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psx:substance/ketamine/value/timeline/intramuscular/afterglow@1

valuereferenced by edges — no row of its own

derived from · upstream

feeds · downstream

none recorded

Closure of psx:substance/ketamine/value/timeline/intramuscular/afterglow@1: 1 upstream, 0 downstream.

psx:substance/ketamine/value/timeline/intramuscular/afterglow@1
└─ derived_from  proposal/timeline/e682ffdf-0201-4774-a96b-99d5f71c1f27  timeline · intramuscular · afterglow

indented by distance from this node, not by parentage

1Provenance card

the boundary, as counts

Sources

4942 with DOI

23 strong · 21 moderate · 5 weak

Compilations

22026-04-20T09:52:08.318Z

pipeline-v5 · prompt hash not recorded — run predates 2026-09 · 1 other run

Decisions

62last ruled 2026-06-04

0 awaiting a ruling

Issued documents

42026-10-19T20:32:25.864Z

notice · info card · emergency

Searches

250 with no results

queries and counts on the build

Claims checked

19923 supported

23 supported · 176 not

Correspondence

0received

consent field ships in Phase 4

Edges

545

derivations recorded for this entity

Complete over 49 sources, 2 compilations, and 62 decisions.Not here: the private journal (never).Working material — drafts, discards, unsupported claims — is listed below and readable on the working page.Cite: psychedex.org/substances/ketamine/archive

2Build

one panel per compilation run

generation run 2026-04-20

5 min failedmodel not recordedplan not recordedrun/5abad3f7…

research

no artifact

draft

no artifact

audit

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verify

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simplify

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publish

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Selection

results seen0
selected by the model0
consumed as sources48

Verification

claims checked0
supported0
partially supported0
not supported0
inconclusive0
  • record
  • seen / partial
  • working

The model's own caveats

none raised on this run

Reproduce

inputs
48 source keys (listed under Sources)
plan
not recorded — template version, prompt hash and git SHA are written from 2026-09 onward
model
not recorded
streams
none — agent transcripts are persisted from 2026-09 onward

generation run 2026-04-20

74 min completedmodel pipeline-v5plan not recordedrun/1356ee66…

Selection

results seen120
selected by the model52
consumed as sources48

Verification

claims checked199
supported23
partially supported0
not supported1
inconclusive175
  • record
  • seen / partial
  • working

The model's own caveats

  • taper_silent

Reproduce

inputs
48 source keys (listed under Sources)
plan
not recorded — template version, prompt hash and git SHA are written from 2026-09 onward
model
pipeline-v5
streams
none — agent transcripts are persisted from 2026-09 onward
25 searches — query, source, results, what was kept and why
25 searches for this run
#sourcequeryseenkeptrationale
1OpenAlexketamine mechanism action NMDA receptor antagonist pharmacology102Moghaddam 1997 is landmark for glutamate-NMDA-PFC mechanism; Traynelis 2010 is definitive NMDA receptor structure review
2OpenAlexketamine antidepressant treatment-resistant depression rapid83The three landmark ketamine antidepressant papers - essential for clinical history and mechanism
3ClinicalTrials.govketamine treatment depression PTSD104Completed and recruiting RCTs directly relevant to ketamine clinical use
4PubMedketamine bladder uropathy cystitis toxicity105Primary and review papers on ketamine uropathy - chronic toxicity section
5PubMedketamine NMDA receptor binding affinity Ki mechanism of action105Direct Ki binding affinity data for ketamine and metabolites at NMDA, D2 receptors
6PubChemketamine11Primary chemical identity record confirming formula, weight, InChIKey absent from brief
7PubMedketamine antidepressant rapid treatment-resistant depression clinical trial102Esketamine PK/PD review (2026), EQUIVALENCE trial protocol comparing IV ketamine vs IN esketamine
8OpenAlexketamine discovery synthesis history Parke-Davis CI-58151Most comprehensive history of ketamine synthesis and clinical development
9PubMedketamine oral bioavailability norketamine metabolism106Comprehensive PK data across routes of administration
10PubMedketamine opioid receptor sigma receptor binding chiral82Opioid and sigma receptor binding data for pharmacological class verification
11PubMedketamine fatal overdose death toxicology52Fatal overdose data confirming brief's toxicity values
12PubMedketamine neurotoxicity cognitive impairment chronic use21Primate neurotoxicity data for safety section
13PubMedBerman 2000 ketamine antidepressant first RCT11Foundational first RCT of ketamine in depression
14PsychonautWiki—1—Cross-referencing dose data against brief seed values; flags oral threshold discrepancy
15Crossref/DOI10.1038/nature1799811DOI verification confirms journal and authorship
16PubMedZanos 2016 Nature hydroxynorketamine NMDAR-independent11Landmark 2016 Nature paper on HNK mechanism with 1572 citations
17PubMedketamine cognitive memory users psychomotor22Cognitive impairment evidence for chronic neurotoxicity section
18PubMedketamine liver toxicity case105Critical hepatobiliary toxicity evidence for chronic toxicity section
19PubChem REST APICID 3821 SMILES InChIKey properties11SMILES was missing from brief; confirmed via PubChem REST API
20OpenAlexketamine urinary tract uropathy bladder contracted lower urinary symptoms53Uropathy mechanism (Cav1.2), first report citation, comprehensive cystitis review
21PubMedShahani ketamine cystitis ulcerative 200711Confirms Shahani 2007 first case report; indirect citation via Chen 2011
22PubMedesketamine nasal spray SPRAVATO FDA approval depression21Post-marketing safety data for esketamine FDA approval
23PubMedMurrough ketamine midazolam randomized antidepressant 201321Landmark RCT comparing ketamine to active control (midazolam) in TRD
24Multiple web/regulatory sourcesketamine DEA schedule UK class UN convention30Legal status established from Mion 2017 history paper and secondary regulatory knowledge
25PubMedPMID 2702853511Definitive PK review paper confirming metabolism pathways and bioavailability
199 claims by section — every cited sentence, checked against its source
safety70 · 6 ok
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  • Unlike virtually all other general anaesthetics, it preserves upper airway reflexes and spontaneous respiration at anaesthetic concentrations, and produces sympathomimetic-mediated cardiovascular stimulation (increased heart rate and blood pressure) rather than depression.supported

    Clinical toxicology review of ketamine: pharmacological mechanisms, toxic dose ranges, clinical presentations, management. 15563650.2023.2212125

  • Claim in safety — inconclusiveinconclusiveworking →

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  • Direct urothelial apoptosis via nmda-receptor-independent Ca²⁺/mitochondrial pathwaysupported

    Ketamine causes direct urothelial cytotoxicity via mitochondrial stress pathway independent of NMDA receptors. P2Y receptor activation and calcium mobilization implicated in bladder toxicity. j.ajpath.2015.12.014

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  • Lahti et al. (2001) demonstrated dose-related increases in BPRS psychosis and withdrawal subscales in healthy volunteers at 0.1–0.5 mg/kg IV, with effects resolving within 30 minutessupported

    Ketamine produces schizophrenia-like psychotic symptoms in both healthy volunteers and schizophrenic patients; foundational study for NMDA antagonist psychotomimetic effects. pmid:11557159

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  • Opioid receptor engagement may provide an additional reinforcement component.supported

    Ketamine produces opioid system activation in addition to NMDA antagonism. appi.ajp.2018.18020138

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  • Uncontrolled hypertension / severe cardiovascular disease: Ketamine's sympathomimetic effects (increased HR, BP) produce additive cardiovascular stresssupported

    Clinical toxicology review of ketamine: pharmacological mechanisms, toxic dose ranges, clinical presentations, management. 15563650.2023.2212125

  • History of psychosis or schizophrenia: Ketamine exacerbates positive symptoms in schizophrenic patients; 70% experienced symptom worsening in controlled studiessupported

    Ketamine produces schizophrenia-like psychotic symptoms in both healthy volunteers and schizophrenic patients; foundational study for NMDA antagonist psychotomimetic effects. pmid:11557159

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pharmacology33 · 4 ok
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  • At subanesthetic concentrations, NMDA blockade on GABAergic interneurons produces paradoxical disinhibition of glutamate release, increasing prefrontal-cortex glutamate outflow and downstream dopamine release via ampa-receptor/kainate receptor stimulationsupported

    Low doses of ketamine increase glutamate outflow in PFC; AMPA/kainate receptor antagonism blocks ketamine-induced dopamine release and cognitive impairment. jneurosci.17-08-02921.1997

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  • pharmacological/opioid-system activation is required for the acute antidepressant effect: pretreatment with naltrexone abolishes ketamine's antidepressant response without affecting dissociative propertiessupported

    Naltrexone pretreatment blocked antidepressant but not dissociative effects of ketamine. Suggests opioid system activation required for ketamine's antidepressant effect. appi.ajp.2018.18020138

  • Claim in pharmacology — inconclusiveinconclusiveworking →

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  • Primary hepatic metabolism via cyp3a4 and CYP2B6 produces N-demethylation to norketaminesupported

    Metabolism via CYP3A and CYP2B6 to norketamine. s40262-016-0383-6

  • Primary hepatic metabolism via cyp3a4 and CYP2B6 produces N-demethylation to norketaminesupported

    N-demethylation by CYP3A4, CYP2B6, CYP2C9 to norketamine. j.neuropharm.2021.108936

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summary30 · 5 ok
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  • The primary mechanism is noncompetitive, use-dependent blockade of the nmda-receptor ion channel pore (racemic-mixture Ki = 119 nM; S-ketamine Ki = 0.3 µM, approximately 4–5× more potent than the R-enantiomer)supported

    S-ketamine Ki 0.3 uM, R-ketamine Ki 1.4 uM at NMDA receptor. S-enantiomer ~5x more potent than R at NMDA receptor. pmid:9311667

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  • Secondary targets include the dopamine D2High receptor (Ki = 55 nM), mu and kappa opioid receptors, and sigma receptors — all at micromolar affinitiessupported

    Ketamine receptor binding: highest affinity at PCP site. Mu/kappa opioid and sigma receptor binding. pmid:8835358

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  • The antidepressant mechanism involves convergent NMDA blockade-induced synaptogenesis via mTOR and ampa-receptor activation by the (2R,6R)-hydroxynorketamine metabolite, with opioid system engagement required for acute antidepressant response.supported

    Naltrexone pretreatment blocked antidepressant but not dissociative effects of ketamine. Suggests opioid system activation required for ketamine's antidepressant effect. appi.ajp.2018.18020138

  • Acute toxicity is low relative to other anesthetics — ketamine preserves airway reflexes and respiratory drive, and sole-agent fatality is raresupported

    Clinical toxicology review of ketamine: pharmacological mechanisms, toxic dose ranges, clinical presentations, management. 15563650.2023.2212125

  • Chronic toxicity is high: ketamine-induced uropathy (ulcerative cystitis progressing to contracted bladder) is well-documented in regular users, with hepatobiliary damage and prefrontal neurocognitive impairment as additional chronic sequelae. tolerance develops gradually through NMDA receptor upregulation and glutamatergic compensation, with cross-tolerance to other dissociative NMDA antagonists. Psychological dependence liability is high, driven by D2High agonism activating mesolimbic reward circuits and short duration encouraging compulsive redosingsupported

    Systematic review of ketamine-induced uropathy (KIU) in recreational users: clinical presentation, pathophysiology, and treatment. nau.24341

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receptor-pharmacology16 · 3 ok
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  • The S-enantiomer exhibits approximately 4–5× greater potency than the R-enantiomer at NMDA receptors, consistent with its greater clinical potencysupported

    S-ketamine Ki 0.3 uM, R-ketamine Ki 1.4 uM at NMDA receptor. S-enantiomer ~5x more potent than R at NMDA receptor. pmid:9311667

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  • While these affinities are 10–100× weaker than classical opioids, clinical significance has been established: pretreatment with the opioid antagonist naltrexone abolishes ketamine's acute antidepressant effect in treatment-resistant depression without affecting dissociative properties.supported

    Naltrexone pretreatment blocked antidepressant but not dissociative effects of ketamine. Suggests opioid system activation required for ketamine's antidepressant effect. appi.ajp.2018.18020138

  • However, the antidepressant-like effect in forced swim test is not attenuated by sigma antagonists, indicating the in vivo antidepressant mechanism does not primarily depend on sigma receptor activation.supported

    Antidepressant effects in forced swim test not attenuated by sigma antagonists NE-100 or BD1047. j.euroneuro.2011.08.002

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neuroscience12 · 2 ok
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  • This hypothesis explains sustained effects beyond ketamine's pharmacokinetic window but is partially challenged by the Williams et al. (2018) finding that opioid antagonism blocks the acute antidepressant response — HNK does not engage opioid receptors.supported

    Naltrexone pretreatment blocked antidepressant but not dissociative effects of ketamine. appi.ajp.2018.18020138

  • This suggests opioid receptor activation (at micromolar ketamine concentrations) is required for the antidepressant mechanism — potentially through endogenous opioid release secondary to NMDA blockade, or direct ketamine-opioid receptor binding.supported

    Ketamine receptor binding: highest affinity at PCP site. Mu/kappa opioid and sigma receptor binding. pmid:8835358

history10 · 0 ok
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pharmacokinetic-detail10 · 2 ok
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  • Data derived from clinical pharmacokinetic reviews and population PK modelling.supported

    Comprehensive review of ketamine PK/PD. Metabolism via CYP3A and CYP2B6 to norketamine. Oral bioavailability poor due to first-pass metabolism. Nasal administration: rapid Tmax, relatively high bioavailability. s40262-016-0383-6

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  • Primary metabolizing enzymes: cyp3a4 and CYP2B6.supported

    Metabolism via CYP3A and CYP2B6 to norketamine. s40262-016-0383-6

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clinical-evidence8 · 0 ok
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comparative-pharmacology4 · 1 ok
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  • Source: Ebert et al. (1997) and Peltoniemi et al. (2016).supported

    S-ketamine Ki 0.3 uM, R-ketamine Ki 1.4 uM at NMDA receptor. S-norketamine Ki 1.7 uM; R-norketamine 13 uM. pmid:9311667

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legal-status4 · 0 ok
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chemistry2 · 0 ok
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Other runs

  1. brief run2026-09-27completed3 minrun/668e75ad…

3Sources

48 consumed · sorted by year · feeds = sections resting on it

Sources 1 to 30
yearsourcetierstatusfeeds
2026Esketamine Nasal Spray: Mechanism of Action, Clinical, and Translational Sciencevan Hoogdalem MW, Fu DJ, Drevets WC, Zannikos PN · Clinical and Translational Sciencedoi:10.1111/cts.70527strongconsumed1 section
2025Hepatobiliary Complications Associated With Ketamine Use: Clinical Insights and Future DirectionsWaheed HW, Ashraf MR, Sajjad T, et al. · Cureusdoi:10.7759/cureus.84974strongconsumed1 section
2025Ketamine-Induced Cholangiopathy With Concomitant Hemorrhagic CystitisNazir K, Ahmed W, Rafi S, Ahmad A, Khaleeq A · Cureusdoi:10.7759/cureus.99972weakconsumed1 section
2024A Case of Hepatotoxicity Induced by Therapeutic Ketamine Use for SedationYoo N, Thomas S, Bender M, Cheng XJC · Case Reports in Critical Caredoi:10.1155/2024/8366034weakconsumed1 section
2024Real-World Safety of Esketamine Nasal Spray: A Comprehensive Analysis of Esketamine and Respiratory DepressionChepke C, Shelton R, Sanacora G, et al. · International Journal of Neuropsychopharmacologydoi:10.1093/ijnp/pyae058moderateconsumed1 section
2023The clinical toxicology of ketamineSchep LJ, Slaughter RJ, Watts M, Mackenzie E, Gee P · Clinical Toxicologydoi:10.1080/15563650.2023.2212125strongconsumed2 sections
2022CYP 450 enzymes influence (R,S)-ketamine brain delivery and its antidepressant activityNguyen TML, McGowan JC, Gardier AM · Neuropharmacologydoi:10.1016/j.neuropharm.2021.108936strongconsumed1 section
2022Ketamine-Induced Cystitis: A Comprehensive Review of the Urologic Effects of This Psychoactive DrugAnderson DJ, Zhou J, Cao DY, McDonald M, Guenther M · Health Psychology Researchdoi:10.52965/001c.38247strongconsumed1 section
2022Mechanisms of ketamine and its metabolites as antidepressantsHess EM, Riggs LM, Michaelides M, Gould TD · Biochemical Pharmacologydoi:10.1016/j.bcp.2021.114892strongconsumed1 section
2022Norketamine, the Main Metabolite of Ketamine, Induces Mitochondria-Dependent and ER Stress-Triggered Apoptotic Death in Urothelial CellsLin JW, Lin YC, Liu JM, et al. · International Journal of Molecular Sciencesdoi:10.3390/ijms23094666moderateconsumed1 section
2022S-Ketamine Oral Thin Film-Part 1: Population PharmacokineticsSimons P, Olofsen E, van Velzen M, et al. · Frontiers in Pain Researchdoi:10.3389/fpain.2022.946486strongconsumed2 sections
2021Characteristics and circumstances of death related to the self-administration of ketamineDarke S, Duflou J, Farrell M, Peacock A, Lappin J · Addictiondoi:10.1111/add.15154moderateconsumed2 sections
2021Chiral Pharmacokinetics and Metabolite Profile of Prolonged-release Ketamine Tablets in Healthy Human SubjectsHasan M, Modess C, Roustom T, et al. · Anesthesiologydoi:10.1097/aln.0000000000003829strongconsumedcited only
2020Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic MedicationsCosci F, Chouinard G · Psychotherapy and Psychosomaticsdoi:10.1159/000506868strongconsumed2 sections
2020Chronic ketamine abuse is associated with orexin-A reduction and ACTH elevationHuang MC, Chen CH, Chen LY, Chang HM, Chen CK, Lin SK, Xu K · Psychopharmacologydoi:10.1007/s00213-019-05342-9moderateconsumed1 section
2020Disruption of Cav1.2-mediated signaling is a pathway for ketamine-induced pathologyChen H, Vandorpe DH, Xie X, Alper SL, Zeidel ML · Nature Communicationsdoi:10.1038/s41467-020-18167-4moderateconsumed2 sections
2020What urologists need to know about ketamine-induced uropathy: A systematic reviewCastellani D, Pirola GM, Gubbiotti M, Rubilotta E, Gudaru K, Gregori A, Dellabella M · Neurourology and Urodynamicsdoi:10.1002/nau.24341strongconsumed1 section
2018Attenuation of Antidepressant Effects of Ketamine by Opioid Receptor AntagonismWilliams NR, Heifets BD, Blasey C, Sudheimer K, Pannu J, et al. · American Journal of Psychiatrydoi:10.1176/appi.ajp.2018.18020138strongconsumed5 sections
2018Similar psychotic and cognitive profile between ketamine dependence with persistent psychosis and schizophreniaCheng WJ, Chen CH, Chen CK, Huang MC, Pietrzak RH, Krystal JH, Xu K · Schizophrenia Researchdoi:10.1016/j.schres.2018.02.049moderateconsumed1 section
2017History of anaesthesia [Ketamine history editorial]Mion G · European Journal of Anaesthesiologydoi:10.1097/eja.0000000000000638moderateconsumed3 sections
2016Ketamine-Induced Apoptosis in Normal Human Urothelial Cells: A Direct, N-Methyl-d-Aspartate Receptor-Independent Pathway Characterized by Mitochondrial StressBaker SC, Shabir S, Georgopoulos NT, Southgate J · American Journal of Pathologydoi:10.1016/j.ajpath.2015.12.014moderateconsumed1 section
2016Ketamine: 50 Years of Modulating the MindLi L, Vlisides PE · Frontiers in Human Neurosciencedoi:10.3389/fnhum.2016.00612strongconsumed1 section
2016Ketamine: A Review of Clinical Pharmacokinetics and Pharmacodynamics in Anesthesia and Pain TherapyPeltoniemi MA, Hagelberg NM, Olkkola KT, Saari TI · Clinical Pharmacokineticsdoi:10.1007/s40262-016-0383-6strongconsumed4 sections
2016NMDAR inhibition-independent antidepressant actions of ketamine metabolitesZanos P, Moaddel R, Morris PJ, Georgiou P, Fischell J, et al. · Naturedoi:10.1038/nature17998moderateconsumed3 sections
2015Antidepressant-like effects of ketamine, norketamine and dehydronorketamine in forced swim test: Role of activity at NMDA receptorSalat K, Siwek A, Starowicz G, Librowski T, Nowak G, Drabik U, Gajdosz R, Popik P · Neuropharmacologydoi:10.1016/j.neuropharm.2015.07.037moderateconsumed2 sections
2015Population pharmacokinetics of S-ketamine and norketamine in healthy volunteers after intravenous and oral dosingFanta S, Kinnunen M, Backman JT, Kalso E · European Journal of Clinical Pharmacologydoi:10.1007/s00228-015-1826-ystrongconsumedcited only
2015Possible pathophysiology of ketamine-related cystitis and associated treatment strategiesJhang JF, Hsu YH, Kuo HC · International Journal of Urologydoi:10.1111/iju.12841strongconsumed1 section
2014Chronic ketamine exposure induces permanent impairment of brain functions in adolescent cynomolgus monkeysSun L, Li Q, Li Q, Zhang Y, Liu D, Jiang H, Pan F, Yew DT · Addiction Biologydoi:10.1111/adb.12004moderateconsumed2 sections
2014Gender differences in subjective discontinuation symptoms associated with ketamine useChen WY, Huang MC, Lin SK · Substance Abuse Treatment, Prevention, and Policydoi:10.1186/1747-597x-9-39moderateconsumedcited only
2014Plasma brain derived neurotrophic factor (BDNF) and response to ketamine in treatment-resistant depressionHaile CN, Murrough JW, Iosifescu DV, et al. · International Journal of Neuropsychopharmacologydoi:10.1017/s1461145713001119strongconsumedcited only
Show all 49 sources — 19 more
Sources 31 to 49
yearsourcetierstatusfeeds
2013Antidepressant efficacy of ketamine in treatment-resistant major depression: a two-site randomized controlled trialMurrough JW, Iosifescu DV, Chang LC, Al Jurdi RK, et al. · American Journal of Psychiatrydoi:10.1176/appi.ajp.2013.13030392strongconsumed1 section
2013Ketamine Pharmacology: An Update (Pharmacodynamics and Molecular Aspects, Recent Findings)Mion G, Villevieille T · CNS Neuroscience & Therapeuticsdoi:10.1111/cns.12099strongconsumed4 sections
2013Sub-anesthetic concentrations of (R,S)-ketamine metabolites inhibit acetylcholine-evoked currents in α7 nicotinic acetylcholine receptorsMoaddel R, Abdrakhmanova G, Kozak J, et al. · European Journal of Pharmacologydoi:10.1016/j.ejphar.2012.11.023moderateconsumedcited only
2012Evaluation of sigma receptors in the antidepressant-like effects of ketamine in vitro and in vivoRobson MJ, Elliott M, Seminerio MJ, Matsumoto RR · European Neuropsychopharmacologydoi:10.1016/j.euroneuro.2011.08.002moderateconsumed1 section
2012Ketamine-induced biliary dilatation: from Hong Kong to New YorkGutkin E, Hussain SA, Kim SH · Journal of Addiction Medicinedoi:10.1097/adm.0b013e3182399216weakconsumedcited only
2012Rifampicin has a profound effect on the pharmacokinetics of oral S-ketamine and less on intravenous S-ketaminePeltoniemi MA, Saari TI, Hagelberg NM, Laine K, Kurkinen KJ, Neuvonen PJ, Olkkola KT · Basic & Clinical Pharmacology & Toxicologydoi:10.1111/j.1742-7843.2012.00908.xstrongconsumed3 sections
2012Synaptic Dysfunction in Depression: Potential Therapeutic TargetsDuman RS, Aghajanian GK · Sciencedoi:10.1126/science.1222939strongconsumed1 section
2011Drug-induced liver injury following a repeated course of ketamine treatment for chronic pain in CRPS type 1 patients: a report of 3 casesNoppers IM, Niesters M, Aarts LPHJ, et al. · Paindoi:10.1016/j.pain.2011.03.026weakconsumed1 section
2010mTOR-Dependent Synapse Formation Underlies the Rapid Antidepressant Effects of NMDA AntagonistsLi N, Lee B, Liu R, Banasr M, Dwyer JM · Sciencedoi:10.1126/science.1190287moderateconsumed3 sections
2009Is persistent ketamine use a valid model of the cognitive and oculomotor deficits in schizophrenia?Morgan CJ, Huddy V, Lipton M, Curran HV, Joyce EM · Biological Psychiatrydoi:10.1016/j.biopsych.2008.10.045moderateconsumed1 section
2006A randomized trial of an N-methyl-D-aspartate antagonist in treatment-resistant major depressionZarate CA, Singh JB, Carlson PJ, Brutsche NE, Ameli R, Luckenbaugh DA, Charney DS, Manji HK · Archives of General Psychiatrypmid:16894061strongconsumed2 sections
2005Dopamine receptor contribution to the action of PCP, LSD and ketamine psychotomimeticsSeeman P, Ko F, Tallerico T · Molecular Psychiatrypmid:15852061moderateconsumed3 sections
2004Postmortem blood ketamine distribution in two fatalitiesLalonde BR, Wallage HR · Journal of Analytical Toxicologypmid:14987429weakconsumed1 section
2001Effects of ketamine in normal and schizophrenic volunteersLahti AC, Weiler MA, Tamara Michaelidis BA, Parwani A, Tamminga CA · Neuropsychopharmacologypmid:11557159moderateconsumed1 section
2000Antidepressant effects of ketamine in depressed patientsBerman RM, Cappiello A, Anand A, Oren DA, Heninger GR, Charney DS, Krystal JH · Biological Psychiatrypmid:10686270strongconsumed2 sections
1997Activation of Glutamatergic Neurotransmission by Ketamine: A Novel Step in the Pathway from NMDA Receptor Blockade to Dopaminergic and Cognitive DisruptionsMoghaddam B, Adams BW, Verma A, Daly D · Journal of Neurosciencedoi:10.1523/jneurosci.17-08-02921.1997moderateconsumed1 section
1997Norketamine, the main metabolite of ketamine, is a non-competitive NMDA receptor antagonist in the rat cortex and spinal cordEbert B, Mikkelsen S, Thorkildsen C, Borgbjerg FM · European Journal of Pharmacologypmid:9311667moderateconsumed3 sections
1995Interaction of the chiral forms of ketamine with opioid, phencyclidine, sigma and muscarinic receptorsHustveit O, Maurset A, Oye I · Pharmacology & Toxicologypmid:8835358moderateconsumed2 sections
—Oral ketamine may offer a solution to the ketamine conundrumdoi:10.1007/s00213-023-06480-x—unknowncited only

4Docket

one filing per activity — decisions, correspondence, reports

  1. 0012026-04-20revisionRevision 1

    Initial LLM generation (v5 pipeline, wiki)

    psx:substance/ketamine/version/1
  2. 0022026-06-04proposal59 value proposals approved together

    one review action inferred from a shared reviewer and instant — the graph records one activity per proposal

    59 items in this filing

    • dose_tier · light
    • dose_tier · common
    • dose_tier · strong
    • dose_tier · heavy
    • timeline · insufflated · onset
    • timeline · insufflated · come_up
    • timeline · insufflated · peak
    • timeline · insufflated · plateau
    • timeline · insufflated · resolution
    • timeline · insufflated · afterglow
    • timeline · oral · onset
    • timeline · oral · come_up
    • timeline · oral · peak
    • timeline · oral · plateau
    • timeline · oral · resolution
    • timeline · oral · afterglow
    • timeline · intravenous · onset
    • timeline · intravenous · come_up
    • timeline · intravenous · peak
    • timeline · intravenous · resolution
    • timeline · intravenous · afterglow
    • timeline · intramuscular · onset
    • timeline · intramuscular · come_up
    • timeline · intramuscular · peak
    • timeline · intramuscular · resolution
    • timeline · intramuscular · afterglow
    • toxicity
    • dependence · full
    • withdrawal
    • tolerance
    • dosage · insufflated
    • dosage · oral
    • dosage · intramuscular
    • dosage · intravenous
    • duration · insufflated · onset
    • duration · insufflated · peak
    • duration · insufflated · total
    • duration · insufflated · aftereffects
    • duration · oral · onset
    • duration · oral · peak
    • duration · oral · total
    • duration · oral · aftereffects
    • duration · intravenous · onset
    • duration · intravenous · peak
    • duration · intravenous · total
    • duration · intravenous · aftereffects
    • duration · intramuscular · onset
    • duration · intramuscular · peak
    • duration · intramuscular · total
    • duration · intramuscular · aftereffects
    • contraindication · cardiovascular
    • contraindication · cardiovascular
    • contraindication · psychiatric
    • contraindication · hepatic
    • contraindication · renal
    • contraindication · metabolic
    • contraindication · pregnancy_breastfeeding
    • contraindication · respiratory
    psx:substance/ketamine/proposal/dose_tier/5ab91e04-b951-4f4c-bf1d-977d74c755f0
  3. 0032026-06-04publicationPublication — backfill
  4. 0042026-09-27revisionr1.a1

    brief-overview retired 2026-09-30 (founder): Description reads the essential summary for every substance.

    psx:substance/ketamine/version/2

5Issued documents

what the notice, info card and emergency page said, by hash

Issued documents
documentcontent hashissuedfrom versionsuperseded
info_carde8741dbb17a08074456d6848…2026-10-19 20:32Revision 1current
emergencyba304cf8bf8de5b4ec66cb2b…2026-09-04 04:30Revision 1current
info_card09f4d04a4998ad4289c5dd4a…2026-09-04 04:30Revision 1superseded2026-10-19
noticeb144225354d4bad3733c1aa2…2026-09-04 04:30Revision 1current