to me I would have opted out.  

 

18 hours ago, hugugh said:

I don't understand how drugs with such terrible side effects and with very little/no efficacy were approved for use and became so popular throughout the world.  I am not a conspiracy theorist so I'm having a hard time wrapping my head around the idea that anti-depressants might just be one giant scam between pharmaceutical companies, regulatory agencies and doctors.  How is this possible?  If this research is real (and it sure looks convincing) and antidepressants really are no better than placebo, then if the research was not muddled and hidden, my poor daughter would have been saved from years of torment that almost took her life.  It makes me want to tear my hair out thinking about this.

 

I hear you, @hugugh. It is shocking, appalling, maddening, unfathomable, scandalous, outrageous, etc. The mind balks. 

I'm so sorry that you and your daughter have been affected by this. I'm so sorry that we have all been so negatively impacted by this and that things are so messed up in the world. 

 

It would be really cool if parents such as yourself came together to advocate for other families and children in activist efforts to stop the prescribing of psych drugs to children! 

Have you considered forms of activism on this issue? I ask not only because the world needs action but because one of the best remedies for torment and shock and rage and trauma is taking action. One day when you feel ready, you may consider getting involved hands on. There may already be initiatives out there or maybe you could start something.

Anything and everything counts. Not everyone can be Altostrata, but if nothing else, we can donate to SA to help keep this place going. 

 

16 hours ago, ChessieCat said:

What I would like to say is that at least you know now.  You did what you did at the time, with the knowledge you had at the time. 

 

  • You did what you did because you care about your daughter and thought you were doing the right thing
  • You have more information now
  • You now know how to find information before deciding on what action to take
  • You are now better able to make informed decisions
  • You are doing the best you can

 

This is something that I think a lot of us have trouble getting our heads around.  And I think that the anger we have about it is warranted. 

 

Well said, ChessieCat. 

 

Thanks for this topic, @hugugh

 

1996-2018 - misc. polypharmacy, incl. SSRIs, SNRIs, neuroleptics, lithium, benzos, stimulants, antihistamines, etc. (approx. 30+ drugs)

2012-2018 - 10mg lexapro/escitalopram (20mg?)    Jan. 2018 - 10mg -> 5mg, then from 5mg -> 2.5mg, then 0mg  -->  July 2018 - 0mg

2017(?)-2020 - vyvanse/lisdexamfetamine 60-70mg    2020-2021 - 70mg down to 0mg  -->  July 2021 - 0mg

March-April 2021 - vortioxetine 5-10mg (approx. 7 weeks total; CT)  -->  April 28th, 2021 - 0mg

supplements: magnesium powder (dissolved in water) as needed throughout the day; 1 tsp fish oil w/ morning meal; 2mg melatonin 

August 1, 2022 - 1 mg melatonin

 

Courage is fear that has said its prayers.  - Karle Wilson Baker

love and justice are not two. without inner change, there can be no outer change; without collective change, no change matters.  - Rev. angel Kyodo williams

Holding multiple truths. Knowing that everyone has their own accurate view of the way things are.  - text on homemade banner at Afiya house

 

I am not a medical professional; this is not medical advice. 

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On 6/9/2022 at 7:36 AM, hugugh said:

I've been slightly obsessed and majorly confused with this article since I found it:  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2253608/

 

I don't understand how drugs with such terrible side effects and with very little/no efficacy were approved for use and became so popular throughout the world.  I am not a conspiracy theorist so I'm having a hard time wrapping my head around the idea that anti-depressants might just be one giant scam between pharmaceutical companies, regulatory agencies and doctors.  How is this possible?  If this research is real (and it sure looks convincing) and antidepressants really are no better than placebo, then if the research was not muddled and hidden, my poor daughter would have been saved from years of torment that almost took her life.  It makes me want to tear my hair out thinking about this.

 

Has anyone seen this research?  Opinions? 

 

there's also plenty of research that shows anti-depressants are decent at doing what they're supposed to do, ie relieving symptoms of depression. 

 

I do not have a single doubt in my mind that ADs are better than placebo, and an AD saved my bacon when I needed it. Before trying it, I had tried half a dozen meds, none of which had worked. 

 

It's like everything: if you look for science studies aiming at disproving climate change, you'll find quite a few of them, all written in ways that sound and look convincing to someone who isn't a scientist. It doesn't make them right. 

 

Nov 2019: put on amitriptyline 100mg for insomnia. Worked great, sleep back to normal by March 2020

Jan 2020: Amitriptyline down to 50mg. Some withdrawal for two weeks.

April-May 2020: tapered off amitriptyline a first time over 6 weeks. withdrawal.

June 2020: reinstated amitriptyline 50mg a first time. Things improved progressively for 6 months. Backto normal in November

December 2020: new attempt at tapering amitriptyline (from 50mg), slower this time

February 2021: 30mg amitriptyline... withdrawal starts

March 2021: reinstatement 35mg amitriptyline, then 50mg late march.

April 2021: increased dosage to 75mg; Kindling started, HORRIFIC.

July 2021: reinstatement clearly made things worse so I decide to taper slowly again, at 2.5mg per month

March-April 2022: I hit 45mg amitriptyline dosage, withdrawal has drastically improved, symptom intensity down to 2 or 3 out of ten. Able to exercise, drink etc no issues. I pause the taper. I have stayed on 45mg of amitriptyline ever since.

May 2022: New wave of withdrawal, lasts until January 2023 (nerve pain in my skull)

May 2023: New wave, this time anxiety and pins and needles in my head, much like the kindling reaction in 2021. Not sure what caused it. Wave still ongoing.

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On 6/8/2022 at 4:36 PM, hugugh said:

I don't understand how drugs with such terrible side effects and with very little/no efficacy were approved for use and became so popular throughout the world. 

 

There is a vast amount of commentary on this, and the decline of the FDA and other regulatory agencies due to "regulatory capture" by the pharmaceutical industry. For what it's worth, European regulators tend to be a little more stringent. 

 

12 hours ago, HugHK said:

I do not have a single doubt in my mind that ADs are better than placebo, and an AD saved my bacon when I needed it. Before trying it, I had tried half a dozen meds, none of which had worked. 

 

That is just wonderful that the 7th drug you tried "worked". That is a success rate of 1/7, or about 14%. The estimated number needed to treat (NNT) for one person to benefit from antidepressant prescription is 7-9, meaning 6/7-8/9 people taking an antidepressant will see no benefit. (Some put the NNT for antidepressants to be an even more dismal 10-20.)

 

Among other drugs, these ratios are not considered to show a high rate of benefit or efficacy.

 

In addition, these drugs have drawbacks, which may be represented in NNH (number needed to harm). You are experiencing one of these yourself, in your own difficulty going off your miracle drug. Generally, regulators need to evaluate NNT with NNH, but both NNT and NNH have not been well studied with antidepressants. So your assertion "I do not have a single doubt" is based entirely on your own subjective belief, which may be a consolation for you now that you're paying the cost for your trust in the drugs.

This is not medical advice. Discuss any decisions about your medical care with a knowledgeable medical practitioner.

"It has become appallingly obvious that our technology has surpassed our humanity." -- Albert Einstein

All postings © copyrighted.

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4 hours ago, Altostrata said:

 

There is a vast amount of commentary on this, and the decline of the FDA and other regulatory agencies due to "regulatory capture" by the pharmaceutical industry. For what it's worth, European regulators tend to be a little more stringent. 

 

 

That is just wonderful that the 7th drug you tried "worked". That is a success rate of 1/7, or about 14%. The estimated number needed to treat (NNT) for one person to benefit from antidepressant prescription is 7-9, meaning 6/7-8/9 people taking an antidepressant will see no benefit. (Some put the NNT for antidepressants to be an even more dismal 10-20.)

 

Among other drugs, these ratios are not considered to show a high rate of benefit or efficacy.

 

In addition, these drugs have drawbacks, which may be represented in NNH (number needed to harm). You are experiencing one of these yourself, in your own difficulty going off your miracle drug. Generally, regulators need to evaluate NNT with NNH, but both NNT and NNH have not been well studied with antidepressants. So your assertion "I do not have a single doubt" is based entirely on your own subjective belief, which may be a consolation for you now that you're paying the cost for your trust in the drugs.

you're right that other meds didn't work (although they included only two other ADs, as well as benzos, anti-psychotics and Lyrica for eg). 

 

But at the tend of the day, I did find one that works, whereas any 'natural' method gave me 0% relief... So as far as I am concerned, the AD I take got me out of the hole I was in back in 2019. (and put me back in another hole when doctors wrongly advised me on how to come off, but that's a different story). 

Nov 2019: put on amitriptyline 100mg for insomnia. Worked great, sleep back to normal by March 2020

Jan 2020: Amitriptyline down to 50mg. Some withdrawal for two weeks.

April-May 2020: tapered off amitriptyline a first time over 6 weeks. withdrawal.

June 2020: reinstated amitriptyline 50mg a first time. Things improved progressively for 6 months. Backto normal in November

December 2020: new attempt at tapering amitriptyline (from 50mg), slower this time

February 2021: 30mg amitriptyline... withdrawal starts

March 2021: reinstatement 35mg amitriptyline, then 50mg late march.

April 2021: increased dosage to 75mg; Kindling started, HORRIFIC.

July 2021: reinstatement clearly made things worse so I decide to taper slowly again, at 2.5mg per month

March-April 2022: I hit 45mg amitriptyline dosage, withdrawal has drastically improved, symptom intensity down to 2 or 3 out of ten. Able to exercise, drink etc no issues. I pause the taper. I have stayed on 45mg of amitriptyline ever since.

May 2022: New wave of withdrawal, lasts until January 2023 (nerve pain in my skull)

May 2023: New wave, this time anxiety and pins and needles in my head, much like the kindling reaction in 2021. Not sure what caused it. Wave still ongoing.

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You'll have to allow that such difficulties do, indeed, cause other people to have more than a single doubt that taking an antidepressant would be a good idea for them.

This is not medical advice. Discuss any decisions about your medical care with a knowledgeable medical practitioner.

"It has become appallingly obvious that our technology has surpassed our humanity." -- Albert Einstein

All postings © copyrighted.

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35 minutes ago, Altostrata said:

You'll have to allow that such difficulties do, indeed, cause other people to have more than a single doubt that taking an antidepressant would be a good idea for them.

 

Yeah I fully agree with that, but I feel like I take a more nuanced approach when it comes to why they are prescribed at all. for ADs to help some people is already better than not having them 9as far as I'm concerned. 

 

to be clear I' m not trying to anger anyone and I know my views don't reflect the consensus on the forum, but I do think it's important to try to look beyond personal experience and look at the wider benefits. 

Nov 2019: put on amitriptyline 100mg for insomnia. Worked great, sleep back to normal by March 2020

Jan 2020: Amitriptyline down to 50mg. Some withdrawal for two weeks.

April-May 2020: tapered off amitriptyline a first time over 6 weeks. withdrawal.

June 2020: reinstated amitriptyline 50mg a first time. Things improved progressively for 6 months. Backto normal in November

December 2020: new attempt at tapering amitriptyline (from 50mg), slower this time

February 2021: 30mg amitriptyline... withdrawal starts

March 2021: reinstatement 35mg amitriptyline, then 50mg late march.

April 2021: increased dosage to 75mg; Kindling started, HORRIFIC.

July 2021: reinstatement clearly made things worse so I decide to taper slowly again, at 2.5mg per month

March-April 2022: I hit 45mg amitriptyline dosage, withdrawal has drastically improved, symptom intensity down to 2 or 3 out of ten. Able to exercise, drink etc no issues. I pause the taper. I have stayed on 45mg of amitriptyline ever since.

May 2022: New wave of withdrawal, lasts until January 2023 (nerve pain in my skull)

May 2023: New wave, this time anxiety and pins and needles in my head, much like the kindling reaction in 2021. Not sure what caused it. Wave still ongoing.

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On 6/9/2022 at 9:36 AM, hugugh said:

 

The study got me thinking.  Under the subtitle "What do these findings mean?" : 

 

"These findings suggest that, compared with placebo, the new-generation antidepressants do not produce clinically significant improvements in depression in patients who initially have moderate or even very severe depression, but show significant effects only in the most severely depressed patients."  

I wonder if this is based on the prognosis for the most severe depression.  AD's can cause suicide (according to the black box warning on the labels).  I did not read the whole article, but I tried using Ctrl + F for the word "suicide" and nothing came up.

 

"The findings also show that the effect for these patients seems to be due to decreased responsiveness to placebo, rather than increased responsiveness to medication...In addition, the finding that extremely depressed patients are less responsive to placebo than less severely depressed patients but have similar responses to antidepressants is a potentially important insight into how patients with depression respond to antidepressants and placebos that should be investigated further." 

 

In the further investigation proposed here, maybe they should look into a special type of placebo that creates side effects (perhaps headaches, dehydration, etc.), so that the patient is convinced s/he is consuming a drug.  If I remember correctly, D. Healy mentions this type of placebo in Pharmageddon.  (I don't have the book on hand.)

 

"Given these results, the researchers conclude that there is little reason to prescribe new-generation antidepressant medications to any but the most severely depressed patients unless alternative treatments have been ineffective." 

 

This is in line with my opinion.  Alternatives should be more readily available and tried with persistence first.  Also, in my opinion, the drug should be used for the shortest possible duration of time. 

 

Edited by ChessieCat
unbolded

My psychiatric drug history goes back, on and off, to 1999.  This is my taper chronology:

Jan. 2018:                        900 mg  Lithium                      1 mg Risperidone               250 mg Lamotrigine 

Jan. 2018:                        0 mg  Lithium*                        1 mg Risperidone               250 mg Lamotrigine 

Jan. 2019:                        0 mg Lithium                           0.625 mg Risperidone       175 mg Lamotrigine

Jan. 2020:                       0 mg Lithium                           0.260 mg Risperidone       175 mg Lamotrigine

Feb. 2021:                        0 mg Lithium                           0 mg Risperidone              175 mg Lamotrigine

August 2021                    0 mg Lithium                           0 mg Risperidone              0 mg Lamotrigine

*I had to cold turkey lithium because of life-threatening side effects.

Measuring doses: The Withdrawal Project at the Inner Compass Initiative website, which explains how to do the microtaper to make it as smooth as possible   Nutrition: The Clean Gut Diet by Alejandro Junger, MD, and Viva Naturals Omega 3 Fish Oil Supplements.  Psychological: "Dr. Bruce H. Lipton Explains How To Reprogram The Subconscious Mind" (on YouTube) and PSYCH-K (an alternative healing modality).  

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To clarify what I am trying to say :

 

The outcomes for the most severely depressed patients looked better.  However, it is still possible based on what is known about ADs causing suicide, that if there were any deaths among the study participants, then the ADs could have been responsible.

 

 

Edited by ChessieCat
extracted post from quote

My psychiatric drug history goes back, on and off, to 1999.  This is my taper chronology:

Jan. 2018:                        900 mg  Lithium                      1 mg Risperidone               250 mg Lamotrigine 

Jan. 2018:                        0 mg  Lithium*                        1 mg Risperidone               250 mg Lamotrigine 

Jan. 2019:                        0 mg Lithium                           0.625 mg Risperidone       175 mg Lamotrigine

Jan. 2020:                       0 mg Lithium                           0.260 mg Risperidone       175 mg Lamotrigine

Feb. 2021:                        0 mg Lithium                           0 mg Risperidone              175 mg Lamotrigine

August 2021                    0 mg Lithium                           0 mg Risperidone              0 mg Lamotrigine

*I had to cold turkey lithium because of life-threatening side effects.

Measuring doses: The Withdrawal Project at the Inner Compass Initiative website, which explains how to do the microtaper to make it as smooth as possible   Nutrition: The Clean Gut Diet by Alejandro Junger, MD, and Viva Naturals Omega 3 Fish Oil Supplements.  Psychological: "Dr. Bruce H. Lipton Explains How To Reprogram The Subconscious Mind" (on YouTube) and PSYCH-K (an alternative healing modality).  

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On 6/11/2022 at 1:20 PM, carefulprayerful said:

Also, in my opinion, the drug should be used for the shortest possible duration of time. 

My daughter's doctor told me she should be on Zoloft for the rest of her life - she was 10 years old.  No psychiatrist ever suggested that she tried life without medications once she started - they just kept adding more and more meds.  It seems criminal to tell an 11 year old they should be on a prescription drug the rest of her life for what apparently was a temporary issue she had at age 10. 

Daughter's Med History: 

Zoloft (25 mg-200mg) 2019-2022.  Cold turkeyed April 2022

Guanfacine (1mg-4mg) 2021-2022.  Tapered off May 2022

Lamictal (low dose) 2021 for brief period

Abilify (can't remember dose) 2021-2022 

Seroquel 2022 (225 mg):  Cold turkeyed April 2022

Naltrexone 2022 (brief period -stopped cold turkey)

Lexapro (5mg) 2022:  Started to help with withdrawal symptoms.  Only on for 2 weeks. 

Med free as of May 2022

 

 

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2 minutes ago, hugugh said:

My daughter's doctor told me she should be on Zoloft for the rest of her life - she was 10 years old.  No psychiatrist ever suggested that she tried life without medications once she started - they just kept adding more and more meds.  It seems criminal to tell an 11 year old they should be on a prescription drug the rest of her life for what apparently was a temporary issue she had at age 10. 

 

@hugugh I'm so sorry. This is truly awful and stupid and wrong. Unfortunately it's not surprising. 

Good on you for high-tailing it outta there! Your daughter is lucky to have you <3 

 

1996-2018 - misc. polypharmacy, incl. SSRIs, SNRIs, neuroleptics, lithium, benzos, stimulants, antihistamines, etc. (approx. 30+ drugs)

2012-2018 - 10mg lexapro/escitalopram (20mg?)    Jan. 2018 - 10mg -> 5mg, then from 5mg -> 2.5mg, then 0mg  -->  July 2018 - 0mg

2017(?)-2020 - vyvanse/lisdexamfetamine 60-70mg    2020-2021 - 70mg down to 0mg  -->  July 2021 - 0mg

March-April 2021 - vortioxetine 5-10mg (approx. 7 weeks total; CT)  -->  April 28th, 2021 - 0mg

supplements: magnesium powder (dissolved in water) as needed throughout the day; 1 tsp fish oil w/ morning meal; 2mg melatonin 

August 1, 2022 - 1 mg melatonin

 

Courage is fear that has said its prayers.  - Karle Wilson Baker

love and justice are not two. without inner change, there can be no outer change; without collective change, no change matters.  - Rev. angel Kyodo williams

Holding multiple truths. Knowing that everyone has their own accurate view of the way things are.  - text on homemade banner at Afiya house

 

I am not a medical professional; this is not medical advice. 

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  • 1 month later...
  • Moderator
On 6/8/2022 at 7:36 PM, hugugh said:

I've been slightly obsessed and majorly confused with this article since I found it:  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2253608/

 

I don't understand how drugs with such terrible side effects and with very little/no efficacy were approved for use and became so popular throughout the world.  I am not a conspiracy theorist so I'm having a hard time wrapping my head around the idea that anti-depressants might just be one giant scam between pharmaceutical companies, regulatory agencies and doctors.  How is this possible?  If this research is real (and it sure looks convincing) and antidepressants really are no better than placebo, then if the research was not muddled and hidden, my poor daughter would have been saved from years of torment that almost took her life.  It makes me want to tear my hair out thinking about this.

 

Has anyone seen this research?  Opinions? 

@hugughthat article is legit and there are many like it out there. 

Here Prof Kirsch explains his findings in a less academic way. And his journey to these findings. 
Antidepressants and the Placebo Effect - PMC (nih.gov)

"Nothing so small as a moment is insurmountable, and moments are all that we have. You have survived every trial and tribulation that life has thrown at you up until this very instant. When future troubles come—and they will come—a version of you will be born into that moment that can conquer them, too." - Kevin Koenig 

 

I am not a doctor and this should not be considered medical advice. You can use the information and recommendations provided in whatever way you want and all decisions on your treatment are yours. 

 

In the next few weeks I do not have a lot of capacity to respond to questions. If you need a quick answer pls tag or ask other moderators who may want to be tagged. 

 

Aug  2000 - July 2003 (ct, 4-6 wk wd) , citalopram 20 mg,  xanax prn, wellbutrin for a few months, trazodone prn 

Dec 2004 - July 2018 citalopram 20 mg, xanax prn (rarely used)

Aug 2018 - citalopram 40 mg (self titrated up)

September 2018 - January 2019 tapered citalopram - 40/30/20/10/5 no issues until a week after reaching 0

Feb 2019 0.25 xanax - 0.5/day (3 weeks) over to klonopin 0.25 once a day to manage severe wd

March 6, reinstated citalopram 2.5 mg (liquid), klonopin 0.25 mg for sleep 2-3 times a week

Apr 1st citalopram 2.0 mg (liquid), klonopin 0.25 once a week (off by 4/14/19- no tapering)

citalopram (liquid) 4/14/19 -1.8 mg, 5/8/19 - 1.6 mg,  7/27/19 -1.5 mg,  8/15/19 - 1.35, 2/21/21 - 1.1 (smaller drops in between), 6/20/21 - 1.03 mg, 8/7/21- 1.025, 8/11/21 - 1.02, 8/15/21 - 1.015, 9/3/21 - 0.925 (fingers crossed!), 10/8/21 - 0.9, 10/18/21 - 0.875, 12/31/21 - 0.85, 1/7/22 - 0.825, 1/14/22 - 0.8, 1/22/22 - 0.785, 8/18/22 - 0.59, 12/15/2022 - 0.48, 2/15/22 - 0.43, 25/07/23 - 0.25 (mistake), 6/08/23 - 0.33mg

 

Supplements: magnesium citrate and bi-glycinate

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  • Moderator Emeritus

@hugugh

 

Here's a video about the same thing which I found easier to understand.  Prof Kirsch and his cohorts used Freedom of Information to get the unpublished clinical trials. 

 

Excerpt from the paper that Onmyway linked above:

How Did These Drugs Get Approved?
....
The FDA requires two adequately conducted clinical trials showing a significant difference between drug and placebo.  But there is a loophole:  there is no limit to the number of trials that can be conducted in search of these two significant trials.  Trials showing negative results simply do not count.  Furthermore, the clinical significance of the findings is not considered.  All that matters is that the results are statistically significant.
....
(NB:  emphasis in abstract and excerpt are mine)

* NO LONGER ACTIVE on SA *

MISSION ACCOMPLISHED:  (6 year taper)      0mg Pristiq  on 13th November 2021

ADs since ~1992:  25+ years - 1 unknown, Prozac (muscle weakness), Zoloft; citalopram (pooped out) CTed (very sick for 2.5 wks a few months after); Pristiq:  50mg 2012, 100mg beg 2013 (Serotonin Toxicity)  Tapering from Oct 2015 - 13 Nov 2021   LAST DOSE 0.0025mg

Post 0 updates start here    My tapering program     My Intro (goes to tapering graph)

 VIDEO:   Antidepressant Withdrawal Syndrome and its Management

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