AOD Thesaurus.  Annotated Hierarchy.  chemical substances by function.  YN - YV14.4
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YNetherapeutic agents   d-out   qh
HN ETOH descriptor 2000.
NT+YPe anti-AOD-abuse agents    qh   ah
+YQ anti-inflammatory, anti-infective, and antineoplastic agents    qh   ah
+YR analgesics and anesthetics    qh   ah
+YS reproductive control agents    qh   ah
+YTe agents used in body system disorders    qh   ah
RT+EBe metabolism    qh   ah
+EB10e drug metabolism    qh   ah
+EE14.4.4.2e therapeutic drug effect    qh   ah

YPeanti-AOD-abuse agents   d-out   qh
SN This section lists pharmacologic agents used in or tested for various facets of the treatment of AOD abuse, its causes, and its consequences. The section begins with a classification of treatment functions that is used throughout, keeping in mind that many of these treatment functions overlap and that many agents are used in multiple functions. The section then is organized by substance or substance class being abused. If the agent being discussed is used in treating abuse of a substance that does not fall into any of the substance classes, use the generic treatment function descriptor combined with the descriptor for the substance.
ST pharmacologic agents for AODD
BT+YNe therapeutic agents    qh   ah
RT+GCe AODD    qh   ah
+HK2.10 AODD drug therapy    qh   ah
YP2.  anti-AOD-abuse agents by function   qh
HN Introduced 1995.
YP2.2e.  .  anti-AOD-intoxication agents   qh
HN Introduced 1995. ETOH descriptor 2000.
NT+YP4.2e anti-alcohol-intoxication agents    qh   ah
 YP6.2 anti-sedative-hypnotic-intoxication agents    qh   ah
 YP10.2 anti-cocaine-intoxication agents    qh   ah
+YP12.2 anti opiate intoxication agents    qh   ah
YP2.4e.  .  AOD detoxification agents   qh
HN Introduced 1995. ETOH descriptor 2000.
NT YP4.4e alcohol detoxification agents    qh   ah
 YP6.4 sedative-hypnotic detoxification agents    qh   ah
+YP8.4 nicotine detoxification agent    qh   ah
 YP10.4 cocaine detoxification agents    qh   ah
+YP12.4 opiate detoxification agents    qh   ah
YP2.6e.  .  AOD withdrawal agents   qh
HN Introduced 1995. ETOH descriptor 2000.
SN Agents for the treatment of acute AOD withdrawal and its symptoms, including substances tested for alleviation of hangover. Protracted withdrawal may cause mental/psychiatric symptoms or lead to the reemergence of preexisting mental disorders that must be treated; see *+YP2.8.12 agents for AOD-concurrent mental disorders* qh ah.
NT+YP4.6e alcohol withdrawal agents    qh   ah
+YP6.6 sedative-hypnotic withdrawal agents    qh   ah
 YP8.6 nicotine withdrawal agents    qh   ah
 YP10.6 cocaine withdrawal agents    qh   ah
+YP12.6 opiate withdrawal agents    qh   ah
YP2.8e.  .  AOD relapse prevention agents   qh
HN Introduced 1995. ETOH descriptor 2000.
ST AOD dependent maintenance agents
NT+YP4.8e alcohol relapse prevention agents    qh   ah
+YP6.8 sedative-hypnotic relapse prevention agents    qh   ah
+YP8.8 nicotine relapse prevention agents    qh   ah
+YP10.8 cocaine relapse prevention agents    qh   ah
+YP12.8 opiate relapse prevention agents    qh   ah
 YW6.2.2e tianeptine    qh   ah
RT+AH20e AODD relapse    qh   ah
YP2.8.2e.  .  .  anti-AOD-craving agents   qh
HN Introduced 1995. ETOH descriptor 2000.
ST anticraving agents
NT+YP4.8.2e anti-alcohol-craving agents    qh   ah
 YP6.8.2 anti-sedative-hypnotic-craving agents    qh   ah
 YP8.8.2 anti-nicotine-craving agents    qh   ah
+YP10.8.2 anti-cocaine-craving agents    qh   ah
 YP12.8.2 anti-opiate-craving agents    qh   ah
YP2.8.4.  .  .  AOD agonist maintenance agents   qh
HN Introduced 1995.
NT YP4.8.4 alcohol agonist maintenance agents    qh   ah
 YP8.8.4 nicotine agonist maintenance agents    qh   ah
 YP10.8.4 cocaine agonist maintenance agents    qh   ah
+YP12.8.4 opiate agonist maintenance agents    qh   ah
YP2.8.6.  .  .  AOD blockers   qh
HN Introduced 1995.
ST AOD antagonists
NT+YP4.8.6e alcohol blockers    qh   ah
 YP6.8.4 sedative-hypnotic blockers    qh   ah
+YP8.8.6 nicotine blockers    qh   ah
+YP10.8.6 cocaine blockers    qh   ah
+YP12.8.6 opiate blockers    qh   ah
YP2.8.8.  .  .  AOD deterrents   qh
HN Introduced 1995.
SN Substances that alter the body's response to an AOD substance, making ingestion of the substance unpleasant or toxic.
ST AOD aversive agents
AOD sensitizing agents
NT+YP4.8.8e alcohol deterrents    qh   ah
 YP6.8.6 sedative-hypnotic deterrents    qh   ah
 YP8.8.8 nicotine deterrents    qh   ah
 YP10.8.8 cocaine deterrents    qh   ah
 YP12.8.8 opiate deterrents    qh   ah
YP2.8.10.  .  .  conditioned AOD aversion agents   qh
HN Introduced 1995.
SN Substances that have unpleasant effects and are given together with an AOD substance.
NT+YP4.8.10e conditioned alcohol aversion agents    qh   ah
YP2.8.12.  .  .  agents for AOD-concurrent mental disorders   qh
HN Introduced 1995.
SN The mental disorder may be primary (i.e., preexisting and underlying AOD abuse) or secondary (i.e., induced by AOD abuse), or symptoms may be caused by or occur with acute and protracted withdrawal. Treatment of these disorders centers mostly on relapse prevention.
ST agents for mental disorder leading to AOD abuse
agents for mental disorder resulting from AOD abuse
NT+YP4.8.12e agents for alcohol-concurrent mental disorders    qh   ah
+YP6.8.8 agents for sedative-hypnotic-concurrent mental disorders    qh   ah
 YP8.8.10 agents for nicotine-concurrent mental disorders    qh   ah
+YP10.8.10 agents for cocaine-concurrent mental disorders    qh   ah
+YP12.8.10 agents for opiate-concurrent mental disorders    qh   ah
RT+YP2.6e AOD withdrawal agents    qh   ah
YP2.8.12.2.  .  .  .  agents for AOD-concurrent depression   qh
HN Introduced 1995.
NT+YP4.8.12.6 agents for alcohol-concurrent depression    qh   ah
 YP6.8.8.2 agents for sedative-hypnotic-concurrent depression    qh   ah
+YP10.8.10.2 agents for cocaine-concurrent depression    qh   ah
 YP12.8.10.2 agents for opiate-concurrent depression    qh   ah
 YW6.2.2e tianeptine    qh   ah
BT+YW6e antidepressants    qh   ah
YP2.8.12.4.  .  .  .  agents for AOD-concurrent anxiety   qh
HN Introduced 1995.
NT+YP4.8.12.8 agents for alcohol-concurrent anxiety    qh   ah
 YP6.8.8.4 agents for sedative-hypnotic-concurrent anxiety    qh   ah
+YP10.8.10.4 agents for cocaine-concurrent anxiety    qh   ah
 YP12.8.10.4 agents for opiate-concurrent anxiety    qh   ah
BT+YW4.10e tranquilizers    qh   ah
YP2.8.12.6.  .  .  .  agents for AOD-related cognitive impairment   qh
HN Introduced 1995.
NT+YP4.8.12.10 agents for alcohol-related cognitive impairment    qh   ah
 YP6.8.8.6 agents for sedative-hypnotic-related cognitive impairment    qh   ah
+YP10.8.10.6 agents for cocaine-related cognitive impairment    qh   ah
 YP12.8.10.6 agents for opiate-related cognitive impairment    qh   ah
YP4e.  anti-alcohol-abuse agents   qh
HN ETOH descriptor 2000.
ST pharmacologic agents for alcoholism treatment
YP4.2e.  .  anti-alcohol-intoxication agents   qh
ST amethystic agents
NT+YH2.4.32e vasopressin    qh   ah
 ZJ2.6.8e ibuprofen    qh   ah
+ZJ2.6.10.4.4.2.2e disulfiram    qh   ah
 ZN2.12e fluvoxamine    qh   ah
 ZQ4.6.4e naloxone    qh   ah
 ZT4.6.6e atipamezole    qh   ah
 ZT6.8.2.2.2.2e daidzin    qh   ah
 ZT6.8.2.2.2.4e puerarin    qh   ah
BT+YP2.2e anti-AOD-intoxication agents    qh   ah
RT+YL2.4 ethanol antagonists    qh   ah
YP4.4e.  .  alcohol detoxification agents   qh
BT+YP2.4e AOD detoxification agents    qh   ah
YP4.6e.  .  alcohol withdrawal agents   qh
SN Agents for the treatment of acute alcohol withdrawal and its symptoms, including substances tested for alleviation of hangover (e.g., pyritinol). Protracted withdrawal may cause mental/psychiatric symptoms or lead to the reemergence of preexisting mental disorders that must be treated; see agents for alcohol concurrent mental disorders.
NT ZA2.4.2.2e lithium    qh   ah
 ZC12.8.10e nitrous oxide    qh   ah
 ZF2.4.2.4 chloral hydrate    qh   ah
 ZF4.2e caroverine    qh   ah
 ZP8.4e bromocriptine    qh   ah
 ZP32.2e apomorphine    qh   ah
 ZT4.6.4e chlormethiazole    qh   ah
 ZT4.14.2e clonidine    qh   ah
+ZT4.26.2.6e dihydropyridine    qh   ah
 ZT4.26.2.10e nifedipine    qh   ah
 ZT4.26.12e pyrithioxin    qh   ah
+ZT4.28.6.6e barbiturates    qh   ah
 ZT4.28.6.6.12e phenobarbital    qh   ah
+ZT8.4.2e carbamazepine    qh   ah
BT+YP2.6e AOD withdrawal agents    qh   ah
RT+YP4.8.2e anti-alcohol-craving agents    qh   ah
+YT8.14e calcium channel blockers    qh   ah
+YV14.2.2e alpha-adrenergic receptor agonists    qh   ah
YP4.6.2e.  .  .  lofexidine   qh
HN ETOH descriptor 2000.
YP4.6.4e.  .  .  slumazenil   qh
HN ETOH descriptor 2000.
YP4.6.6.  .  .  beta blockers for alcohol withdrawal   qh
NT ZN2.16.2.12.4.2e propranolol    qh   ah
 ZN2.16.2.18e atenolol    qh   ah
YP4.6.8e.  .  .  benzodiazepines for alcohol withdrawal   qh
HN ETOH descriptor 2000.
NT ZT6.4.2.2e alprazolam    qh   ah
 ZT6.4.2.8.8e clonazepam    qh   ah
+ZT6.4.2.8.12e diazepam    qh   ah
 ZT6.4.2.8.18e flurazepam    qh   ah
 ZT6.4.2.8.20e lorazepam    qh   ah
 ZT6.4.2.8.24e oxazepam    qh   ah
 ZT6.4.2.8.28e prazepam    qh   ah
 ZT6.4.2.8.30e temazepam    qh   ah
 ZT6.4.2.8.32e halazepam    qh   ah
+ZT6.4.2.10e chlordiazepoxide    qh   ah
 ZT6.4.2.10.2e clorazepate    qh   ah
BT+ZT6.4.2e benzodiazepines    qh   ah
YP4.6.10.  .  .  anti-alcohol-related-delirium agents   qh
NT ZG4.4.2e haloperidol    qh   ah
YP4.6.12.  .  .  anti-alcohol-related-seizures agents   qh
NT ZG8.4.4e valproic acid    qh   ah
 ZT4.14.6.2e phenytoin    qh   ah
 ZT4.28.6.6.12e phenobarbital    qh   ah
+ZT8.4.2e carbamazepine    qh   ah
YP4.8e.  .  alcohol relapse prevention agents   qh
ST alcohol dependent maintenance agents
BT+YP2.8e AOD relapse prevention agents    qh   ah
YP4.8.2e.  .  .  anti-alcohol-craving agents   qh
ST alcohol intake reduction agents
anti-dipsotropic agents
NT YH2.2.2e melatonin    qh   ah
 ZT6.8.2.2.2.2e daidzin    qh   ah
 ZT6.8.2.2.2.4e puerarin    qh   ah
BT+YP2.8.2e anti-AOD-craving agents    qh   ah
RT+YP4.6e alcohol withdrawal agents    qh   ah
YP4.8.2.2e.  .  .  .  serotonergic anti-alcohol-craving agents   qh
HN ETOH descriptor 2000.
NT+YV6.6.2e serotonin uptake inhibitors    qh   ah
 YV6.6.2.2 viqualine    qh   ah
 ZF8.6.2.2.2e sertraline    qh   ah
 ZN2.4.2e fluoxetine    qh   ah
 ZN2.4.4e citalopram    qh   ah
 ZN2.12e fluvoxamine    qh   ah
+ZT4.26.4.2.2e zimelidine    qh   ah
 ZT4.26.4.2.2.2e norzimelidine    qh   ah
 ZT4.28.2e buspirone    qh   ah
YP4.8.2.2.2e.  .  .  .  .  alaproclate   qh
HN ETOH descriptor 2000.
YP4.8.2.2.4e.  .  .  .  .  femoxetine   qh
HN ETOH descriptor 2000.
YP4.8.2.2.6e.  .  .  .  .  indalpine   qh
HN ETOH descriptor 2000.
YP4.8.2.4.  .  .  .  dopaminergic anti-alcohol-craving agents   qh
NT ZP8.4e bromocriptine    qh   ah
YP4.8.2.6.  .  .  .  GABA receptor agonist anti-alcohol-craving agents   qh
NT ZJ2.10.4.2e gamma-hydroxybutyric acid    qh   ah
 ZJ2.10.8.2.2.2.2e calcium acetylhomotaurinate    qh   ah
 ZJ2.10.8.2.2.2.4e bis acetyl homotaurine    qh   ah
YP4.8.2.8.  .  .  .  narcotic antagonist anti-alcohol-craving agents   qh
NT ZQ4.6.4e naloxone    qh   ah
 ZQ4.6.6e naltrexone    qh   ah
 ZQ4.8.6e nalmefene    qh   ah
 ZT4.14.10 ondansetron    qh   ah
YP4.8.2.10.  .  .  .  neuropeptide anti-alcohol-craving agents   qh
NT YH2.4.2e thyrotropin RH    qh   ah
 YH2.4.14e adrenocorticotropic hormone    qh   ah
+YH2.4.32e vasopressin    qh   ah
 YH2.4.36e cholecystokinin    qh   ah
 YV6.6.2.4 amterozide    qh   ah
 ZT4.28.6.4e ritanserin    qh   ah
BT+ZO4.24e neuropeptides    qh   ah
YP4.8.4.  .  .  alcohol agonist maintenance agents   qh
BT+YP2.8.4 AOD agonist maintenance agents    qh   ah
YP4.8.6e.  .  .  alcohol blockers   qh
HN ETOH descriptor 2000.
ST alcohol antagonists
NT ZQ4.6.6e naltrexone    qh   ah
BT+YP2.8.6 AOD blockers    qh   ah
YP4.8.8e.  .  .  alcohol deterrents   qh
HN ETOH descriptor 2000.
SN Substances that alter the body's response to alcohol, making its ingestion unpleasant or toxic.
ST alcohol aversive agents
alcohol sensitizing agents
antidipsotropic agents
NT ZC12.6.2.2e citrated calcium carbimide    qh   ah
+ZJ2.6.10.4.4.2.2e disulfiram    qh   ah
 ZT4.6.8e nitrefazole    qh   ah
BT+YP2.8.8 AOD deterrents    qh   ah
YP4.8.10e.  .  .  conditioned alcohol aversion agents   qh
HN ETOH descriptor 2000.
SN Substances that have unpleasant effects and are given together with alcohol.
NT+ZN2.16.2.10.2e succinylcholine    qh   ah
 ZP32.2e apomorphine    qh   ah
 ZT6.12.2e emetine    qh   ah
BT+YP2.8.10 conditioned AOD aversion agents    qh   ah
YP4.8.12e.  .  .  agents for alcohol-concurrent mental disorders   qh
HN ETOH descriptor 2000.
SN The mental disorder may be primary (i.e., preexisting and underlying alcohol abuse) or secondary (i.e., induced by alcohol abuse), or symptoms may be caused by or occur with acute and protracted withdrawal. Treatment of these disorders centers mostly on relapse prevention.
BT+YP2.8.12 agents for AOD-concurrent mental disorders    qh   ah
YP4.8.12.2.  .  .  .  dopaminergic blockers for alcohol-concurrent mental disorders   qh
NT ZN2.20.6.4e tiapride    qh   ah
 ZT8.14.12e thioridazine    qh   ah
YP4.8.12.4.  .  .  .  dopaminergic agonists for alcohol-concurrent mental disorders   qh
NT ZP8.4e bromocriptine    qh   ah
 ZP32.2e apomorphine    qh   ah
YP4.8.12.6.  .  .  .  agents for alcohol-concurrent depression   qh
NT+YV6.6.2e serotonin uptake inhibitors    qh   ah
+YW6.4e MAO inhibitors    qh   ah
 ZA2.4.2.2e lithium    qh   ah
 ZF8.10.2.2e amitriptyline    qh   ah
 ZN2.4.2e fluoxetine    qh   ah
 ZT8.2.2.4e imipramine    qh   ah
 ZT8.2.2.6e desipramine    qh   ah
 ZT8.8.2e doxepin    qh   ah
BT+YP2.8.12.2 agents for AOD-concurrent depression    qh   ah
+YW6e antidepressants    qh   ah
YP4.8.12.8.  .  .  .  agents for alcohol-concurrent anxiety   qh
NT YW6.4.2 phenelzine    qh   ah
 ZN2.16.2.12.4.2e propranolol    qh   ah
 ZT4.14.2e clonidine    qh   ah
 ZT4.28.2e buspirone    qh   ah
+ZT6.4.2e benzodiazepines    qh   ah
 ZT6.4.2.2e alprazolam    qh   ah
 ZT8.2.2.4e imipramine    qh   ah
BT+YP2.8.12.4 agents for AOD-concurrent anxiety    qh   ah
+YW4.10e tranquilizers    qh   ah
YP4.8.12.10.  .  .  .  agents for alcohol-related cognitive impairment   qh
NT+YV6.6.2e serotonin uptake inhibitors    qh   ah
 ZN2.12e fluvoxamine    qh   ah
 ZT4.14.2e clonidine    qh   ah
BT+YP2.8.12.6 agents for AOD-related cognitive impairment    qh   ah
YP4.8.12.10.2.  .  .  .  .  piridoxilate   qh
YP6.  anti-sedative-hypnotic-abuse agents   qh
SN Agents mentioned here may also apply to alcohol dependence.
YP6.2.  .  anti-sedative-hypnotic-intoxication agents   qh
BT+YP2.2e anti-AOD-intoxication agents    qh   ah
YP6.4.  .  sedative-hypnotic detoxification agents   qh
BT+YP2.4e AOD detoxification agents    qh   ah
YP6.6.  .  sedative-hypnotic withdrawal agents   qh
SN Agents for the treatment of acute sedative-hypnotic withdrawal. Protracted withdrawal may cause mental/psychiatric symptoms that must be treated, see *+YP6.8.8 agents for sedative-hypnotic-concurrent mental disorders* qh ah.
BT+YP2.6e AOD withdrawal agents    qh   ah
YP6.6.2.  .  .  barbiturate withdrawal agents   qh
NT ZT4.28.6.6.10e pentobarbital    qh   ah
 ZT4.28.6.6.12e phenobarbital    qh   ah
YP6.6.4.  .  .  benzodiazepine withdrawal agents   qh
NT+ZT6.4.2.8.12e diazepam    qh   ah
YP6.8.  .  sedative-hypnotic relapse prevention agents   qh
ST sedative-hypnotic dependent maintenance agents
BT+YP2.8e AOD relapse prevention agents    qh   ah
YP6.8.2.  .  .  anti-sedative-hypnotic-craving agents   qh
ST sedative-hypnotic intake reduction agents
BT+YP2.8.2e anti-AOD-craving agents    qh   ah
YP6.8.4.  .  .  sedative-hypnotic blockers   qh
SN Agents that block the mood-altering or analgesic effects of sedative-hypnotics.
BT+YP2.8.6 AOD blockers    qh   ah
YP6.8.6.  .  .  sedative-hypnotic deterrents   qh
BT+YP2.8.8 AOD deterrents    qh   ah
YP6.8.8.  .  .  agents for sedative-hypnotic-concurrent mental disorders   qh
SN The mental disorder may be primary (i.e., preexisting and underlying sedative-hypnotic abuse) or secondary (i.e., induced by sedative-hypnotic abuse), or symptoms may be caused by or occur with acute and protracted withdrawal. Treatment of these disorders centers mostly on relapse prevention.
BT+YP2.8.12 agents for AOD-concurrent mental disorders    qh   ah
YP6.8.8.2.  .  .  .  agents for sedative-hypnotic-concurrent depression   qh
BT+YP2.8.12.2 agents for AOD-concurrent depression    qh   ah
+YW6e antidepressants    qh   ah
YP6.8.8.4.  .  .  .  agents for sedative-hypnotic-concurrent anxiety   qh
BT+YP2.8.12.4 agents for AOD-concurrent anxiety    qh   ah
+YW4.10e tranquilizers    qh   ah
YP6.8.8.6.  .  .  .  agents for sedative-hypnotic-related cognitive impairment   qh
BT+YP2.8.12.6 agents for AOD-related cognitive impairment    qh   ah
YP8.  anti-nicotine-abuse agents   qh
NT ZT4.14.2e clonidine    qh   ah
YP8.2.  .  busprione   qh
YP8.4.  .  nicotine detoxification agent   qh
ST nicotine substitution agents
BT+YP2.4e AOD detoxification agents    qh   ah
YP8.4.2.  .  .  nicotin gum   qh
YP8.6.  .  nicotine withdrawal agents   qh
SN Agents for the treatment of acute nicotine withdrawal. Protracted withdrawal may cause mental/psychiatric symptoms that must be treated; see agents for nicotine concurrent mental disorders.
BT+YP2.6e AOD withdrawal agents    qh   ah
RT YP8.8.2 anti-nicotine-craving agents    qh   ah
YP8.8.  .  nicotine relapse prevention agents   qh
ST nicotine dependent maintenance agents
BT+YP2.8e AOD relapse prevention agents    qh   ah
YP8.8.2.  .  .  anti-nicotine-craving agents   qh
ST nicotine intake reduction agents
BT+YP2.8.2e anti-AOD-craving agents    qh   ah
RT YP8.6 nicotine withdrawal agents    qh   ah
YP8.8.4.  .  .  nicotine agonist maintenance agents   qh
BT+YP2.8.4 AOD agonist maintenance agents    qh   ah
YP8.8.6.  .  .  nicotine blockers   qh
SN Agents that block the mood-altering or analgesic effects of nicotine.
ST nicotine antagonist maintenance agents
NT ZU6.2e mecamylamine    qh   ah
BT+YP2.8.6 AOD blockers    qh   ah
YP8.8.8.  .  .  nicotine deterrents   qh
ST nicotine aversive agents
BT+YP2.8.8 AOD deterrents    qh   ah
YP8.8.10.  .  .  agents for nicotine-concurrent mental disorders   qh
SN The mental disorder may be primary (i.e., preexisting and underlying nicotine abuse) or secondary (i.e., induced by nicotine abuse), or symptoms may be caused by or occur with acute and protracted withdrawal. Treatment of these disorders centers mostly on relapse prevention.
BT+YP2.8.12 agents for AOD-concurrent mental disorders    qh   ah
YP10.  anti-cocaine-abuse agents   qh
YP10.2.  .  anti-cocaine-intoxication agents   qh
BT+YP2.2e anti-AOD-intoxication agents    qh   ah
YP10.4.  .  cocaine detoxification agents   qh
BT+YP2.4e AOD detoxification agents    qh   ah
YP10.6.  .  cocaine withdrawal agents   qh
SN Agents for the treatment of acute cocaine withdrawal. Protracted withdrawal may cause mental/psychiatric symptoms that must be treated; see agents for cocaine concurrent mental disorders.
BT+YP2.6e AOD withdrawal agents    qh   ah
RT+YP10.8.2 anti-cocaine-craving agents    qh   ah
YP10.8.  .  cocaine relapse prevention agents   qh
ST cocaine dependent maintenance agents
NT ZQ6.2e buprenorphine    qh   ah
+ZT8.4.2e carbamazepine    qh   ah
 ZT8.16.2.2e flupenthixol    qh   ah
BT+YP2.8e AOD relapse prevention agents    qh   ah
YP10.8.2.  .  .  anti-cocaine-craving agents   qh
NT ZF8.2 amantadine    qh   ah
+ZO2e amino acids    qh   ah
 ZO2.2.2.14e tryptophan    qh   ah
 ZO2.2.4.10e tyrosine    qh   ah
 ZT6.4.2.6e carbamazepin    qh   ah
 ZT8.2.2.6e desipramine    qh   ah
 ZT8.16.2.2e flupenthixol    qh   ah
BT+YP2.8.2e anti-AOD-craving agents    qh   ah
RT YP10.6 cocaine withdrawal agents    qh   ah
YP10.8.2.2.  .  .  .  bupropion   qh
YP10.8.4.  .  .  cocaine agonist maintenance agents   qh
BT+YP2.8.4 AOD agonist maintenance agents    qh   ah
YP10.8.6.  .  .  cocaine blockers   qh
SN Agents that block the mood-altering or analgesic effects of cocaine.
ST cocaine antagonist maintenance agents
NT ZG4.4.2e haloperidol    qh   ah
 ZP8.4e bromocriptine    qh   ah
 ZT4.18.4e trazodone    qh   ah
 ZT8.2.2.4e imipramine    qh   ah
BT+YP2.8.6 AOD blockers    qh   ah
RT+YV6 neuroregulator blockaders    qh   ah
YP10.8.8.  .  .  cocaine deterrents   qh
ST cocaine aversive agents
BT+YP2.8.8 AOD deterrents    qh   ah
YP10.8.10.  .  .  agents for cocaine-concurrent mental disorders   qh
SN The mental disorder may be primary (i.e., preexisting and underlying cocaine abuse) or secondary (i.e., induced by cocaine abuse), or symptoms may be caused by or occur with acute and protracted withdrawal. Treatment of these disorders centers mostly on relapse prevention.
NT ZJ2.4e methylphenydate    qh   ah
 ZT4.16.4.2e magnesium pemoline    qh   ah
BT+YP2.8.12 agents for AOD-concurrent mental disorders    qh   ah
YP10.8.10.2.  .  .  .  agents for cocaine-concurrent depression   qh
NT ZF8.4 maprotiline    qh   ah
 ZT4.18.4e trazodone    qh   ah
 ZT8.2.2.4e imipramine    qh   ah
 ZT8.2.2.6e desipramine    qh   ah
 ZT8.8.2e doxepin    qh   ah
BT+YP2.8.12.2 agents for AOD-concurrent depression    qh   ah
+YW6e antidepressants    qh   ah
YP10.8.10.4.  .  .  .  agents for cocaine-concurrent anxiety   qh
NT ZT8.2.2.6e desipramine    qh   ah
BT+YP2.8.12.4 agents for AOD-concurrent anxiety    qh   ah
+YW4.10e tranquilizers    qh   ah
YP10.8.10.6.  .  .  .  agents for cocaine-related cognitive impairment   qh
SN *GZ12.2.2 attention deficit disorder with hyperactivity* qh ah in particular is associated with cocaine abuse.
NT ZJ2.10.4.8e methylphenidate    qh   ah
 ZT4.16.4.2e magnesium pemoline    qh   ah
BT+YP2.8.12.6 agents for AOD-related cognitive impairment    qh   ah
YP12.  anti-opiate-abuse agents   qh
YP12.2.  .  anti opiate intoxication agents   qh
NT ZQ4.6.4e naloxone    qh   ah
BT+YP2.2e anti-AOD-intoxication agents    qh   ah
YP12.4.  .  opiate detoxification agents   qh
NT ZQ4.6.6e naltrexone    qh   ah
+ZQ10.2e methadone    qh   ah
 ZT4.14.2e clonidine    qh   ah
BT+YP2.4e AOD detoxification agents    qh   ah
YP12.6.  .  opiate withdrawal agents   qh
SN Agents for the treatment of acute opiate withdrawal. Protracted withdrawal may cause mental/psychiatric symptoms that must be treated; see agents for opiate concurrent mental disorders.
NT+ZQ10.2e methadone    qh   ah
 ZT4.14.2e clonidine    qh   ah
BT+YP2.6e AOD withdrawal agents    qh   ah
RT YP12.8.2 anti-opiate-craving agents    qh   ah
YP12.8.  .  opiate relapse prevention agents   qh
ST opiate dependent maintenance agents
BT+YP2.8e AOD relapse prevention agents    qh   ah
YP12.8.2.  .  .  anti-opiate-craving agents   qh
ST opiate intake reduction agents
BT+YP2.8.2e anti-AOD-craving agents    qh   ah
RT+YP12.6 opiate withdrawal agents    qh   ah
+YP12.8.4 opiate agonist maintenance agents    qh   ah
+YP12.8.6 opiate blockers    qh   ah
YP12.8.4.  .  .  opiate agonist maintenance agents   qh
NT ZQ6.2e buprenorphine    qh   ah
+ZQ10.2e methadone    qh   ah
 ZQ10.4e LAAM    qh   ah
BT+YP2.8.4 AOD agonist maintenance agents    qh   ah
RT YP12.8.2 anti-opiate-craving agents    qh   ah
YP12.8.6.  .  .  opiate blockers   qh
SN Agents that block the mood-altering or analgesic effects of opiates.
ST opiate antagonist maintenance agents
NT ZQ4.6.6e naltrexone    qh   ah
BT+YP2.8.6 AOD blockers    qh   ah
RT YP12.8.2 anti-opiate-craving agents    qh   ah
YP12.8.8.  .  .  opiate deterrents   qh
BT+YP2.8.8 AOD deterrents    qh   ah
YP12.8.10.  .  .  agents for opiate-concurrent mental disorders   qh
SN The mental disorder may be primary (i.e., preexisting and underlying opiate abuse) or secondary (i.e., induced by opiate abuse), or symptoms may be caused by or occur with acute and protracted withdrawal. Treatment of these disorders centers mostly on relapse prevention.
BT+YP2.8.12 agents for AOD-concurrent mental disorders    qh   ah
YP12.8.10.2.  .  .  .  agents for opiate-concurrent depression   qh
BT+YP2.8.12.2 agents for AOD-concurrent depression    qh   ah
+YW6e antidepressants    qh   ah
YP12.8.10.4.  .  .  .  agents for opiate-concurrent anxiety   qh
BT+YP2.8.12.4 agents for AOD-concurrent anxiety    qh   ah
+YW4.10e tranquilizers    qh   ah
YP12.8.10.6.  .  .  .  agents for opiate-related cognitive impairment   qh
BT+YP2.8.12.6 agents for AOD-related cognitive impairment    qh   ah

YQanti-inflammatory, anti-infective, and antineoplastic agents   d-out   qh
BT+YNe therapeutic agents    qh   ah
YQ2e.  anti-inflammatory agents   qh
ST tissue protective agents
tissue repair agents
NT ZN2.18.2.2.2.2.2e R alpha methylhistamine    qh   ah
YQ2.2.  .  nonsteroidal anti-inflammatory drugs   qh
ST NSAID
NT+YR2.2.6 gout suppressants    qh   ah
+ZJ2.10.10.2.4.2.4e salicylate    qh   ah
 ZT4.24.4e antipyrine    qh   ah
 ZT4.30.12e tolmetin    qh   ah
 ZT4.34.2e piroxicam    qh   ah
 ZT6.10.6e indomethacin    qh   ah
YQ2.4.  .  steroidal anti-inflammatory drugs   qh
NT YH4.6.2.2e dexamethasone    qh   ah
 ZV8.2.2.2e prednisone    qh   ah
 ZV8.2.4.2e prednisolone    qh   ah
RT+ZVe steroids    qh   ah
YQ4e.  anti-infective agents   qh
NT+YT12.2 urinary anti-infective agents    qh   ah
+ZN2.20.8e sulfonamide    qh   ah
YQ4.2.  .  local anti-infective agents   qh
NT ZJ2.6.10.4.4.4.2e thiram    qh   ah
YQ4.4.  .  antitubercular agents   qh
NT ZF6.6e isoniazid    qh   ah
RT+GH16.14.4.2e tuberculosis    qh   ah
YQ4.6.  .  antibacterial agents   qh
NT ZT6.24.2e ciprofloxacin    qh   ah
YQ4.6.2.  .  .  leprostatic agents   qh
NT YQ4.14.16.2 rifampin    qh   ah
 ZJ2.10.10.6.2.2e thalidomide    qh   ah
RT GH16.14.4.4 Hansen's disease    qh   ah
YQ4.8.  .  antifungal agents   qh
NT+YQ4.14.6 antifungal antibiotics    qh   ah
 ZJ2.6.10.4.4.4.2e thiram    qh   ah
YQ4.10.  .  antiparasitic agents   qh
NT ZT4.32.4e kainate    qh   ah
YQ4.10.2.  .  .  anthelmintics   qh
YQ4.10.4.  .  .  antiprotozoal agents   qh
YQ4.10.4.2.  .  .  .  antimalarials   qh
NT ZP4.4e quinine    qh   ah
 ZT4.28.4e pyrimethamine    qh   ah
 ZT8.2.2.2e quinacrine    qh   ah
YQ4.12.  .  antiviral agents   qh
NT YE10.8.4e interferon    qh   ah
YQ4.12.2.  .  .  acyclovir   qh
YQ4.14e.  .  antibiotics   qh
NT YD8.12.2e ionophores    qh   ah
 ZF2.4.2.8.2e chloramphenicol    qh   ah
YQ4.14.2.  .  .  aminoglycoside antibiotics   qh
NT+ZG8.2.2.2e gentamicin    qh   ah
 ZG8.2.2.4e neomycin    qh   ah
YQ4.14.4.  .  .  antitubercular antibiotics   qh
NT YQ4.14.16.2 rifampin    qh   ah
YQ4.14.6.  .  .  antifungal antibiotics   qh
NT ZT4.20.8.2e cycloheximide    qh   ah
BT+YQ4.8 antifungal agents    qh   ah
YQ4.14.6.2.  .  .  .  griseofulvin   qh
BT+YD8.2 ADH antagonists    qh   ah
YQ4.14.6.4.  .  .  .  nystatin   qh
YQ4.14.8.  .  .  antineoplastic antibiotics   qh
BT+YQ6 antineoplastic agents    qh   ah
YQ4.14.10.  .  .  lactam antibiotics   qh
YQ4.14.10.2.  .  .  .  moxalactam   qh
YQ4.14.10.4.  .  .  .  penicillin   qh
YQ4.14.10.4.2.  .  .  .  .  penicillin G   qh
ST penicillin G benzathine
penicillin G procaine
YQ4.14.12.  .  .  macrolide antibiotics   qh
YQ4.14.12.2.  .  .  .  amphotericin   qh
YQ4.14.12.4.  .  .  .  erythromycin   qh
YQ4.14.14.  .  .  bacitracin   qh
YQ4.14.16.  .  .  rifamycins   qh
YQ4.14.16.2.  .  .  .  rifampin   qh
BT+YQ4.6.2 leprostatic agents    qh   ah
+YQ4.14.4 antitubercular antibiotics    qh   ah
YQ4.14.18e.  .  .  tetracyclines   qh
HN ETOH descriptor 2000.
YQ4.14.20.  .  .  combined antibiotics   qh
YQ6.  antineoplastic agents   qh
ST anti-neoplastic agents
NT YQ4.14.8 antineoplastic antibiotics    qh   ah
 ZJ2.6.10.4.6e urethane    qh   ah
 ZN2.20.6.8e procarbazine    qh   ah
 ZT8.2.2.2e quinacrine    qh   ah
 ZV8.2.2.2e prednisone    qh   ah
RT YE12e immunosuppressive agents    qh   ah

YRanalgesics and anesthetics   d-out   qh
HN Introduced 1995.
BT+YNe therapeutic agents    qh   ah
YR2e.  analgesics   qh
SN Substances that reduce pain and that may or may not have other psychoactive properties. See *+ZQ opioids* qh ah.
      Drugs that relieve pain without blocking the conduction of nerve impulses or markedly altering the function of the sensory apparatus. The narcotic analgesics act on the central nervous system, produce dependence, and alter the patient's perception; they are primarily used for severe pain. The nonnarcotic analgesics act at the site of pain, do not produce dependence, and do not alter the patient's perception; they are used for mild to moderate pain.
NT+YW4.2e narcotic analgesics    qh   ah
 ZJ2.10.10.4.2e tilidine    qh   ah
RT GC2.6 abuse of non-dependence-producing substance    qh   ah
+HU2e analgesia    qh   ah
YR2.2.  .  nonnarcotic analgesics   qh
SN The nonnarcotic analgesics act at the site of pain, do not produce dependence, and do not alter the patient's perception; they are used for mild to moderate pain.
ST anti-inflammatory analgesics
non-opioid analgesics
NT+ZJ2.10.10.2.4.2.4e salicylate    qh   ah
 ZT4.24.4e antipyrine    qh   ah
 ZT4.30.12e tolmetin    qh   ah
 ZT4.34.2e piroxicam    qh   ah
YR2.2.2.  .  .  prescription nonnarcotic analgesics   qh
HN Introduced 1995.
YR2.2.4.  .  .  non-prescription nonnarcotic analgesics   qh
HN Introduced 1995.
YR2.2.6.  .  .  gout suppressants   qh
NT ZN2.20.2.2.6e phenacetin    qh   ah
 ZP6e colchicine    qh   ah
 ZT6.10.6e indomethacin    qh   ah
BT+YQ2.2 nonsteroidal anti-inflammatory drugs    qh   ah
YR2.2.6.2.  .  .  .  uricosuric agents   qh
YR4e.  anesthetics   qh
HN ETOH descriptor 2000.
SN Agents that produce a local or general loss of sensation, including pain. Local anesthesia involves loss of sensation in one area of the body by blockage of conduction in nerves. General anesthesia involves loss of consciousness, usually for the purpose of relieving pain during surgery.
NT+YW4.4e general anesthetics    qh   ah
 ZC12.8.10e nitrous oxide    qh   ah
 ZF4.4e propofol    qh   ah
 ZJ2.6.10.2.4.2e sodium oxybate    qh   ah
 ZL2.6.4e chloroform    qh   ah
 ZL2.6.8e trichloroethylene    qh   ah
+ZT4.28.6.6e barbiturates    qh   ah
RT+HU4e anesthesia    qh   ah
+YW4.4e general anesthetics    qh   ah
YR4.2e.  .  local anesthetics   qh
HN ETOH descriptor 2000.
SN Agents that block conduction in nerve axons in the peripheral nervous system when applied locally to nerve tissue.
ST anesthetic, local
NT+BK2e cocaine    qh   ah
 ZJ2.10.10.2.2.2.4e procaine    qh   ah

YSreproductive control agents   d-out   qh
ST contraceptive agents
NT ZK4.4.8.6.2e misoprostol    qh   ah
BT+YNe therapeutic agents    qh   ah
RT HS4.2e contraception    qh   ah
YS2e.  female contraceptive agents   qh
ST birth control pills
NT ZV6.2e mifepristone    qh   ah
RT+YH4.10.4 synthetic progestational hormones    qh   ah
+ZV22e synthetic steroids    qh   ah
YS4e.  male contraceptive agents   qh

YTeagents used in body system disorders   d-out   qh
NT+YV peripheral nervous system agents    qh   ah
BT+YNe therapeutic agents    qh   ah
YT2e.  appetite suppressants   qh
SN Agents used to reduce hunger and diminish food intake in the treatment of obesity.
      Also called anorexiants or anorectic agents. Most of these drugs are sympathomimetic amines, whose efficacy is limited by associated insomnia, dependence phenomena, and other adverse effects. Amphetamines formerly were used for their appetite-suppressing effects.
ST anorectic agents
anorexiants
appetite depressants
NT+BJ2.2e amphetamines    qh   ah
+ZN2.10.2e fenfluramine    qh   ah
YT4.  antimetabolites   qh
NT ZT4.26.10.4e pyrithiamine    qh   ah
+ZT4.28.6.8.2e thiouracil    qh   ah
 ZT4.28.6.8.2.2e propylthiouracil    qh   ah
YT6e.  neuromuscular agents   qh
HN ETOH descriptor 2000.
YT6.2.  .  central muscle relaxants   qh
NT ZJ2.6.10.4.2e meprobamate    qh   ah
 ZT6.4.2.8.28e prazepam    qh   ah
YT6.4.  .  neuromuscular blocking agents   qh
YT6.4.2.  .  .  curare   qh
RT+ZPe alkaloids    qh   ah
YT6.6.  .  neuromuscular depolarizing agents   qh
NT+ZN2.16.2.10.2e succinylcholine    qh   ah
YT8e.  cardiovascular agents   qh
YT8.2.  .  antiarrhythmia agents   qh
NT ZJ2.10.10.2.2.2.2e procainamide    qh   ah
 ZN2.16.2.12.4.2e propranolol    qh   ah
 ZP4.2e quinidine    qh   ah
 ZP20e sparteine    qh   ah
 ZT4.14.6.2e phenytoin    qh   ah
RT+YT8.6e vasodilator agents    qh   ah
YT8.4e.  .  vasoconstrictor agents   qh
HN Introduced 1995.
ST vasopressor agents
NT+YH2.4.6e angiotensin    qh   ah
+YH2.4.32e vasopressin    qh   ah
+YT8.12e calcium channel agonists    qh   ah
 ZN2.16.2.4e phenylephrine    qh   ah
 ZN2.16.2.20e methoxamine    qh   ah
RT EL4.10e vasoconstriction    qh   ah
YT8.6e.  .  vasodilator agents   qh
HN ETOH descriptor 1995.
NT BC4 theophylline    qh   ah
+YT8.14e calcium channel blockers    qh   ah
 ZC12.6.4.2e sodium nitroprusside    qh   ah
 ZC12.8.6.2e amyl nitrite    qh   ah
 ZC12.8.6.4e butyl nitrite    qh   ah
 ZF2.2.4.2e ifenprodil    qh   ah
 ZF2.12.2.2e nitroglycerin    qh   ah
 ZF2.12.8.2.2e isosorbide dinitrate    qh   ah
 ZF4.6e resveratrol    qh   ah
 ZN2.16.2.12.4.2e propranolol    qh   ah
 ZN2.16.2.16e suloctidil    qh   ah
RT+YT8.2 antiarrhythmia agents    qh   ah
YT8.8.  .  antihypertensive agents   qh
ST hypertensive medication
NT ZC12.6.4.2e sodium nitroprusside    qh   ah
 ZN2.10.6e phenoxybenzamine    qh   ah
 ZN2.16.2.12.4.2e propranolol    qh   ah
 ZO2.2.8.6.2e captopril    qh   ah
 ZP18.4.4e nimodipine    qh   ah
+ZP26e rauwolfia alkaloids    qh   ah
 ZT4.14.2e clonidine    qh   ah
 ZT4.14.12e phentolamine    qh   ah
 ZT4.26.2.6.4e isradipine    qh   ah
 ZT4.26.2.6.6e nitrendipine    qh   ah
 ZT6.20.6e prazosin    qh   ah
YT8.10.  .  cardiotonic agents   qh
NT+YH2.2.6.6e norepinephrine    qh   ah
+ZG8.2.6e cardiac glycosides    qh   ah
 ZN2.16.2.4e phenylephrine    qh   ah
YT8.12e.  .  calcium channel agonists   qh
HN Introduced 1995. ETOH descriptor 2000.
NT ZT4.26.2.6.2e Bay K 8644    qh   ah
BT+YT8.4e vasoconstrictor agents    qh   ah
YT8.14e.  .  calcium channel blockers   qh
NT ZF4.2e caroverine    qh   ah
 ZM4e verapamil    qh   ah
 ZP18.4.4e nimodipine    qh   ah
 ZT4.20.6e perhexiline    qh   ah
 ZT4.26.2.6.4e isradipine    qh   ah
 ZT4.26.2.6.6e nitrendipine    qh   ah
 ZT4.26.2.10e nifedipine    qh   ah
BT+YT8.6e vasodilator agents    qh   ah
RT+YP4.6e alcohol withdrawal agents    qh   ah
YT10e.  gastrointestinal agents   qh
NT YC4.10.4.2e pepsin    qh   ah
+YG6 gastrointestinal hormones    qh   ah
YT10.2e.  .  emetic agents   qh
HN Changed descriptor 2000; through 1999 use "emetics." ETOH descriptor 2000.
SN Agent that causes vomiting.
ST emetics
BT+YV6 neuroregulator blockaders    qh   ah
YT10.2.2.  .  .  ipecac   qh
BT+ZPe alkaloids    qh   ah
RT+HK2.12.2e chemical aversion therapy    qh   ah
YT10.4.  .  laxatives   qh
RT BN other specific drug of abuse    qh   ah
YT10.6.  .  antidiarrheals   qh
NT ZH10e pectin    qh   ah
YT10.8.  .  antiulcer agents   qh
NT ZH8.4.2.2e sucralfate    qh   ah
 ZK4.4.8.6.2e misoprostol    qh   ah
 ZT4.12.4e ranitidine    qh   ah
 ZT4.36.2e famotidine    qh   ah
 ZT4.38e cimetidine    qh   ah
 ZT6.4.2.8.34e omeprazole    qh   ah
YT10.10e.  .  bile acids and salts   qh
NT EB26e bile acid metabolism    qh   ah
+ZV10.2e cholic acid    qh   ah
 ZV10.2.2.2e chenodeoxycholic acid    qh   ah
RT XM6.6e bile    qh   ah
+ZV10e cholanes    qh   ah
YT10.12.  .  cathartics   qh
YT10.14.  .  antisecretory agents   qh
ST antisecretory drugs
NT ZT4.12.4e ranitidine    qh   ah
 ZT4.38e cimetidine    qh   ah
 ZT6.4.2.8.34e omeprazole    qh   ah
YT12e.  urinary system agents   qh
YT12.2.  .  urinary anti-infective agents   qh
NT+ZT4.12.2e nitrofuran    qh   ah
BT+YQ4e anti-infective agents    qh   ah
YT12.4.  .  renal agents   qh
YT12.4.2e.  .  .  diuretics   qh
HN ETOH descriptor 1995.
NT YG34.2.2 spironolactone    qh   ah
YT14e.  hematologic agents   qh
YT14.2e.  .  anticoagulants   qh
ST anticoagulant drugs
NT ZO6.8.12.12e protein C    qh   ah
RT EE16.6e antagonistic drug interaction    qh   ah
YT14.4e.  .  coagulants   qh
RT+ZO6.4.10.6.4e blood coagulation factors    qh   ah
YT14.6.  .  platelet aggregation inhibitors   qh
HN Introduced 1995.
NT ZJ2.10.10.2.4.2.2e acetylsalicylic acid    qh   ah
 ZK4.4.8.2e prostacyclin    qh   ah
 ZT6.20.2e ketanserin    qh   ah
YT14.6.2.  .  .  hemostatics   qh
NT YC4.10.4.8.4e thrombin    qh   ah
YT14.6.4.  .  .  heparin antagonists   qh
NT YB18e vitamin K    qh   ah
RT EE16.6e antagonistic drug interaction    qh   ah
YT14.8e.  .  fibrinolytic agents   qh
HN ETOH descriptor 2000.
ST antithrombotic agents
NT YC4.10.4.4e plasminogen activator    qh   ah
 YC4.10.4.8.12 streptokinase    qh   ah
 YC18.2e plasminogen    qh   ah
YT14.10.  .  hematinics   qh
NT+YB12.24e vitamin B12    qh   ah
YT14.12.  .  plasma substitutes   qh
NT ZH10e pectin    qh   ah
YV.  peripheral nervous system agents   d-out   qh
HN Introduced 1995.
SN Many of these agents also have secondary effects on the central nervous system.
BT+YTe agents used in body system disorders    qh   ah
YV2.  .  bronchodilator agents   qh
ST bronchodilators
NT BC4 theophylline    qh   ah
+YH2.2.6e epinephrine    qh   ah
 ZN2.16.2.4e phenylephrine    qh   ah
YV4.  .  neuroregulators   qh
NT+YH2.2.6e epinephrine    qh   ah
+YH2.2.6.6e norepinephrine    qh   ah
 YH2.4.36e cholecystokinin    qh   ah
+ZJ2.6.10.2.2e aminobutyric acid    qh   ah
+ZN2.18.2e acetylcholine    qh   ah
+ZO4.24e neuropeptides    qh   ah
 ZO4.24.4.4.2e substance P    qh   ah
+ZQ20.2e endorphins    qh   ah
 ZT6.10.12.4e serotonin    qh   ah
RT+YJ2e neurotransmitters    qh   ah
YV4.2.  .  .  dopaminergic agents   qh
NT+ZN2.8.4e dopa    qh   ah
+ZN2.8.6e dopamine    qh   ah
 ZP32.2e apomorphine    qh   ah
 ZT6.12.6e nomifensine    qh   ah
YV6.  .  neuroregulator blockaders   qh
ST neuroregulator blockers
NT+YT10.2e emetic agents    qh   ah
RT+YP10.8.6 cocaine blockers    qh   ah
YV6.2.  .  .  antiemetics   qh
ST anti-emetic agents
NT ZT8.14.10e promethazine    qh   ah
YV6.4e.  .  .  histamine antagonists   qh
RT EE16.6e antagonistic drug interaction    qh   ah
YV6.4.2e.  .  .  .  histamine H1 receptor blockaders   qh
SN A group of therapeutic drugs used in the treatment of allergic disorders (and sometimes, because of their mild sedating effects, to allay anxiety and induce sleep). Usually they are abused with codeine or alcohol because they act synergistically to magnify the sedative effects of both.
ST antihistamines
antihistaminics
H1 blockers
NT ZT4.26.2.2e pyrilamine    qh   ah
 ZT4.26.2.4e tripelennamine    qh   ah
 ZT8.14.10e promethazine    qh   ah
BT+YW4.8e sedative-hypnotics    qh   ah
RT+YW4.8.4e nonbarbiturate sedative-hypnotics    qh   ah
YV6.4.4e.  .  .  .  histamine H2 receptor blockaders   qh
ST H2 blockers
NT ZT4.12.4e ranitidine    qh   ah
 ZT4.36.2e famotidine    qh   ah
 ZT4.38e cimetidine    qh   ah
YV6.6e.  .  .  serotonin antagonists   qh
SN Drugs that bind to but do not activate serotonin receptors, thereby blocking the actions of serotonin or serotonin agonists.
ST 5-HT antagonists
5-hydroxytryptamine antagonists
NT BF4.2e LSD    qh   ah
+BF10 bufotenine    qh   ah
 ZN2.10.6e phenoxybenzamine    qh   ah
 ZO2.2.2.12.2 fenclonine    qh   ah
 ZT4.28.6.2e risperidone    qh   ah
 ZT4.28.6.4e ritanserin    qh   ah
 ZT6.10.12.2e N,N-Dimethyltryptamine    qh   ah
 ZT6.20.2e ketanserin    qh   ah
 ZT8.4.2.2e clozapine    qh   ah
RT EE16.6e antagonistic drug interaction    qh   ah
 ZT6.10.12.4e serotonin    qh   ah
YV6.6.2e.  .  .  .  serotonin uptake inhibitors   qh
SN A group of drugs that inhibit neuronal re-uptake of serotonin, and consequently prolong its action. Such drugs have been reported to cause a reduction in alcohol consumption. Certain antidepressants share the property of inhibiting serotonin uptake, while also inhibiting noradrenaline (norepinephrine) uptake.
ST 5 HT sub 2
5 HT sub 3
5-hydroxytryptamine uptake inhibitors
serotonin receptor inhibitors
serotonin reuptake inhibitors
NT ZF8.6.2.2.2e sertraline    qh   ah
 ZN2.4.2e fluoxetine    qh   ah
 ZN2.4.4e citalopram    qh   ah
 ZN2.12e fluvoxamine    qh   ah
 ZT4.14.10 ondansetron    qh   ah
 ZT4.18.4e trazodone    qh   ah
 ZT4.20.2e paroxetine    qh   ah
+ZT4.26.4.2.2e zimelidine    qh   ah
 ZT8.6.2.2e amoxapine    qh   ah
BT+YP4.8.2.2e serotonergic anti-alcohol-craving agents    qh   ah
+YP4.8.12.6 agents for alcohol-concurrent depression    qh   ah
+YP4.8.12.10 agents for alcohol-related cognitive impairment    qh   ah
YV6.6.2.2.  .  .  .  .  viqualine   qh
BT+YP4.8.2.2e serotonergic anti-alcohol-craving agents    qh   ah
YV6.6.2.4.  .  .  .  .  amterozide   qh
BT+YP4.8.2.10 neuropeptide anti-alcohol-craving agents    qh   ah
YV8e.  .  parasympatholytics   qh
HN ETOH descriptor 2000.
ST anticholinergic agents
anticholinergics
NT+YD10.2 cholinesterase reactivators    qh   ah
 ZJ2.10.4.4.2e quinuclidinyl benzilate    qh   ah
+ZP18e solanaceous alkaloids    qh   ah
 ZP18.6.4e nicotinamide    qh   ah
+ZQ12.2e papaverine    qh   ah
BT+YW8e CNS stimulants    qh   ah
YV8.2.  .  .  ganglionic blockaders   qh
ST ganglionic blockers
NT BD2e nicotine    qh   ah
 ZU6.2e mecamylamine    qh   ah
YV10e.  .  parasympathomimetics   qh
HN ETOH descriptor 2000.
SN A substance that produces actions similar to the stimulation of the parasympathetic nervous system. Also called cholinomimetic.
ST cholinomimetic
NT+YD8.4 cholinesterase inhibitors    qh   ah
 ZP12e physostigmine    qh   ah
YV10.2e.  .  .  carbachol   qh
HN Introduced 1995.
YV10.4.  .  .  ganglionic stimulants   qh
NT BD2e nicotine    qh   ah
 ZP14e pilocarpine    qh   ah
 ZT4.32.2.2e tremorine    qh   ah
 ZT4.32.6.2e oxotremorine    qh   ah
YV12e.  .  sympatholytics   qh
HN ETOH descriptor 2000.
RT+YK6.2e adrenergic receptors    qh   ah
YV12.2e.  .  .  alpha-adrenergic receptor blockaders   qh
ST alpha-2 adrenergic antagonists
NT ZN2.10.6e phenoxybenzamine    qh   ah
 ZP26.4e yohimbine    qh   ah
 ZT4.14.12e phentolamine    qh   ah
 ZT4.14.14e tolazoline    qh   ah
 ZT6.20.6e prazosin    qh   ah
RT+YK6.2e adrenergic receptors    qh   ah
YV12.4e.  .  .  beta-adrenergic receptor blockaders   qh
NT ZN2.16.2.6e sotalol    qh   ah
 ZN2.16.2.12.4.2e propranolol    qh   ah
RT+YK6.2e adrenergic receptors    qh   ah
YV12.6.  .  .  adrenergic neurohumor depleters   qh
NT+ZP26e rauwolfia alkaloids    qh   ah
RT+YK6.2e adrenergic receptors    qh   ah
YV14e.  .  sympathomimetics   qh
HN ETOH descriptor 2000.
SN A drug that primarily mimics or produces effects similar to those resulting from stimulation of the sympathetic nervous system. Sympathomimetic drugs that also excite the central nervous system (CNS), such as the amphetamines, are used as recreational drugs. Also called adrenomimetic drugs.
ST adrenomimetic drugs
NT+ZN2.10.2e fenfluramine    qh   ah
+ZN2.18.2.2.4e tyramine    qh   ah
RT+YK6.2e adrenergic receptors    qh   ah
YV14.2e.  .  .  adrenergic receptor agonists   qh
RT EE16.4e synergistic drug interaction    qh   ah
YV14.2.2e.  .  .  .  alpha-adrenergic receptor agonists   qh
ST alpha adrenergic agonists
NT+YH2.2.6e epinephrine    qh   ah
+YH2.2.6.6e norepinephrine    qh   ah
 ZN2.16.2.4e phenylephrine    qh   ah
RT+YP4.6e alcohol withdrawal agents    qh   ah
YV14.2.2.2.  .  .  .  .  adrenergic alpha-2 adrenergic agonists   qh
YV14.2.4e.  .  .  .  beta-adrenergic receptor agonists   qh
NT+YH2.2.6.6e norepinephrine    qh   ah
 ZN2.16.2.14e ritodrine    qh   ah
+ZQ12.2.2e papaveroline    qh   ah
YV14.4e.  .  .  neurotransmitter uptake inhibitors   qh
HN ETOH descriptor 2000.
ST neuronal transmitter uptake inhibitors
RT EE16.6e antagonistic drug interaction    qh   ah
+EW6e neurotransmission    qh   ah
+YJ2e neurotransmitters    qh   ah


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