I didn't notice that hammer had linked to the side effects. Had I noticed I might have posted them anyway since he already linked to them and it was relevant to his concerns. Most people post here because they enjoy discussing information other people post.
This issue is not my hobby horse, I don't like back and forth word games that hinge on creative interpretation, but since i'm not doing anything important at the moment, and my remarks were not sensitive, wrong, seriously dangerous, a product of my own limitations, heedless without excuse, construed as advice, incorrectly defined, nonsense, un-information, bullshit, imposing orthodoxy, and at an expense to health, I am willing to examine them further for accuracy.
eyeno wrote:
Hey hammer of los. Best wishes to you brother. I don't know if you have looked this up but if you haven't I am delivering it to your plate for your consumption.
Bottom line in a nutshell is that you
might expect metabolic disturbance from Olanzapine. Metabolic disturbance
denotes toxicity happening in the body.
I like your valerian idea, A LOT
Not giving medical advice but this is the possible consequences of Olanzapine, and not sure I like the way it reads.
I hope the valerian works for you bro.
As with all neuroleptic drugs, olanzapine can cause the (sometimes) irreversible movement disorder tardive dyskinesia, and the rare, but life-threatening, neuroleptic malignant syndrome. Some also associate all antipsychotics with permanent brain damage.[20]
Other recognised side effects may include:
akathisia; inability to remain still (restlessness)[21]
dry mouth
dizziness
irritability
sedation
insomnia
constipation
urinary retention
orthostatic hypotension
weight gain
increased appetite
runny nose
impaired judgment, thinking, and motor skills
impaired spatial orientation
impaired responses to senses
seizures
trouble swallowing
dental problems and discoloration of teeth
missed periods
problems with keeping body temperature regulated
apathy, lack of emotion
Endocrine side effects have included hyperprolactinemia, hyperglycemia, and diabetes mellitus
Brain Zaps
Auditory Hallucinations[22]
[edit] Metabolic effects
The Food and Drug Administration requires all atypical antipsychotics to include a warning about the risk of developing hyperglycemia and diabetes, both of which are factors in the metabolic syndrome. These effects may be related to the drugs' ability to induce weight gain, although there are some reports of metabolic changes in the absence of weight gain.[citation needed] Studies have indicated that Olanzapine carries a greater risk of causing and exacerbating diabetes than another commonly prescribed atypical antipsychotic, Risperidone. Of all the atypical antipsychotics, olanzapine is one of the most likely to induce weight gain based on various measures.[23][24][25][26] The effect is not dose dependent.[dubious – discuss] Olanzapine may directly affect adipocyte function, promoting fat deposition.[27] There are some case reports of olanzapine-induced diabetic ketoacidosis.[28] Olanzapine may decrease insulin sensitivity.[29] though one 3-week study seems to refute this.[30] It may also increase triglyceride levels.[24]
Recent studies have established :
that Olanzapine and Clozapine disturb the metabolism by making the body take preferentially its energy from fat (instead of privileging carbohydrates). Thus, levels of carbohydrates remaining high, the body would develop insulin resistance (reduction of insulin sensitivity).[31]
that Olanzapine promotes fat accumulation : due to disturbances in fat metabolism, rodents become fatter (but don't have their weight increasing at first). Being fatter, they do less exercise, burning less fat and gaining weight.[32]
Despite weight gain, a large multi-center randomized National Institute of Mental Health study found that olanzapine was better at controlling symptoms because patients were more likely to remain on olanzapine than the other drugs.[33] One small, open-label, non-randomized study suggest that taking olanzapine by orally dissolving tablets may induce less weight gain,[34] but this has not been substantiated in a blinded experimental setting.
[edit] Animal toxicology
In a placebo-compared study of six Macaque monkeys receiving olanzapine between 17 and 27 months, a significant brain volume and weight decreases (8-11%) were detected.[35] In latter studies of the stored samples, the changes were attributed to astrocyte and oligodendrocyte loss,[36] with the neurons spared but positioned more closely compared to the controls.[clarification needed] However according to this study the neurons do not seem to be completely spared. The gray matter shrinking found was 14.6%, but the neuron density increase was only 10.2% which corresponds to approximately a loss of 5% of the neurons.[citation needed]
Olanzapine has demonstrated carcinogenic effects in multiple studies when exposed chronically to female mice and rats, but not male mice and rats. The tumors found were in either the liver or mammary glands of the animals.[37]
[edit] Discontinuation
The British National Formulary recommends a gradual withdrawal when discontinuing anti-psychotic treatment to avoid acute withdrawal syndrome or rapid relapse.[38] Due to compensatory changes at dopamine, serotonin, adrenergic and histamine receptor sites in the central nervous system, withdrawal symptoms can occur during abrupt or over-rapid reduction in dosage. Withdrawal symptoms reported to occur after discontinuation of antipsychotics include nausea, emesis, lightheadedness, diaphoresis, dyskinesia, orthostasis, tachycardia, nervousness, dizziness, headache, excessive non-stop crying, and anxiety. The present evidence suggests that these symptoms affect a small number of susceptible individuals treated with antipsychotics.[39][40] Complicated and long-lasting rebound insomnia symptoms can occur after withdrawing from antipsychotics.[citation needed]
[edit] Overdose
Symptoms of an overdose include tachycardia, agitation, dysarthria, decreased consciousness and coma. Death has been reported after an acute overdose of 450 mg, but also survival after an acute overdose of 1500 mg.[41] There is no known specific antidote for olanzapine overdose, and even physicians are recommended to call a certified poison control center for information on the treatment of such a case.[41] Prescription should be kept in small quantity to reduce risk overdose as acute bipolar disorder and schizophrenic patients can be at a high risk of suicide (Eli Lilly 2010
https://secure.wikimedia.org/wikipedia/ ... Olanzapine
Which extrapolated into:
compared2what wrote:
I think what you're doing is wrong and seriously dangerous. What would you want me to do about what I believed, based on conviction, information and thorough consideration, to be a serious danger? Ignore it?
compared2what wrote:
You posted medical information out of context that you don't understand and aren't qualified to advise people about, along with a false (or maybe just ignorantly erroneous) statement about a medication's toxicity. You also posted only the potentially adverse effects of taking it, as if there was no possibility of benefit. Which is bullshit.
compared2what wrote:
You were addressing someone who had himself not only ALREADY linked to the information source you were cutting and pasting from, but also made a comment indicating that he knew what the side effects were AT THE VERY SAME TIME.
Didn't notice. Gave him benefit points for obvious intelligence
compared2what wrote:
It's not showing concern or respect or sensitivity for other people to do that, eyeno. It's imposing your othodoxy on them, possibly at the expense of their health and well-being.
compared2what wrote:
You added your own personal little definition of metabolic disturbance, which you evidently think of as another term for "toxicity." That was not true or good information. It was, in fact, uninformation.
compared2what wrote:
eyeno, you have a moral imperative to be more sensitive to the dangers posed by your own limitations than that. Under all circumstances. Without exception.
compared2what wrote:
No. You could be the greatest living expert on Zyprexa and metabolic disturbance in the world today. You still wouldn't be doing anything but endangering others by handing out advice about it on the internet without one word of qualification or demurral. You don't even know the proposed dosage.
compared2what wrote:
You're doing something that's wrong. I decry the wrong act.
compared2what wrote:
I don't doubt your good intentions. But they don't excuse your heedlessness. Nothing does. And nothing could. You should know better.
compared2what wrote:
You also added some remarks that might have been about metabolic disturbance if you hadn't gone on to define it wrongly and -- in fact -- nonsensically.
Wow. That is a ton of heathen behavior right there.
I specifically used the terminology I used because it is the same terminology used by medical professionals that study Olanzapine. It is correct and it is accurate. Example:Protection from olanzapine-induced metabolic toxicity in mice by acetaminophen and tetrahydroindenoindole.Shertzer HG, Kendig EL, Nasrallah HA, Johansson E, Genter MB.
Department of Environmental Health and Center for Environmental Genetics, University of Cincinnati Medical Center, Cincinnati, OH 45267-0056, USA.
shertzhg@ucmail.uc.eduAbstract
OBJECTIVE:
In mice and in humans, treatment with the second-generation antipsychotic drug olanzapine (OLZ) produces excessive weight gain, adiposity and secondary metabolic complications, including loss of glucose and insulin homeostasis. In mice consuming a high-fat (HF) diet, a similar phenotype develops, which is inhibited by the analgesic acetaminophen (APAP) and by the antioxidant tetrahydroindenoindole (THII). Therefore, we examined the ability of APAP and THII to prevent metabolic changes in mice receiving OLZ.
http://www.ncbi.nlm.nih.gov/pubmed/20065957
Seems pretty straightforward to me. Metabolism and toxin all wrapped in a neat little package. I had previously studied Olanzapine in the past. I forgot most of it but I did remember some of it. I already knew it was a toxin. By the very nature of what it is and does to the body it qualifies as a poison and toxin.
This following is the context and my understanding of the terms I used, and their associations in context to the subject.
"Metabolic disorder" any pathophysiologic dysfunction that results in a loss of metabolic control of homeostasis in the body. It is a term used by researchers of Olanzapine. "Disturbance" qualifies. Disturbance denotes a migration from normal or comfortable order.
Metabolism: the set of chemical reactions that happen in the cells of living organisms to sustain life.
Toxin: A poison formed as a specific secretion product in the metabolism of a vegetable or animal organism, as distinguished from inorganic poisons. Such poisons can also be manufactured by synthetic processes. (wiki)
I don't remember everything I learned about Olanzapine, but other information I remember, and refer back to with a little internet memory refreshment help includes:
creatine kinase: An enzyme present in muscle, brain, and other tissues of vertebrates that catalyzes the reversible conversion of ADP and phosphocreatine into ATP and creatine. Creatine kinase (CK), also known as creatine phosphokinase (CPK) or phospho-creatine kinase
Clinically, creatine kinase is assayed in blood tests as a marker of myocardial infarction (heart attack), rhabdomyolysis (severe muscle breakdown), muscular dystrophy, the autoimmune myositides and in acute renal failure.
Elevation of CK is an indication of damage to muscle. It is therefore indicative of injury, rhabdomyolysis, myocardial infarction, myositis and myocarditis. (wiki)
Elevated creatine kinase is often found in patients treated with Olanzapine. All that muscle jerking often associated with this medication doesn't happen for no reason. Something bad is happening. I don't understand the exact mechanism behind it but the above is a clue and takeoff point that could be used to study it further. Elevated creatine kinase is often found in patients treated with Olanzapine and it "might" or "could" be a sign that something is being
destroyed.
I don't expect every patient that takes Olanzapine to suddenly drop dead or be impaired for life. Some may derive benefit from it. But, I like hammer enough that I thought of these things. For his safety I wanted to make sure he was aware.
The Hammer Man has been busy dancing and singing and I wasn't sure if he had taken time out to examine these possibilities. I didn't notice that he had linked to them already.
If this is considered by some as: not sensitive, wrong, seriously dangerous, a product of my own limitations, heedless without excuse, construed as advice, incorrectly defined, nonsense, un-information, bullshit, imposing orthodoxy, and at an expense to health, considering that my terminology was accurate and correct, I will simply have to disagree that it is any of these things. And the next time I see someone getting ready to swallow something toxic, regardless if it be drugs, food, herbs, or gasoline, I will feel compelled to tell them it is poisonous.
Love you Hammer and I would love to watch you dance and sing in your costume complete with wand. I bet its a trip.