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Bupe Suboxone/Buprenorphine FAQ & Megathread v2; 2010

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this isn't like shock therapy is it? i know they use shock therapy to help//cure depression and it does infact work, i've seen it. if shock therapy could cure my addiction to opiates, i'd be in the hospital right now hooked up to the machine!

if this has been around since the 80's and there are people who have benefited from it, why is it not more popular or more heard of? it truly seems like there are so many treatment options//therapies for all kinds of things that just get pushed aside for whatever reasons.

I doubt you have "seen it work", nor would you so willingly hook yourself up to the machine.

Effects on memory

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It is the puported effects of ECT on long-term memory that give rise to much of the concern surrounding its use.[26] The acute effects of ECT can include amnesia, both retrograde (for events occurring before the treatment) and anterograde (for events occurring after the treatment).[27] However, the vast majority of these effects are short lived. Memory loss and confusion are more pronounced with bilateral electrode placement rather than unilateral, and with outdated sine-wave rather than brief-pulse currents. The vast majority of modern treatment uses brief pulse currents.[27] Research by Harold Sackeim has shown that excessive current causes more risk for memory loss, and using right-sided electrode placement may reduce verbal memory disturbance.[28]

Retrograde amnesia is most marked for events occurring in the weeks or months before treatment, with one study showing that although some people lose memories from years prior to treatment, recovery of such memories was "virtually complete" by seven months post-treatment, with the only enduring loss being memories in the weeks and months prior to the treatment.[29][30] Anterograde memory loss is usually limited to the time of treatment itself or shortly afterwards. In the weeks and months following ECT these memory problems gradually improve, but some people have persistent losses, especially with bilateral ECT.[12][27] One published review summarizing the results of questionnaires about subjective memory loss found that between 29% and 55% of respondents believed they experienced long-lasting or permanent memory changes.[31] In 2000, American psychiatrist Sarah Lisanby and colleagues found that bilateral ECT left patients with more persistently impaired memory of public events as compared to RUL ECT.[26]

Some studies have found that patients are often unaware of cognitive deficits induced by ECT.[32][33] For example, in June 2008, a Duke University study[32] was published assessing the neuropsychological effects and attitudes in patients after ECT. Forty-six patients participated in the study, which involved neuropsychological and psychological testing before and after ECT. The study documented substantial cognitive impairment after ECT on a variety of memory tests, including "verbal memory for word lists and prose passages and visual memory of geometric designs." The study further found that a significant number of patients believed that their memory had improved after ECT despite the fact that neuropsychological testing clearly showed the opposite. As stated by the researchers, "Indeed, there was a slight trend towards [patients reporting] improved memory functioning, despite the objective neuropsychological data indicating significantly lower recognition and delayed recall." Based on their findings, the authors issued the following recommendation:

"When ECT is provided to adolescents, the potential impact of such cognitive changes should be discussed with the patients and their parents or guardians in terms of implications for not only the patient’s emotional functioning but cognitive functioning as well, particularly upon his or her academic performance. In summary, we argue that an individual cost-benefit analysis should be made in light of the implications of the potential benefits versus costs of ECT upon improving emotional functioning and the impact that potential memory changes may have on real-world functioning and quality of life."[32]

Severe memory loss from ECT is described in an autobiographical book by Linda Andre[34].


Controversy over long-term effects on general cognition
NSFW:
According to prominent ECT researcher Harold Sackeim, "despite over fifty years of clinical use and ongoing controversy", until 2007 there had "never been a large-scale, prospective study of the cognitive effects of ECT."[35] In this first-ever large-scale study (347 subjects), Sackeim and colleagues found that at least some forms (namely bilateral application and outdated sine-wave currents) of ECT "routine[ly]" lead to "adverse cognitive effects," including global cognitive deficits and memory loss, that persist for up to six months after treatment, suggesting that the induced deficits may be permanent.[35][36] The authors also warned that their findings did not suggest that right-unilateral ECT did not also lead to chronic cognitive deficits. However, the several limitations of this study include the lack of a depressed control group with which to compare memory decay over 6 months. The measure of autobiographical memory used, the Columbia Autobiographical Short-Form (AMI-SF) is not capable of showing memory improvement, with scores at followup expressed as percentages of baseline.

Harold Sackeim can be seen in a videotaped deposition briefly discussing the findings of this study and why, in his opinion, earlier studies had failed to find evidence of long-term harm from ECT.[37] Despite over fifty years of clinical use, Sackeim states that prior to 2001, "the field itself never really had an opportunity to have a discussion about patients who have complaints about long-term memory loss." In this video clip, Sackeim also reveals that at a California ECT conference with 200 practitioners present, when polled as to whether they think ECT can lead to chronic cognitive deficits, two-thirds raised their hands. Sackeim says this was "almost a watershed moment for the field", and was the "first time publicly that the field itself said 'no' to the position that it can't happen."[37][38]

In July 2007, a second study was published concluding that ECT routinely leads to chronic, substantial cognitive deficits, and the findings were not limited to any particular forms of ECT.[39] The study, led by psychiatrist Glenda MacQueen and colleagues, found that patients treated with ECT for bipolar disorder show marked deficits across multiple cognitive domains. According to the researchers, "Subjects who had received remote ECT had further impairment on a variety of learning and memory tests when compared with patients with no past ECT. This degree of impairment could not be accounted for by illness state at the time of assessment or by differential past illness burden between patient groups." Despite the findings of chronic, global cognitive deficits in post-ECT patients, MacQueen and colleagues suggest that it is "unlikely that such findings, even if confirmed, would significantly change the risk–benefit ratio of this notably effective treatment."[39]

Six months after the publication of the Sackeim study[35] documenting routine, long-term memory loss after ECT, prominent ECT researcher Max Fink published a review in the journal Psychosomatics concluding that patient complaints of memory loss after ECT are "rare" and should be "characterized as somatoform disorders, rather than as evidence of brain damage, thus warranting psychological treatment for such disorders."[40] Based on his findings, Fink suggests that, "Instead of endorsing these reports as the direct consequence of ECT, especially in patients who have recovered from their depressive illness, lost their suicidal drive, and have improved social functioning, is it not more useful to accept the complaint as a somatoform disorder, explore the basis in the individual’s history and experience, and offer appropriate supportive treatment?"[40]

Most recent reviews of the literature and other articles continue to characterize ECT as safe and effective.[41][42][43][44][45][46][47][48] For example, in June 2009, Portuguese researchers published a review on the safety and efficacy of ECT in an article entitled, Electroconvulsive Therapy: Myths and Evidences.[41] In their review, the researchers conclude that ECT is an "efficient, safe and even life saving treatment for several psychiatric disorders." In 2008, Yale researchers published a review on the safety and efficacy of ECT in elderly patients.[48] According to the authors, "ECT is well established as a safe and effective treatment for several psychiatric disorders." And in a June 2009 article published in the Journal of ECT, Iranian researchers observe that, "Despite the wide consensus over the safety and efficacy of electroconvulsive therapy (ECT), it still faces negative publicity and unfavorable attitudes of patients and families."[47]

Psychiatrist Peter Breggin, chief editor of the journal Ethical Human Psychology and Psychiatry, is a leading critic of ECT who believes the procedure is neither safe nor effective. In a published article reviewing the findings of Harold Sackeim's 2007 study[35] on the cognitive effects of ECT, Breggin accuses Max Fink and other pro-ECT researchers of having a history of "systematically covering up damage done to millions of [ECT] patients throughout the world."[36] He disagrees with the position that findings of chronic, global cognitive deficits should have no bearing on the risk-benefit ratio of ECT, and he believes it's important to address the "actual impact of these losses on the lives of individual patients." In a section of his paper entitled Destroying Lives, Dr. Breggin writes, "Even when these injured people can continue to function on a superficial social basis, they nonetheless suffer devastation of their identities due to the obliteration of key aspects of their personal lives. The loss of the ability to retain and learn new material is not only humiliating and depressing but also disabling. Even when relatively subtle, these activities can disrupt routine activities of living."[36]

A study published in 2004 in the Journal of Mental Health reported that 35 to 42% of patients responding to a questionnaire reported ECT resulted in loss of intelligence.[49] The study also reported, "There is no overlap between clinical and consumer studies on the question of benefit."

A recent opinion article by a neuropsychologist and a psychiatrist in Dublin suggests that ECT patients who experience cognitive problems following ECT should be offered some form of cognitive rehabilitation. The authors say that the failure to attempt to rehabilitate patients may be partly responsible for the negative public image of ECT. The article speculates on what aspects of such rehabilitation might be useful, without reviewing the literature on its presence or absence. [50]


Effects on brain structure
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Considerable controversy exists over the effects of ECT on brain tissue despite the fact that a number of mental health associations, including the American Psychiatric Association, have concluded that there is no evidence that ECT causes structural brain damage.[9][25][51] A 1999 report by the United States Surgeon General states, "The fears that ECT causes gross structural brain pathology have not been supported by decades of methodologically sound research in both humans and animals".[5] However, not all experts agree that ECT does not cause brain damage, and two studies have been published since 2007 finding that at least some forms of ECT may result in widespread, persisting, generalized cognitive dysfunction, which might support claims that ECT causes brain damage.[35][39][52]

A leading critic of ECT, psychiatrist Peter Breggin has published books and journalistic reviews of the literature purporting to show that ECT routinely causes brain damage as evidenced by a considerable list of studies in humans and animals.[53] In particular, Dr. Breggin asserts that animal and human autopsy studies have shown that ECT routinely causes ‘widespread pinpoint hemorrhages and scattered cell death.’[52] According to Dr. Breggin, the 1990 APA task force report on ECT ignored much of the scientific literature pointing out the negative effects of electroshock therapy. For example, in 1952 Hans Hartelius conducted and published an animal study on cats entitled Cerebral Changes Following Electrically Induced Convulsions in which a double-blind microscopic pathology examination showed that it was possible to distinguish the 8 shocked animals from the 8 non-shocked animals with remarkable accuracy based on statistically significant structural changes to the brain, including vessel wall changes, gliosis, and nerve cell changes. Based on the detection of shadow cells and neuronophagia, Hartelius determined that there was irreversible damage to neurons associated with electroshock.[52]

Proponents argue that the addition of hyperoxygenation and refinement in technique in the last thirty years has made ECT safe, and a majority of published reviews in recent decades have reflected this position.[54] In a 2004 study designed to evaluate whether modern ECT techniques lead to identifiable brain damage, twelve monkeys underwent daily electroshock for six weeks under conditions meant to simulate human ECT; the animals were then sacrificed and their brains were compared to monkeys undergoing anesthesia alone. According to the researchers, "None of the ECT-treated monkeys showed pathological findings."[55]

There are recent animal studies that have documented significant brain damage after an electroshock series. For example, in 2005, Russian researchers published a study entitled, Electroconvulsive Shock Induces Neuron Death in the Mouse Hippocampus: Correlation of Neurodegeneration with Convulsive Activity. In this study, the researchers found that after an electroshock series, there was a significant loss of neurons in parts of the brain and particularly in defined parts of the hippocampus where up to 10% of neurons were killed. The researchers conclude that "the main cause of neuron death is convulsions evoked by electric shocks."[56] In 2008, Portuguese researchers conducted a rat study aimed at answering the question of whether an electroshock series causes structural changes in vulnerable parts of the brain.[57] According to the authors, "This study answers positively the question of whether repeated administration of ECS seizures can cause brain lesions. Our data are consistent with findings from other animal models and from human studies in showing that neurons located in the entorhinal cortex and in the hilus of the dentate gyrus are particularly vulnerable to repeated seizures." However, they question the applicability of their own research with respect to Electroconvulsive therapy in humans: "An important caveat of our results is that it is unclear to what extent they are relevant to the use of electroconvulsive therapy in psychiatry, because the protocol employed in this study is different from that used clinically. Evidence from previous studies (Gombos et al., [1999]; Vaidya et al., [1999]) and from our pilot experiments indicates that treating rats either with five to ten widely spaced ECS (at 24- or 48-hr schedules) or with two stimulations only 2 hr apart does not lead to loss of hippocampal neurons".[58]

Many expert proponents of ECT maintain that the procedure is safe and does not cause brain damage. Dr. Charles Kellner, a prominent ECT researcher and former chief editor of the Journal of ECT states in a recent published interview that, "There are a number of well-designed studies that show ECT does not cause brain damage and numerous reports of patients who have received a large number of treatments over their lifetime and have suffered no significant problems due to ECT."[59] Dr. Kellner cites specifically to a study purporting to show an absence of cognitive impairment in eight subjects after more than 100 lifetime ECT treatments.[60] One of the authors of the cited study, Harold Sackeim, published a large-scale study less than a month after this interview concluding that the type of ECT used in the eight patients receiving the 100 lifetime treatments, bilateral sine wave, routinely leads to persistent, global cognitive deficits[35] (discussed supra). Dr. Kellner states that, "Rather than cause brain damage, there is evidence that ECT may reverse some of the damaging effects of serious psychiatric illness."[59]


Variations in international practice
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There is wide variation in ECT use between different countries, different hospitals, and different psychiatrists.[12] International practice varies considerably from widespread use of the therapy in many western countries to a small minority of countries that do not use ECT at all, such as Slovenia.[71] Guidelines on the use of ECT are stringent in the USA and the UK. Modern standards are not always followed throughout the world and not all countries that use ECT have written technical standards. The use of both anesthesia and muscle relaxants is universally recommended in the administration of ECT. If anesthesia and muscle relaxants are not used the procedure is called unmodified ECT. In a minority of countries such as Japan,[72] India,[73] and Nigeria,[74] ECT may be used without anesthesia. WHO has called for a worldwide ban on unmodified ECT and the topic is currently being debated in countries like India. The practice has been recently abolished in Turkey's largest psychiatric hospital.[75] A major difficulty for developing countries in eliminating unmodified ECT is a lack of trained anesthesiologists available to administer the procedure.[76] A small minority of countries never seek consent before administering ECT. This significantly uneven application of ECT around the world continues to make ECT a controversial procedure.

Sarah Hall reports, "ECT has been dogged by conflict between psychiatrists who swear by it, and some patients and families of patients who say that their lives have been ruined by it. It is controversial in some European countries such as the Netherlands and Italy, where its use is severely restricted".[77]


Mechanism of Action

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The aim of ECT is to induce a therapeutic clonic seizure (a seizure where the person loses consciousness and has convulsions) lasting for at least 15 seconds. Although a large amount of research has been carried out, the exact mechanism of action of ECT remains elusive. The main reasons for this are that the human brain can not be studied directly before and after ECT and therefore scientists rely on animal models of depression and ECT, with major limitations. While animal models are acknowledged to model merely aspects of depressive illness, human and animal brains are very similar at a molecular level, enabling detailed study of the molecular mechanisms involved in ECT[12]

There is a vast literature on the effects of Electroconvulsive Shock (ECS) in animals. In animal models of depression, particularly "Learned helplessness" and "Social defeat", there is evidence of pruning of normally dense synaptic connections in the hippocampus, a richly connected area deep in the temporal lobe which is vital in controlling both mood and memory.[90] ECS has been shown to increase levels of Brain-derived neurotrophic factor (BDNF) and Vascular Endothelial Growth Factor (VEGF) in the rodent hippocampus.[91] This reverses the toxic effects of depression on this area of the brain, increasing both new synapse formation and the formation of new brain cells (hippocampal neurogenesis). Both these effects have been noted to be present in antidepressant-treated animals, however they are neither necessary nor sufficient for antidepressant response. ECT is a more robust inducer of these neuroplastic effects than antidepressants. [92] Electroconvulsive Therapy (ECT) has also been shown to increase serum brain-derived neurotrophic factor (BDNF) in drug resistant depressed patients.[93] This suggests a commmon molecular mechanism of action, albeit in need of much further study.


Do you want to know how they tested learned helplessness in animals? They confined dogs to cages, and shocked them in their paws, repeatedly, until they stopped caring to jump/react. Yes, I know they did this, I studied about it in college, and the results were very clear that after a certain number of trials, all animals would stop flinching and have an environmentally induced state of "depression" or "learned helplessness".

There's absolutely no difference between this, and ECT in humans.

What stigup is talking about isn't ECT from what I am aware, and I am sorry to go this far off-topic, but I think it's important for most people to realize that most people should not endure ECT.

It's more humane to let someone slit their wrists and bleed to death than to put them through ECT.

Involuntary Experience of ECT in the United States


NSFW:
In most states in the USA, a judicial order following a formal hearing is needed before a patient can be forced to undergo involuntary ECT. Patients may be represented by legal counsel at the hearing. Oregon Revised Statutes allow for involuntary ECT with the signature of a physician independent of the patient's facility, and no judicial order or legal counsel are required. According to the Surgeon General's Report on Mental Health, "As a rule, the law requires that such petitions are granted only where the prompt institution of ECT is regarded as potentially lifesaving, as in the case of a person in grave danger because of lack of food or fluid intake caused by catatonia."[15] However, there are legal loopholes that thwart strict adherence to this principle. For example, an American citizen was being forced to undergo ECT against his will in 2009, even though his life was not in danger.[100][101] In this March 17, 2009 video, the man, his mother, and advocates, speak out against his forced ECT. The description of the video states that "Though Sandford, 54, is not charged with any crime, he has received over 40 such rounds of shocks on an outpatient basis so far – even after his original mental problems have long since subsided and he has repeatedly asked for the shocks to stop. Over the objections of Sandford, his mother and friends, his legal conservator at Lutheran Social Service of MN (LSSMN) has gone to court and succeeded in mandating a continuation of the procedure." Twin Cities Indymedia asserts "Like all other USA states, Minnesota has [legal] loopholes allowing [its] citizens to receive electroshock over their expressed wishes."[102]


Negative depictions of ECT

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Negative effects of ECT have been reported by noteworthy individuals.

Ernest Hemingway, American author, committed suicide shortly after ECT at the Menninger Clinic in 1961. He is reported to have said to his biographer, "Well, what is the sense of ruining my head and erasing my memory, which is my capital, and putting me out of business? It was a brilliant cure but we lost the patient...."[120]

In 2005, "Peggy S. Salters, 60, sued Palmetto Baptist Medical Center in Columbia, as well as the three doctors responsible for her care. As the result of an intensive course of outpatient ECT in 2000, she lost all memories of the past 30 years of her life, including all memories of her husband of three decades, now deceased, and the births of her three children. Ms. Salters held a Masters of Science in nursing and had a long career as a psychiatric nurse, but lost her knowledge of nursing skills and was unable to return to work after ECT."[121] The jury awarded Salters $635,177 in compensation for her inability to work. The judgement was upheld upon appeal.[122]

Registered nurse Barbara C. Cody reports in a letter to the Washington Post that her life was forever changed by 13 outpatient ECTs she received in 1983. "Shock 'therapy' totally and permanently disabled me. EEGs [electroencephalograms] verify the extensive damage shock did to my brain. Fifteen to 20 years of my life were simply erased; only small bits and pieces have returned. I was also left with short-term memory impairment and serious cognitive deficits. [deletion] Shock 'therapy' took my past, my college education, my musical abilities, even the knowledge that my children were, in fact, my children. I call ECT a rape of the soul."[123]

In 2007, a judge canceled a two year old court order that allowed the involuntary electroshock of Simone D., a psychiatric patient at Creedmoor Psychiatric Center in the state of New York.[124] Although Simone spoke only Spanish, she rarely received access to staff fluent in her language.[124][125] Simone previously had 200 electroshocks.[124][125] However, she communicated that she did not want more electroshock.[124][125] Simone stated, "Electroshock causes more pain. I suffer more from shock treatment![124] "

In 2008, David Tarloff, a psychiatric patient who had received electroshock, assaulted two therapists in the city of New York. Tarloff injured one therapist and killed the other. One of the therapists was Kent Shinbach, a psychiatrist who had an interest in electroconvulsive therapy. "It is not clear whether Dr. Shinbach played any role in Mr. Tarloff's shock therapy".[126] However, Tarloff told investigators that Shinbach had given Tarloff psychiatric treatment at a psychiatric facility initially in 1991.[127]

In an interview with Houston Chronicle in 1996, Melissa Holliday, a former extra on Baywatch and model for Playboy stated the ECT she received in 1995, "ruined her life." She went on to state, "I've been through a rape, and electroshock therapy is worse. If you haven't gone through it, I can't explain it."[128]

Liz Spikol, the senior contributing editor of Philadelphia Weekly, wrote of her ECT in 1996, "Not only was the ECT ineffective, it was incredibly damaging to my cognitive functioning and memory. But sometimes it's hard to be sure of yourself when everyone "credible"—scientists, ECT docs, researchers—are telling you that your reality isn't real. How many times have I been told my memory loss wasn't due to ECT but to depression? How many times have I been told that, like a lot of other consumers, I must be perceiving this incorrectly? How many times have people told me that my feelings of trauma related to the ECT are misplaced and unusual? It's as if I was raped and people kept telling me not to be upset—that it wasn't that bad."[129]
 
^ Jesus fucking christ, that is some fucked up shit - erasing 30 years of your life, what you learned in college etc. - and receving only $635,177 compensation... man that's fucked up that's like $20,000 a year. Sheeeiiiiiiiiiit.
 
^ Jesus fucking christ, that is some fucked up shit - erasing 30 years of your life, what you learned in college etc. - and receving only $635,177 compensation... man that's fucked up that's like $20,000 a year. Sheeeiiiiiiiiiit.

Exactly, I wanted you all to see that.

The human mind is a precious thing and people don't understand quite how permanent the damage from ECT is.

I have not read a lot about ECT, but my understanding of it is that immediately afterward, you are going to have to re-learn how to live your life. It isn't uncommon to forget how to use the bathroom, how to feed/clothe yourself, how to talk/communicate.

The way you process/form memories is going to be forever altered. The only way this would be a "good thing" is if you were a violent sociopath and society wanted some way of recovering the body for a different soul, so to speak.
 
I'm just curious as to why you think it wouldn't carry over well to humans?

Mice don't knowledgeably become heroin addicts, nor do they have a perception about what that is.

Human beings do. That means, human beings are still going to remember the rewarding effects of heroin/other drugs after this treatment. Mice will not, because they are not administering drugs to themselves. They are likely being administered drugs by an experimenter through an intravenous port.

This is not the same thing. That's not a drug addiction, that's a drug dependency.

Whether this will carry over into humans is something that is of interest for sure, but I wouldn't invest a lot of confidence into it personally. That's just me though, there's nothing wrong with being interested about the research at all. :)
 
Exactly, I wanted you all to see that.

The human mind is a precious thing and people don't understand quite how permanent the damage from ECT is.

I have not read a lot about ECT, but my understanding of it is that immediately afterward, you are going to have to re-learn how to live your life. It isn't uncommon to forget how to use the bathroom, how to feed/clothe yourself, how to talk/communicate.

The way you process/form memories is going to be forever altered. The only way this would be a "good thing" is if you were a violent sociopath and society wanted some way of recovering the body for a different soul, so to speak.

Thanks for the info CH. Before this I never even heard of ECT, I'm gunna do a little more reading, PM me if you have any particularly interesting reads, that's some crazy shit mang... 8o
 
Thanks for the info CH. Before this I never even heard of ECT, I'm gunna do a little more reading, PM me if you have any particularly interesting reads, that's some crazy shit mang... 8o

No problem! I actually do not know of much other interesting reading regrading it, so if you find anything interesting, feel free to send it my way as well.

What I copied and pasted was from the wikipedia article on ECT, I just didn't link to the original article.

http://en.wikipedia.org/wiki/Electroconvulsive_therapy
 
this forum is confusing to me. i didnt know where to put this. Ive tried iv ing subs and benedryl or diphenahydramine together. the effects were suppose to produce a better rush? i dont know but for me it didnt work the Ben gelled up. i wanted to know if anyone knows a better way to mix it up. Also I wanted to know if u could IV trazadone and bup. or i would like to IV by itself and see whats up?

Any help would be awesomely appreciated!
 
You really shouldn't IV pills without micron filtering them.

Benadryl probably isn't the most ideal antihistamine to IV, so I would suggest looking into micron filtering.

You won't get the same heroin type rush from antihistamines with buprenorphine but you can get somewhat of a rush with antihistamines, though it is probably not what you're looking for.

Also, please do not IV trazadone, it's not a drug worth IVing.
 
Back on day one again. I'm feeling ok, minus serious stomach ache. Minor chills but not too bad. I took 16mg today in 2mg doses spread out. Hopefullly stomach stuff calms down, I have some Immodium for that.

Also have ativan to sleep the first few days and some Propanolol
 
Trazadone not worth it is agreed i tried before looking at this thread and i agree 100%. It did absolutely nothing and i dont feel tired i must have done something wrong but im good wwith that . thanks for the help. Im a crazy micron wheel filter man. i just dont have any more.
 
Back on day one again. I'm feeling ok, minus serious stomach ache. Minor chills but not too bad. I took 16mg today in 2mg doses spread out. Hopefullly stomach stuff calms down, I have some Immodium for that.

Also have ativan to sleep the first few days and some Propanolol

Sorry to hear about the chills; those would drive me insane (that and goosebumps) - :| They will subside soon I am sure! I noticed the most annoying symptoms subside the quickest.

And good job on getting some Ativan, I really like it. It's the least sedating benzo in my opinion but it's still relaxing and it's nice because it's easily dissolving when taken sublingually.

I don't know if everyone gets this but I get *extremely* nauseous some times while on Suboxone. It's a very short lived thing but it's very annoying and I feel almost debilitated from the amount of pain and discomfort it causes.

Good luck Ashley and let us know how it goes! :)

Trazadone not worth it is agreed i tried before looking at this thread and i agree 100%. It did absolutely nothing and i dont feel tired i must have done something wrong but im good wwith that . thanks for the help. Im a crazy micron wheel filter man. i just dont have any more.

Glad to hear you use them when you have them.

The only antihistamine that I personally think is worth IVing with buprenorphine (that I have tried) is hydroxyzine hcl (Atarax). It definitely requires a micron filter because of all the inactive ingredients which are kind of chalky/nasty. What's good though is after micron filtering it with a 0.22um, it's completely clear.

The water solubility of trazodone is listed as "sparingly soluble"
http://drugbank.ca/drugs/DB00656
, and it orally has a high BA. So I reckon you did not get much trazodone in the shot.
 
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^^^^ i always use a o.22um wheel filter, but have only done it with oxycontin.

Is there a difference with filtering suboxone and subutex? how significant is the harm reduction is done with care? and also, is there much difference in the experience of Iv'ing either, in a recreational way as well as a harm reduction way
 
^^^^ i always use a o.22um wheel filter, but have only done it with oxycontin.

Is there a difference with filtering suboxone and subutex? how significant is the harm reduction is done with care? and also, is there much difference in the experience of Iv'ing either, in a recreational way as well as a harm reduction way

Yes, there is a difference. Suboxone will still retain some of its orange color. You can see it here: http://www.bluelight.ru/vb/showthread.php?t=481622

Subutex (brand name) is 100% clear when micron filtered with a 0.22um micron filter.

There is no difference in the subjective effects of either. I have tried both at equal mcg doses, exact same effects.

The difference with micron filtering is substantial - if you miss a shot after micron filtering it's not nearly as bad, doesn't hurt as much, and doesn't take as long to recover.

FDA approves seven-day transdermal patch for pain; 5, 10, & 20 micrograms of buprenorphine per hour

Source

Not a big deal IMO; the transdermal potency of buprenorphine is in the shitter.

This would only be useful for people with little/no opiate exp.
 
hehe IV trazadone and suboxone, ii was on trazodone for a couple years after i got it in treatment, took it for a couple years was great to sleep on except for the extreme fatigue waking up, i would warn caution about using it for too long after awhile it made me so i couldnt sleep. I just use 150mg valerian root, 50mg chamomile and .4 melatonin with 50 mg benadryl, weird ass dreams when it comes to traz to.

a couple times i got stomach aches on suboxone but they passed quickly probably 10 times if you count drinking on it(which im never doing again)

by the way I take 95% ethanol with my suboxone...about 2 mL per 8mg pill and i take 24 mg so thats 6 mL per day and i let it sit in my mouth with the sub for 45 minutes then swallow it, does alchohal it that amount cause any side effects when taken with suboxone? when i drank on subs it was never a good feeling which im glad for since i dont wanna kill myself so i dont drink anymore.
Do you guys swallow your alchohal with your subs. that is if you use the Ethanol sub mix
 
hehe IV trazadone and suboxone, ii was on trazodone for a couple years after i got it in treatment, took it for a couple years was great to sleep on except for the extreme fatigue waking up, i would warn caution about using it for too long after awhile it made me so i couldnt sleep. I just use 150mg valerian root, 50mg chamomile and .4 melatonin with 50 mg benadryl, weird ass dreams when it comes to traz to.

a couple times i got stomach aches on suboxone but they passed quickly probably 10 times if you count drinking on it(which im never doing again)

by the way I take 95% ethanol with my suboxone...about 2 mL per 8mg pill and i take 24 mg so thats 6 mL per day and i let it sit in my mouth with the sub for 45 minutes then swallow it, does alchohal it that amount cause any side effects when taken with suboxone? when i drank on subs it was never a good feeling which im glad for since i dont wanna kill myself so i dont drink anymore.
Do you guys swallow your alchohal with your subs. that is if you use the Ethanol sub mix

I spit it out and it only takes a few minutes for me to absorb, but I was only using 2mg per dose.

And I don't use Suboxone sublingually often anymore really so you might want to hear other people's opinions, but I think you should try tapering down over time, I think you'll still get a good effect out of less.
 
Yes, there is a difference. Suboxone will still retain some of its orange color.

There is no difference in the subjective effects of either. I have tried both at equal mcg doses, exact same effects.


Hey thanks heaps Captain:) I'm guessing the orange additive is a food colouring? or something thats not going to be an issue of harm with long term use?

Also, i have the same question about nalaxone being an issue over time with IV use?

I;m just wondering how much preference i should have between subutex and suboxone,,, if any.
 
Hey thanks heaps Captain:) I'm guessing the orange additive is a food colouring? or something thats not going to be an issue of harm with long term use?

Also, i have the same question about nalaxone being an issue over time with IV use?

I;m just wondering how much preference i should have between subutex and suboxone,,, if any.

Naloxone is inactive taken any ROA. Suboxone and subutex are essentially the same exact drug. I IV my suboxone 4 times a day. :D
 
yeah i hear they're basically the same since the bupe overpowers the naloxone at the receptors with suboxone. reason i say "i hear" is because im scripted suboxone but still haven't found any subutex to try and doc wont switch me over to the generic. :\ . ah oh well. im back to snorting but if i got a hold of a subutex i would use one of my .22 micron filters and try the utex out to see if there is a difference.
 
thanks captain I probably will taper down soon




yeah i hear they're basically the same since the bupe overpowers the naloxone at the receptors with suboxone. reason i say "i hear" is because im scripted suboxone but still haven't found any subutex to try and doc wont switch me over to the generic. :\ . ah oh well. im back to snorting but if i got a hold of a subutex i would use one of my .22 micron filters and try the utex out to see if there is a difference.

Im glad I take suboxone with nalaxone beause even though the nalaxone isnt active I have heard that Nalaxone reduces tolerance see here.

An interesting approach is the combination of opiates with the opiate antagonists naloxone or naltrexone in miniscule amounts. The combination of less than 0.001% of what would be a normal dose of the antagonist with an opiate allows a far greater response ("at least 50%") to the opiate which in turn permits a much lower effective dose to be used. It is also said to prevent respiratory depression, tolerance and addiction. This approach has apparently been patented (Crain & Shen 1996) and is being commercially developed by Pain Therapeutics. [R.A.H. 2000; Crain & Shen 2000


found this on erowid, now i imagine us people that take suboxone probably get .001% lol maybe a little more maybe a little less, and its fascinating to think that nalaxone which makes you go into withdrawals if used in miniscule amounts can help with tolerance and addiction thats one of my reasons for staying on suboxone lol.

heres the link if you wanna read more about it
http://www.erowid.org/chemicals/opiates/opiates_info3.shtml
 
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