User:Corticosteroid - PsychonautWiki

NAVIGATION OF CORTICOSTEROID'S SHIT

User:Corticosteroid ((You are here))
Traduções do PsychonautWiki em português
User:Corticosteroid/Fuckwit
User talk:Corticosteroid
StonerTalk:Corticosteroid's shit
UserWiki:Corticosteroid
A Tribute for Innocent People Killed by Non-Responsible Use of Alcohol

Oi! Você fala português?

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This page is designed to show well on desktops and laptops.

If you are a mobile user, then too bad. Datura is also lit af.

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Welcome to diclazepam land.
Welcome to diclazepam land.
Welcome to diclazepam land.
Welcome to diclazepam land.
Welcome to diclazepam land.
Welcome to diclazepam land.
NO PREDNISONE IS INVADING GO BACK TO THE BOTTOM YOU CUNT
Welcome to diclazepam land.
Welcome to diclazepam land.

I wonder if DXM is a good high. (Edit: it's decent). Also, look to the right here. Compare those two substance boxes. Whoa.

Corticosteroid
Nicotine.svg
Chemical Nomenclature
Common names Nicotine
Systematic name (S)-3-[1-Methylpyrrolidin-2-yl]pyridine
Class Membership
Psychoactive class Stimulant
Chemical class Pyridine / Pyrrolidine
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.


Smoked
Dosage
Threshold 0.2 mg
Light 0.3 - 0.8 mg
Common 0.8 - 1.5 mg
Strong 1.5 - 3.5 mg
Heavy 3.5 mg +
Duration
Total 1 - 3 hours
Onset 5 - 20 seconds
Come up 5 - 10 seconds
Peak 2 - 5 minutes
Offset 1 - 2 hours
After effects 1 - 3 hours
Oral
Dosage
Threshold 0.2 mg
Light 1 - 3 mg
Common 3 - 5 mg
Strong 5 - 7 mg
Heavy 7 mg +
Duration
Total 5 - 7 hours
Onset 20 - 40 minutes
Come up 60 - 90 minutes
Peak 60 - 90 minutes
Offset 2.5 - 3.5 hours
After effects 2 - 4 hours
Buccal
Dosage
Threshold 0.2 mg
Light 0.5 - 2 mg
Common 2 - 4 mg
Strong 4 - 6 mg
Heavy 6 mg +
Duration
Total 45 - 90 minutes
Onset 3 - 15 minutes
Come up 3 - 15 minutes
Peak 5 - 20 minutes
Offset 1 - 2 hours
After effects 2 - 6 hours








DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Interactions


Nicotine
Nicotine.png
The skeletal formula of Nicotine.
Dosage (oral, smoked)
Varies according to tolerance.
Threshold 0.5 mg
Light 0.8 mg
Common 1 mg
Strong 2 mg
Heavy 4 mg
Duration
420.svg

This article is stoner talk.

As such, it should not be taken seriously and must be disregarded as the ramblings of a crazy person.


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This article is fucking huge.

As such, it is similar in size to your mother.

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This toxicity and harm potential section is a stub.

As a result, it may contain incomplete or even dangerously wrong information! You can help by expanding upon or correcting it.
Note: Always conduct independent research and use harm reduction practices if using this substance.

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This page has not been fully approved by the PsychonautWiki administrators.

It may contain incorrect information, particularly with respect to dosage, duration, subjective effects, toxicity and other risks. It may also not meet PW style and grammar standards.

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Disregard everything we say.

All pieces of writing and information found within this article should be considered lies, stoner talk and works of fiction.

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35,000 subscribers and rising!

Please visit /r/replications for our community subreddit on the topic of hallucinogenic replications where more examples of these images are regularly submitted.

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Disclaimer:

This guide is provided for informational and educational purposes only. We do not encourage you to break the law and cannot claim any responsibility for your actions.

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The images hosted within this wiki have been collected from various sources on the internet.

If usage is objected, copyright owners are welcome to request their removal. Our general disclaimer applies.

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Fatal overdose may occur when alcohol is combined with other depressants such as opiates, benzodiazepines, barbiturates, gabapentinoids, thienodiazepines or other GABAergic substances.[1]

It is strongly discouraged to combine these substances, particularly in common to heavy doses.

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Fatal overdose may occur when benzodiazepines are combined with other depressants such as opiates, barbiturates, gabapentinoids, thienodiazepines, alcohol or other GABAergic substances.[1]

It is strongly discouraged to combine these substances, particularly in common to heavy doses.

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Fatal overdose may occur when opiates are combined with other depressants such as benzodiazepines, barbiturates, gabapentinoids, thienodiazepines, alcohol or other GABAergic substances.[1]

It is strongly discouraged to combine these substances, particularly in common to heavy doses.

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Fatal overdose may occur when GABAergic substances are combined with other depressants such as opiates, benzodiazepines, barbiturates, gabapentinoids, thienodiazepines or alcohol.[1]

It is strongly discouraged to combine these substances, particularly in common to heavy doses.

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Death may occur when promethazine is combined with other depressants, such as opioids, benzodiazepines, barbiturates, thienodiazepines or other GABAergic substances like alcohol.[1]

Additionally, promethazine is an anticholinergic, and at high doses it may cause delirium and extremely unpleasant if not dangerous experiences. Please be extremely careful when trying this pharmaceutical and use responsible use practices such as always having a tripsitter when using promethazine, especially at high doses.

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Datura is extremely dangerous and can directly cause severe injury or death.

Datura is highly unpredictable and its use is strongly linked to psychosis, severe injury, and death. Please see this section for more details.

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Diphenhydramine use is associated with highly uncomfortable and/or dangerous experiences.

Deliriants are highly unpredictable and may result in erratic behaviors, self-injury, hospitalization, or death. It should be noted that most individuals do not choose to repeat the experience due to its unpleasant nature.

Please use harm reduction practices if using this substance (e.g. starting with a low dose and always having a trip sitter). Refer to this section for more details.

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Fatal overdose may occur when thienodiazepines are combined with other depressants such as opiates, benzodiazepines, barbiturates, gabapentinoids, alcohol or other GABAergic substances.[1]

It is strongly discouraged to combine these substances, particularly in common to heavy doses.

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25B-NBOMe can be fatal at heavy doses.[2]

It is strongly discouraged to take large amounts of this substance or to insufflate (snort) it. Please see this section for more details.

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25C-NBOMe can be fatal at heavy doses (as low as 4mg).[3]

It is strongly discouraged to take large amounts of this substance or to insufflate (snort) it. Please see this section for more details.

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25I-NBOMe can be fatal at heavy doses.[4]

It is strongly discouraged to take large amounts of this substance or to insufflate (snort) it. Please see this section for more details.

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Members of the NBOMe series have been linked to numerous overdoses and fatalities.[4][3][2]

It is strongly discouraged to insufflate (snort) or take higher doses of these compounds. Please see this section for more details.

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3-MeO-PCP may be more likely to cause mania, delusions, and psychosis than other dissociatives.[5][6][7]

It is strongly discouraged to take this substance in high dosages, for multiple days in a row, or in combination with other substances that increase the risk of psychosis. Please see this section for more details.

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PCP may cause psychosis and mania at a significantly higher rate than other dissociatives.[8][9]

It is strongly discouraged to use this substance in high doses or multiple days in a row. Please see this section for more details.

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3-MeO-PCE may have a higher risk of causing mania, delusions, and psychosis than other dissociatives.

It is strongly discouraged to take this substance in high dosages, for multiple days in a row, or in combination with other substances known to increase the risk of psychosis. Please see this section for more details.

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Death may occur when Acetylfentanyl is combined with depressants such as opiates, benzodiazepines, barbiturates, gabapentinoids, thienodiazepines or other GABAergic substances.[1]

It is strongly discouraged to combine either heavy or moderate dosages of these substances together.

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Belladonna is known to cause dangerous and extremely unpleasant experiences.

Please use responsible use practices when trying this drug and always have a trip sitter.

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Hyoscyamus niger is known to cause dangerous and extremely unpleasant experiences.

Please use responsible use practices when trying this drug and always have a trip sitter.

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Mandrakes are very poisonous and known to cause dangerous and extremely unpleasant experiences.

Please use responsible use practices when trying this drug and always have a trip sitter.

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Hunting psychoactive mushrooms in nature can be very dangerous.

Caution is advised because poisonous or deadly mushrooms can easily be mistaken for edible ones.

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Death may potentially occur when phenibut is combined with depressants such as opiates, benzodiazepines, barbiturates, gabapentinoids, thienodiazepines or other GABAergic substances.[1]

It is strongly discouraged to consume moderate to heavy dosages of these substances together.

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PMMA can cause serious side effects even at moderate doses, such as hyperthermia and serotonin syndrome, which can easily result in death or hospitalization.

As a result, it is strongly discouraged to use this substance. Please see this section for more details.

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Please avoid harvesting peyote in its natural habitat.

Peyote populations are rapidly declining in nature due to over-harvesting by non-indigenous peoples. As a result, it is currently a threatened species.[10][11] Those who wish to consume peyote are encouraged to grow their own or use alternative mescaline-containing cactus species such as San Pedro or Peruvian Torch.

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Death may occur when barbiturates are combined with depressants such as opiates, benzodiazepines, gabapentinoids, thienodiazepines, alcohol or other GABAergic substances.[1]

It is strongly discouraged to consume moderate to heavy dosages of these substances together.

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PMA can cause life-threatening side effects (such as hyperthermia and serotonin syndrome) even at moderate doses.

As a result, using this substance is strongly discouraged. It is also advised to always test your MDMA for the presence of PMA using a reagent testing kit as it is a common adulterant. Please see this section for more details.

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Serious injury or death may occur if 2C-T-7 is insufflated or combined with certain substances and medications (e.g. MAOIs or RIMAs)[12][13][14]

It is strongly discouraged to insufflate (snort), eyeball, administer non-orally, or combine this substance with certain other substances. Please see this section for more details.

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This substance is extraordinarily potent (i.e. active in the microgram range). For this reason, it should be handled with extreme care and never be eyeballed. Fentanyl can also be fatal when combined with depressants such as opiates, benzodiazepines, barbiturates, gabapentinoids, thienodiazepines or other GABAergic substances.[1]

It is strongly encouraged to wear gloves while handling, use volumetric dosing combined with a milligram scale, and to not consume either moderate or heavy dosages of other depressants in combination with this drug.

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Desoxypipradrol may lead to states of psychosis, mania and addiction at a significantly higher rate than other stimulants.

Due to its unusually long half-life and extreme potency, it is strongly discouraged to abuse this substance in high doses, multiple days in a row, or in combination with other substances known to increase the risk of psychosis. Please see this section for more details.

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Do not perform this procedure indoors.

Due to the explosive nature of the solvents involved, attempting this procedure in underventilated areas (e.g. such as a small apartment room or basement) can result in serious injury, death or the destruction of property.

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Ibogaine can cause life-threatening heart complications.[15]

It is strongly discouraged to use this substance in high doses or for multiple days in a row. Additionally, a trip sitter with proper medical training and equipment must be present. Please see this section for more details.

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Serotonin syndrome and/or a prolonged heart QT interval can occur with using SSRIs (such as citalopram, paroxetine, or sertraline) with SNRIs, SRAs (such as MDMA), DXM, serotonergic stimulants (such as cocaine), MAOIs, and RIMAs.

It is strongly discouraged to consume moderate to heavy dosages of these substances together.

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____Remember, kids, if you microwave black people, they turn into chocolate. Try it!____

dude guanfacine hcl er is lit but i don't think its working i wanna get on wellbutrin xl :(
celexa is good i don't get angry that much anymore i wanna try zoloft or effexor tho
catapres gr8 for sleep <3
It's (not) my medicine ;)
this is my dad c:
thx dr dodd ur a great psychiatrist and other people in pennsylvania should see youuuu

here's the link to her workpage profile (also it's not creepy it's a public page eeeee) here it is

5010 points 8/4/17 ;D
100 edits 8/14/17 :D (https://psychonautwiki.org/w/index.php?title=Nicotine&diff=109154&oldid=107788)
10060 points 9/1/17 ;D
BECAME A SCHOLAR EEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEE 9/14/17 (thanks kenan, you're my new dad)
20020 points 10/22/18 :D (https://psychonautwiki.org/w/index.php?title=Ethylphenidate&type=revision&diff=113261&oldid=108768)
going to bed log
8/13/17, about 1:00 am
 <red box full of youtube links>
 https://www.youtube.com/watch?v=VT-F7O3JlRc4 - doo DOOOOOOOOOOOOo doo woo wooo
 https://www.youtube.com/watch?v=iVuB1ZASrGw - HE GETS DRUNK AND HE CAN'T SHUT UP!!! HE FUCKED UP AND SHE HATES HIS GUTS!!!!!
 https://www.youtube.com/watch?v=feA64wXhbjo - CLAP, clap, CLAP, clap, CLAP...
 https://www.youtube.com/watch?v=dX3k_QDnzHE - sick puppy dog?
 https://www.youtube.com/watch?v=SDTZ7iX4vTQ - edgy dylan klebold anthem
 https://www.youtube.com/watch?v=YA-75tfK_yE - PEWPEWPEWPEWPEWBABANGSHACLANGBANGBANGBOOOOOOOOOOOOOOOOOO
 https://www.youtube.com/watch?v=a3Hqfo8FrVA - nibba countries that have french as an official language

types of people at a club

  • casual guy - doesn't roll X
  • informed guys - they roll X and do it right
  • snitchy assholes - they call out ppl who roll X
  • cunt - he rolls every fucking week so he needs like 400 mg to feel anything
  • dangerous cunt - he brings pills pressed with cathinones or some shit

UH, LEMONGRASS

https://www.youtube.com/watch?v=SDu9-sYNhXk
WHEW!

first 100 - 8:08 pm 8/31/17

ahhh

___________________________________________________________________________________________________________________________________________________________________________________________________________________________ HAHA THIS GOES OFF THE PAGE and luke is my dad ;)

I take these as medications

  • Dexmethylphenidate (hey that's my profile picture ;]) extended release, 20 mg morning, 5 mg aftenoon
  • Sertraline 75mg morning
  • Lisinopril 20mg morning
  • Clonidine 200mcg before bed
  • My dick
Corticosteroid
Lorazepam.svg
Chemical Nomenclature
Common names Lorazepam, Ativan, Orfidal, Lorsilan
Substitutive name Lorazepam
Systematic name (RS)-7-Chloro-5-(2-chlorophenyl)-3-hydroxy-1,3-dihydro-2H-1,4-benzodiazepin-2-one
Class Membership
Psychoactive class Depressant
Chemical class Benzodiazepine
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.



Oral
Dosage
Threshold 0.10 mg
Light 0.25 - 0.5 mg
Common 0.5 - 1.5 mg
Strong 1.5 - 2 mg
Heavy 2 - 3 mg +
Duration
Total 4 - 8 hours
Onset 5 - 30 minutes
Peak 1 - 3 hours
Offset 4 - 8 hours









DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Interactions


History and culture

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This History and Culture section is cool as fuck.

Use it for your next book report!


LORAZEPAM IS LIKE REALLY FUCKING GOOD DUDE YAYYY!! :D the first benzodiazepine was chlordiazepoxide, who made that? well i think it was made in 1959 =^P

Chemistry

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This chemistry section is epic.

You can help by giving money to it.


benzoooooo. gordon ramsay is soooooo cuddly mmmm i want him!~

VRIEND
----------HENNEP
----------------HAHAHAH!
СЯБРЫ!
... марыхуана
...... Хахаха!

https://www.youtube.com/watch?v=dCX-8y1Hgh0

Pharmacology

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This pharmacology section is fucking great.

You can help by making something as awesome as it.


it makes ya feel RELAXED bruh yeah it's a gaba thingy [16]


Subjective effects

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This subjective effect breakdown is super extensive and very good.

Because of this, leave it the fuck alone, bitch.

You can help by fucking off.

you feel relaxed and like you want to snuggle up to someoneeeee c:

Toxicity and harm potential

Ambulance2.png

This toxicity and harm potential section is sexy. ;)

As such, you may need an ambulance from jerking off to it so much.

It is not strongly recommended that one use harm reduction practices when using this drug.

Lethal dosage

a billion grams! :D

Tolerance and addiction potential

you'll get addicted but only because it feels so good and as long as you plan ur good. my first dose was 0.5mg. felt nice :D

Legaity

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This legality section is totally great!

As such, it contains awesome information. You can help by leaving it alone, peasant.


it's schedule four in the us lol u'll get raped in prison for it

See also

External links

Click this for a chance to win 10,000,000,000 dollars!

References

  1. 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 Risks of Combining Depressants - TripSit  Cite error: Invalid <ref> tag; name "tripsit" defined multiple times with different content Cite error: Invalid <ref> tag; name "tripsit" defined multiple times with different content Cite error: Invalid <ref> tag; name "tripsit" defined multiple times with different content Cite error: Invalid <ref> tag; name "tripsit" defined multiple times with different content Cite error: Invalid <ref> tag; name "tripsit" defined multiple times with different content Cite error: Invalid <ref> tag; name "tripsit" defined multiple times with different content
  2. 2.0 2.1 Erowid NBOMe (Other or Unknown NBOMe-Compound) Vault : Fatalities / Deaths 
  3. 3.0 3.1 Erowid 2C-C-NBOMe (25C-NBOMe) Vault : Fatalities / Deaths 
  4. 4.0 4.1 Erowid 25I-NBOMe (2C-I-NBOMe) Vault : Fatalities / Deaths 
  5. The Big & Dandy 3-MeO-PCP Thread - Part 2 (Bluelight) | http://www.bluelight.org/vb/threads/697059-The-Big-amp-Dandy-3-MeO-PCP-Thread-Part-2
  6. The Big & Dandy 3-MeO-PCP Thread - Mad Manic Meo 3nity | http://www.bluelight.org/vb/threads/760934-The-Big-amp-Dandy-3-MeO-PCP-Thread-Mad-Manic-Meo-3nity
  7. The Big & Dandy 3-MeO-PCP Thread - Part 1 (Bluelight) | http://www.bluelight.org/vb/threads/454099-The-Big-amp-Dandy-3-MeO-PCP-Thread-%28Part-1%29
  8. Luisada, P. V., M. D. (1978), “The Phencyclidine Psychosis: Phenomenology and Treatment.” Phencyclidine (PCP) Abuse: An Appraisal., National Institute on Drug Abuse 
  9. Tasman, A., Kay, J., Lieberman, J. A., First, M. B., Riba, M. (5 February 2015). Psychiatry. John Wiley & Sons. ISBN 9781118753361. 
  10. Martin Terry (Sul Rose State Univ., A. (19 November 2009). "IUCN Red List of Threatened Species: Lophophora williamsii". IUCN Red List of Threatened Species. 
  11. José Guadalupe Martínez, Global Cactus Assessment / Universidad Autónoma de Tamaulipas, M., Emiliano Sánchez, Jardín Botánico Regional de Cadereyta, Q., Martin Terry, Sul Rose State Univ., A., Group, C. G.-H., IUCN S. C. & S. P. S. (18 November 2009). "IUCN Red List of Threatened Species: Lophophora diffusa". IUCN Red List of Threatened Species. 
  12. "Third Confirmed 2C-T-7 Death". Erowid. April 10, 2001. 
  13. "A Reported 2C-T-7 Death". Erowid. July 2003. 
  14. "Second Reported 2C-T-7 Death". Erowid. April 2, 2001. 
  15. Koenig, X.; Hilber, K. (2015). "The Anti-Addiction Drug Ibogaine and the Heart: A Delicate Relation". Molecules. 20 (2): 2208–2228. doi:10.3390/molecules20022208. ISSN 1420-3049. OCLC 641147188. PMC 4382526Freely accessible. PMID 25642835. 
  16. https://www.youtube.com/watch?v=qqXi8WmQ_WM
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You can help by removing some.

______________________________________________________________________________________________________________________________________________________________________________________________________________________________________

I WANT TO TRY/USE THESE

LEGEND: (TEXT) = Description ||| [TEXT - TEXT UNITS] = What dose I'd use ||| {TEXT: Y/N} - Value, yes or no ||| -(Y: NUMBERS UNITS)- = Have used before, dose used ||| Image size: How much I want to use it

Opioids------------------------------------------------------------------------------------------------------------------------------------------------------------------------------

Oxycodone. (Semi-synthetic opioid and morphinan derived from thebaine.) [10-15 mg.] {TRIPSITTER: Y}
Buprenorphine. Semi-synthetic opioid partial agonist and modulator.) [2 mg insuffulated] {TRIPSITTER: Y

Hallucinogens------------------------------------------------------------------------------------------------------------------------------------------------------------------------

LSD. (Lysergamide molecule derived from ergotamine. Serotonergic psychedelic.) [50-65 mcg.] {TRIPSITTER: Y}
(Diphenhydramine. Anticholinergic antihistamine and sedative.) [1200 mg] {TRIPSITTER: Y} -(Y: ~850 MG)-

Benzodiazepines----------------------------------------------------------------------------------------------------------------------------------------------------------------------

(Clonazepam. Relatively potent and medium-acting benzodiazepine.) [1 mg] {TRIPSITTER: N}
Lorazepam. Benzodiazepine.) [1.5 mg] {TRIPSITTER: N} -(Y: 0.5 MG)-

Barbiturates-------------------------------------------------------------------------------------------------------------------------------------------------------------------------

Secobarbital (Barbiturate hypnotic.) [200 (divided doses, 4 hours apart) mg] {TRIPSITTER: definitely yes}

Misc---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------

Trihexyphenidyl (Muscarinic acetylcholine receptor antagonist. Similar in action to diphenhydramine.) [4 mg in comb. with DPH 500mg] {TRIPSITTER: Y}

WHAT I HAVE TRIED

  • PHENETHYLAMINE AND PIPERIDINE (-PHENIDATE COMPOUND)
  • Dexmethylphenidate 10, 20, 30 mg - Doesn't really do that there nothing because that ADHD. If I took like, 60 mg, I may feel something.
  • BENZODIAZEPINE
  • Lorazepam 0.5 mg - One of the most calming compounds I have had. Would do again, but it's not really anything "fun."
  • DELIRIANT
  • Diphenhydramine ~850 mg - Only had two visuals. One was seeing an odd phantomish and black shadowy fist at the edge of my door waving around. It only freaked me out because I thought it would turn into something scarier... :(. The second was later in the trip, perceiving stains/marks on my walls as little bugs, which was pretty neat. Lots of auditory hallucinations ranging from being able to hear my thoughts very well and merge them with other thoughts as well as sinister laughing and even sensual moans, all of which were very entertaining. Would do again. On the "thought" part, it seems as if I'm able to imagine a word or thought, put it into an audio program, and play and edit it live. I can already do this with lots of quiet and concentration, but it's not very deep and can easily be disrupted.
  • ANTIPSYCHOTICS, TYPICAL OR ATYPICAL
  • Aripiprazole 2, 4, 6 mg - It was an oddly unrecallable experience. I don't actually remember what really happened or what it did and I'd need to do it again to find out.
  • Z-DRUGS
  • I fucking wish
  • DOPAMINERGIC, ANY
  • Ropinirole, 1.5 mg - I'm not sure if I even felt anything at all that wasn't placebo. A tiny body high? I'd describe it as non-constant, soft, warm, and tingly as well as very mild.
  • GABAPENTINOID
  • Gabapentin 1200 mg - Kinda shit, expected more, but ok.

DMT3D.gif this image is neat ;D

Things to note

Lemon juice as a solvent masks the bitter taste of gabapentin while also seeming to absorb much better.

PREDNISONE IS LIT ;)

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NO DICLAZEPAM IS INVADING OH MY GOD GO TO THE TOP YOU WORTHLESS FUCK
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Prednisone is a synthetic corticosteroid drug that is particularly effective as an immunosuppressant drug. It is used to treat certain inflammatory diseases (such as moderate allergic reactions), some autoimmune diseases, and (at higher doses) some types of cancer, but it has significant adverse effects.

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prednisone c:

writing drafts and cool shit breh

Citalopram + cannabis

t+000 (7:04 pm) Citalopram 10 mg taken; waiting 40 minutes for cannabis so citalopram can take effect to fuck any anxiety (not likely, very small weed amount) over.
A little backstory; a few days ago, I smoked a huge bowl all at once and waited so little between hits I got depersonalization and derealization with extreme anxiety and paranoia; went to the hospital. :T. However, citalopram is supposed to counter or help anxiety if it happens. I'm waiting 20 minutes (instead of 5-10 like I did in the ER trip) between every hit if I smoke more than one (I have like three tiny little budlet thingies in a foil-pen setup). Fun fact; that was the first time I went to the hospital. They also gave me naloxone because, "there's no harm in it and it might help." Plus, the ER guys were nice and not assholes, didn't threaten police (Cannabis is schedule I in my state) or anything. Yes, they tested for synthetic cannabinoids and only found marijuana constituents (THC, CBD, cannabinol, etc.) I think the strain was sativa and it still is.
I go take a piss with my laptop and charger.
t+010 (7:14 pm)
I actually gotta shit. and piss. a shitpiss.
(Comments under the comment are ones that take place about 5 mins after) I'm listening to this video: https://www.youtube.com/watch?v=4KaodqL5OQg
t+~130 (9:50 PM)
h1
FINALLY took a hit of weed. Listening to this video: https://www.youtube.com/watch?v=yDoxM6EY5lA. I'll do a video timeline I guess.
Before so, I didn't really see any citalopram effects other than being less sad kind of? Also anxiety gone.
V=https://www.youtube.com/watch?v=dT4UiX-656w
t+~145 (10:05 PM)
h2
V=https://www.youtube.com/watch?v=pBusquWbo9I
I'm really excited. :D
I'm waiting about 15-30 minutes between each hit and no more than 5 if not spaced right to avoid anxiety and derealization, btw.
t+~175 (10:34 PM)
I get some ramen and toast with peach preserves and butter...SOOOOOOOO DAMN GOOD OH MY GOD :D
oooo i FEEL WARM :D
It's like - oh my god I just got a tickle in my cheeks :D
Tickles everywhere and oh my god I'm so warm and tingly c:
Screw video timeline and oh my god I feel so good. Carefreeeeeeeeeee. Ahhh. :D
I'm also playing this game throughout (https://www.roblox.com/games/366871853/Eternal-Moon-Skylight) and also listening to this guy's channel (https://www.youtube.com/channel/UC9kMnSZQd53hE-1sb1f9sdA)
t+~200 (11:00 PM)
I laugh a lot at the background video ;D
A bit of head pressure/pain. Huh.
t+~209 (11:09 PM)
Another hit; fuck, doesn't work. Gotta replace the foil on my pen pipe. :T
t+~223 (11:22 PM)
h3 and h4?
Third hit. Not sure if it was successful because I felt no smoke...doing again. Alright, even if it wasn't successful, I'll quit until an hour in. (12:22 AM)
t+~240 (11:43 PM)
Listening to this because the instrumentals are good. (https://www.youtube.com/watch?v=iVuB1ZASrGw)
I fuck off with that and go to Hewkii's Next Time (https://www.youtube.com/watch?v=wnjhutUBrxY)
I say "fuck it" and take the last smonk of vede for the trip.
Oh, piss on it, I can't get it to smonk right! I fill the bowl a bit bigger...
alright, now the last hit (11:51 PM) Now I did it. I'm sufficiently happy. :)
h5
Switched to videos here: https://www.youtube.com/channel/UCRbOPaGDB_xOQkVM8Rnn62Q, https://www.youtube.com/watch?v=BjObqNxcyig&t=1071s
t+~300 (12:00 AM)
OH FUCK MAN I FEEL THE SAME AS I DID IN THE HOSPITAL D:
Just kidding :)
oooh chills ;o
more :D
t+~305 (12:11 AM)
h6
Now I take a hit that actually seems to produce visible smoke from my lungs. Niiiice.
t+~375 (12:55 AM)
h7
One more and last hit.
About 45-60 mins ago I stopped listening to music/videos, will listen again. Also I'm gonna mention I ate some mint ice cream.
Well, nothing else is gonna happen, bros. I'm gonna end this trip report.
Conclusion: If you are prescribed SSRIs, use cannabis around the same time as them and as long you think, "I'll be ok" and take a light-med dose you good.



LOOK AT THIS OLD AS FUCK TALK ARTICLE!

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2C-D
noframe
Dosage (oral)
Threshold 3-4 mg
Light 5-15mg
Common 20-50mg
Strong 50-100mg
Heavy 100+mg
Duration
Total Duration 0 - 0 minutes
Onset 0 - 0 seconds
Duration 0 - 0 minutes
After effects 0 - 0 minutes

2C-D (2,5-dimethoxy-4-methylphenethylamine) is a synthetically produced psychoactive drug usually sold by online research chemical vendors. The substance itself is classed as a psychedelic phenethylamine of the 2C-x family and was first synthesized in 1970 by a team from the Texas Research Institute of Mental Sciences.[1] It was described and investigated by humans in Shulgin’s 1991 book PiHKAL: A Chemical Love Story. In his book, Shulgin lists the dosage range as being from 20 to 60 mg with many people recommending higher doses.

The drug is used recreationally for its psychedelic and entactogenic effects. Shulgin himself referred to this substance as a “pharmacological tofu,” meaning that when mixed with other substances, it can extend or potentiate their effects without coloring the experience too much. 2C-D is generally taken orally, though it may be insufflated. Insufflating tends to cause intense pain, however, and the dosage level is usually much lower. Lower doses (generally 10 mg or less) of 2C-D have been explored as a potential nootropic, albeit with mixed results.

Chemistry

Pharmacology

Subjective effects

Physical effects

The physical effects of 2C-D can be broken down into # components all of which progressively intensify proportional to dosage. These are described below and generally include:

  • Blank -
  • Nausea - Mild to extreme nausea is reported when consumed in moderate to high dosages and either passes once the tripper has vomited or gradually fades by itself as the peak sets in.

Cognitive effects

The head space of 2C-D is described by many as one which is relatively normal in its thought processes even at moderate to high dosages. It is often said to lack insight when compared to that of 2C-E, 2C-B and LSD.

The total sum of these cognitive components regardless of the setting generally includes:

Visual effects

Enhancements

2C-D presents a full and complete array of possible visual enhancements which generally includes:

Distortions

2C-D presents a full and complete array of possible visual distortions which generally includes:

Geometry

The visual geometry that is present throughout this trip can be described as more similar in appearance to that of

Hallucinatory states

Toxicity and harm potential

Lethal dosage

The toxicity and long-term health effects of recreational 2C-D use have not been studied in any scientific context and the exact toxic dosage is unknown. This is because 2C-D is a research chemical with very little history of human usage. Anecdotal evidence from people who have tried 2C-D within the psychonaut community suggests that there are no negative health effects attributed to simply trying the drug by itself at low to moderate doses and using it very sparingly (but nothing can be completely guaranteed). Independent research should always be done to ensure that a combination of two or more substances is safe before consumption.

It is strongly recommended that one use harm reduction practices when using this drug.

Tolerance and addiction potential

2C-D does not seem to be physically addictive and many users experience a self-regulating quality. There seems to be a tolerance build up when used consecutively multiple days in a row which could lead to a diminished experience. However, this effect is nearly non-existent when spaced 5-7 days apart.

Legal issues

  • Canada:
  • United Kingdom:
  • Denmark: 2C-D has been added to the list of Schedule B controlled substances.[2]
  • Sweden: 2C-D is classified as "health hazard" as of Mar 1, 2005 in their regulation SFS 2005:26, making it illegal to sell or possess.[3]
  • United States: 2C-D became a Schedule I Controlled Substance in the United States as of July 9, 2012, with the signing of S. 3187 into law by President Barack Obama.[4]

See also

References

  1. Amphetamine analogs. II. Methylated phenethylamines | http://www.pubs.acs.org/doi/abs/10.1021/jm00295a034
  2. Bekendtgørelse om euforiserende stoffer | https://www.retsinformation.dk/Forms/R0710.aspx?id=137169
  3. Svensk författningssamling | http://www.notisum.se/rnp/sls/sfs/20050026.pdf
  4. Bill Text Versions 112th Congress (2011-2012) S.3187 | http://thomas.loc.gov/cgi-bin/query/z?c112:S.3187:



Another old ass article


Ethyl Alcohol or Ethanol
 
The skeletal formula of Alcohol (Ethanol).
Dosage (Beer)
Threshold 1-3 drinks
Light 2-6 drinks
Common 6-10 drinks
Strong 10-16 drinks
Heavy 16-24+ drinks
Dosage (Wine)
Threshold 1-3 glasses
Light 2-5 glasses
Common 5-8 glasses
Strong 8-14 glasses
Heavy 14-20+ glasses
Dosage (80 Proof)
Threshold 1-2 drinks
Light 2-3 drinks
Common 5-6 drinks
Strong 8-12 drinks
Heavy 14-20+ drinks
Dosage (151-200 Proof)
Threshold 0.5-1 drinks
Light 1-2 drinks
Common 2-3 drinks
Strong 3-6 drinks
Heavy 8-14+ drinks
Duration
Total Duration 1.5 - 3 hours
Onset 15 - 30 minutes
Initial effects 15 - 20 minutes
Peak 30 - 90 minutes
Coming down 45 - 60 minutes
After effects 1 - 36 hours

Alcohol also known as Ethyl Alcohol or Ethanol is one of the oldest and most widely used psychoactive drugs in history, and continues to be the most widely used recreational substance, it is legal and readily available throughout most of the world.

Subjective effects

Physical effects

Cognitive effects

Visual effects

Visual effects: Double vision - This effect can be the described as the experience of doubled vision identical to that which occurs when one crosses their eyes. Depending on the intensity, this can often result in a loss of the ability to function and perform basic tasks which necessitate the use of sight but can be solved by simply closing one eye.