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Drilldown: Medicines
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Choose a table:
Medicines (732)
Medicines
> halflife
:
1-2 hours (parent compound)'"`UNIQ--ref-00000029-QINU`"'
or
None
Use the filters below to narrow your results.
generic:
brand:
None
(236)
Other values:
''Areca catechu'' (the nut); ''Piper betle'' (the leaf)
''Brugmansia'' spp., Angel's trumpet, ''borrachero'', ''toé''
''Catha edulis''. Chat, qat, the Flower of Paradise
''Cola nitida'', ''Cola acuminata''
''Erythroxylum coca'', ''E. novogranatense''
''Ilex paraguariensis''
''Ilex vomitoria''
''Mimosa tenuiflora''. Jurema preta, tepescohuite
''Myristica fragrans''. Mace (the fruit aril)
''Paullinia cupana''
''Sophora secundiflora''. Texas mountain laurel, frijolillo
''Theobroma cacao''
Akineton
Alfenta
Amerge
Amidate
Amytal
Anafranil
Antabuse
Apokyn
Aptiom
Artane
Aurorix
Axert
Azilect
Banzel
Benzedrex
Betapace
Brevibloc
Brevital
Briviact
Cafergot
Campral
Captagon
Cerebyx
Cesamet
Chantix
Clozaril
Cogentin
Compazine
Comtan
Corgard
Dalmane
Darvon
Deadly nightshade
Demerol
Depakote
Desoxyn
Dexedrine
DHE
Diacomit
Dilantin
Dilaudid
Diprivan
Dolophine
Doral
Doriden
Dostinex
Dramamine
Duragesic
DXM
DXO
Edronax
Eldepryl
Epidiolex
Exelon
Fanapt
Felbatol
Feldene
Fetzima
Fintepla
Frova
Fycompa
Gabitril
Geodon
Halcion
Henbane, black henbane
Heroin
Hetlioz
Imovane
Inapsine
Invega
ketalar
Krokodil
Latuda
Laudanum, Dropizol
Lexotan
Librium
Lithobid
Loxitane
Lucemyra
Ludiomil
Luminal
Lunesta
Mandrake
Marinol
Marplan
Mellaril
Miltown
Moban
Mogadon
Narcan
Nardil
Navane
Nembutal
Neupro
Norflex
Norpramin
Nubain
Nucynta
Nuvigil
O-DSMT
Onfi
Ongentys
Opana
Orap
Parafon Forte
Parlodel
Parnate
Pentothal
Placidyl
Precedex
Prolixin
ProSom
Provigil
Quaalude
Qulipta
Razadyne
Reed canary grass
Relpax
Restoril
Reyvow
Rohypnol
Rozerem
Sabril
Saphris
Sativex
Savella
Seconal
Selincro
Serax
Serzone
Sinemet
Skelaxin
Soma
Sonata
Sonoran Desert Toad, Colorado River Toad
Stablon
Stadol
Stelazine
Suboxone
Sufenta
Surmontil
Symmetrel
Talwin
Tantum
Tasmar
The ayahuasca vine, ''yagé'', ''caapi'', ''mariri''
THIP
Thorazine
Tofranil
Transderm
Tranxene
Trilafon
Tylenol, Panadol
Ubrelvy
Ultiva
Unisom
Valdoxan
Versed
Vicodin
Vimpat
Vivactil
Vivitrol
Voltaren (IR oral, topical gel), Cataflam (potassium IR), Cambia (oral powder, migraine), Zorvolex (low-dose), Pennsaid (topical 2% solution), Flector (transdermal patch), Solaraze (3% gel for actinic keratosis)
Wormwood, absinthe, la Fée Verte, the Green Muse
Xadago
Xcopri
Xyrem
Zarontin
Zomig
Zonegran
Search
classes:
Research material (131)
·
Classic Psychedelic (69)
·
Stimulant (43)
·
Opioid (31)
·
Sedative-Hypnotic (29)
·
Tryptamine (26)
·
Phenethylamine (25)
·
Botanical (23)
·
Benzodiazepine (22)
·
Anticonvulsant (19)
·
Dissociative (19)
·
Analgesic (17)
·
Antidepressant (17)
·
Antipsychotic (17)
·
Plant Medicine (17)
·
Antiparkinsonian (16)
·
Empathogen (16)
·
Neuroleptic (16)
·
Cathinone (14)
·
Nootropic (13)
Other values:
_none
AChE inhibitor
Addiction medicine
Alpha-2 agonist
Amphetamine
Amphetamine-like
Analgesic / antipyretic
Anesthetic
Anesthetic adjunct
Animal Medicine
Anti-dementia
Anticholinergic
Antiemetic
Antihistamine
Anxiolytic
Barbiturate
Benzofuran
Beta blocker
Caffeine plant
Cannabinoid
Cannabinoid (minor)
Cathinone source
COMT inhibitor
Daimonica
Decongestant
Deliriant
Dopamine agonist
Empathogenica
Ergotamine
Eugeroic
Excitantia
GABAergic
Gepant
GLP-1 receptor agonist
Inhalant
Inhalational anesthetic
Local anesthetic
Lysergamide
MAO-B inhibitor
MAOI
Migraine medicine
Mood Stabilizer
Muscle relaxant
Neuromuscular blocker
NRI
NSAID
Oneirogen
Opioid antagonist
Peptide
Phantastica
Pharmaceutical
Phenidate
phytocannabinoid
Piperazine
Plant Med
precursor cannabinoid
Psychedelic
Psychostimulant
Pyrrolidinophenone
Racetam
Rhapsodica
RIMA
SARI
Sedative
SNRI
Synthetic cannabinoid
TCA
THC oxidation product
Thienodiazepine
Trace amine
Triptan
Tropane alkaloid plant
Xanthine
Z-drug
[[:Category:Analgesics|Analgesic]]
[[:Category:NSAIDs|Non-steroidal anti-inflammatory (NSAID)]]
Search
mechanism:
5-HT2A agonist (27)
·
GABAA positive allosteric modulator (22)
·
None
(12)
·
Monoamine releasing agent (11)
·
CB1/CB2 agonist (7)
·
Potent mu-opioid receptor agonist (6)
·
Sodium channel blocker (6)
·
Dopamine/norepinephrine reuptake inhibitor (5)
·
GABAA potentiator; NMDA antagonist (5)
·
Phenothiazine D2 antagonist (5)
·
Potent 5-HT2A agonist (5)
·
5-HT1B/1D agonist (4)
·
LSD analogue; 5-HT2A agonist (4)
·
Mu-opioid receptor agonist (4)
·
Muscarinic receptor antagonist (4)
·
Prodrug of LSD; 5-HT2A agonist (4)
·
Selective norepinephrine reuptake inhibitor (4)
uses:
None
(395)
·
Antimanic, Antidepressive, Antisuicide (1)
·
Pain, cough, disquiet (1)
·
'"`UNIQ--vote-00000006-QINU`"' (5)
·
'"`UNIQ--vote-00000008-QINU`"', '"`UNIQ--vote-00000009-QINU`"' (8)
·
'"`UNIQ--vote-0000000C-QINU`"', '"`UNIQ--vote-0000000D-QINU`"', '"`UNIQ--vote-0000000E-QINU`"', '"`UNIQ--vote-0000000F-QINU`"' (1)
·
'"`UNIQ--vote-00000021-QINU`"', '"`UNIQ--vote-00000022-QINU`"', '"`UNIQ--vote-00000023-QINU`"', '"`UNIQ--vote-00000024-QINU`"', '"`UNIQ--vote-00000025-QINU`"', '"`UNIQ--vote-00000026-QINU`"', '"`UNIQ--vote-00000027-QINU`"', '"`UNIQ--vote-00000028-QINU`"' (1)
·
'"`UNIQ--vote-00000065-QINU`"' (1)
·
'"`UNIQ--vote-000000AD-QINU`"', '"`UNIQ--vote-000000AE-QINU`"' (1)
·
'"`UNIQ--vote-000003A0-QINU`"', '"`UNIQ--vote-000003A1-QINU`"' (1)
·
'"`UNIQ--vote-000004B9-QINU`"', '"`UNIQ--vote-000004BA-QINU`"', '"`UNIQ--vote-000004BB-QINU`"' (1)
·
'"`UNIQ--vote-0000069B-QINU`"', '"`UNIQ--vote-0000069C-QINU`"' (1)
·
'"`UNIQ--vote-0000081E-QINU`"' (1)
starting dose:
None
(413)
·
0.5–1 oz (10–30 g) ground for psychoactive effect; far smaller for culinary use (1)
·
5 mg PO (1)
·
A ''marduuf'' bundle (~50 g fresh leaves) chewed over a couple of hours (1)
·
A measured pour of absinthe diluted 5:1 with cold water over sugar (the louche ritual) (1)
·
IR oral 50 mg PO TID or 75 mg BID. Voltaren 1% gel: apply 2-4 g to affected area QID. Pennsaid 2%: 40 drops to knee BID. Flector patch: every 12 hours (1)
preparations:
None
(397)
·
A ''betel quid'': areca nut slice + betel leaf + slaked lime (calcium hydroxide) ± tobacco ± spices, chewed (1)
·
Acid/base extraction of fresh young grass for tryptamines; combined with an MAOI (1)
·
Bark/woody stem decocted with a DMT-source plant (''Psychotria viridis'', ''Diplopterys cabrerana'') to make ayahuasca (1)
·
Bright red seeds, traditionally ingested or smoked. Highly toxic, narrow margin between active and lethal (1)
·
Desoxyn 5 mg tabs (1)
·
Dried leaves and twigs, infused in a gourd (''mate'') and drunk through a metal straw (''bombilla'') (1)
·
Dried leaves; absinthe liqueur (120–160 proof, with hyssop, lemon balm, fennel, anise, sometimes Acorus calamus) (1)
·
Fermented and roasted seeds, ground. Mexican tradition: drunk with chili, cornmeal, achiote. European tradition: with sugar and milk (1)
·
Flowers or leaves infused or smoked. Highly variable potency; narrow toxic margin (1)
·
Fresh leaves and tender twigs chewed; degrades on drying (1)
·
Fresh nuts chewed; also dried and powdered (1)
·
Ground dried seed (nutmeg) or fruit aril (mace); occasionally infused (1)
·
IR tablets 25, 50 mg; ER tablets 100 mg; Cataflam IR 50 mg; Zorvolex 18, 35 mg; Voltaren gel 1%; Pennsaid 2% topical solution; Flector transdermal patch; Solaraze 3% gel; Cambia oral powder 50 mg (1)
·
Leaves and seeds, traditionally smoked or infused. Possibly the original Pythia oracle plant (1)
·
Leaves chewed with a pinch of slaked lime (the lime converts cocaine HCl to freebase for buccal absorption); also drunk as tea (''mate de coca'') (1)
·
Leaves, berries, root. Historically: belladonna cigarettes ("Asthmador") OTC in US until the 1970s (1)
·
Parotid-gland venom expressed onto a glass plate, dried into a shellac-like resin, vaporized and inhaled (1)
·
Roasted seeds ground to powder, mixed with water; commercial syrups and energy drinks (1)
·
Root bark acid/base-extracted for DMT; or as the resurrected ''jurema preta'' brew (decocted with an MAOI such as ''Peganum harmala'') (1)
·
Root, traditionally carved into ''mannikens'' or infused into wine (1)
·
Toasted leaves and twigs decocted to a near-black concentrate (1)
fda max:
None
(416)
·
150 mg/day (oral); use lowest effective dose for shortest duration per FDA NSAID class guidance (1)
·
25 mg/day (ADHD per Desoxyn label); 15 mg/day (obesity, short-term, per Desoxyn label) (1)
routes:
None
(397)
·
buccal); refined cocaine has its own profile (1)
·
inhalation (2)
·
Inhalation (vaporized) (1)
·
Oral (14)
·
Oral (buccal absorption) (1)
·
Oral (buccal) (1)
·
Oral (leaf (1)
·
Oral (prescribed) (1)
·
Oral (with MAOI) (2)
·
oral powder (Cambia for migraine) (1)
·
smoked (extracted DMT) (1)
·
topical (2)
·
transdermal (1)
onset:
None
(414)
·
15–30 min (1)
·
30-60 minutes (oral); slower for topical (1)
·
Seconds (1)
·
Slow, 2–6 h (1)
duration:
None
(414)
·
12–24 h or longer (1)
·
2–4 h (1)
·
6-8 hours (IR oral); 12-24 hours (ER) (1)
·
~15 min (1)
halflife:
(Click arrow to add another value)
None
·
~12 hours
·
~27 days
·
~5 h (caffeine)
·
'''Autoinduction''': 25-65 hours initially, falling to 12-17 hours after 2-3 weeks of dosing as carbamazepine induces its own CYP3A4 metabolism. Major clinical implication: doses require re-titration after the autoinduction period'"`UNIQ--ref-0000001D-QINU`"'
·
0.5-1.5 hours (plasma); pharmacodynamic effect persists 24+ hours'"`UNIQ--ref-000000DE-QINU`"'
·
1-1.3 hours'"`UNIQ--ref-000001A1-QINU`"'
·
1-1.5 hours'"`UNIQ--ref-00000DE3-QINU`"'
·
1-2 hours (parent compound)'"`UNIQ--ref-00000029-QINU`"'
·
1-2 hours (parent); 18-30 hours for active metabolite oxypurinol'"`UNIQ--ref-0000030F-QINU`"'
·
1-2 hours'"`UNIQ--ref-00000017-QINU`"'
·
1-3 hours (normal liver); markedly prolonged in overdose with glutathione depletion'"`UNIQ--ref-000006A5-QINU`"'
·
1-3 minutes (very short)'"`UNIQ--ref-00000C0F-QINU`"'
·
1.4 hours (parent); 13-24 hours for active metabolite canrenone'"`UNIQ--ref-00000354-QINU`"'
·
1.5-2 hours (longer in renal failure)'"`UNIQ--ref-00000222-QINU`"'
·
1.5-2 hours'"`UNIQ--ref-00000020-QINU`"'
·
10-11 hours (benazeprilat, the active metabolite)'"`UNIQ--ref-00000A22-QINU`"'
·
11-13 h (immediate-release); 11-16 h (extended-release)
·
11-15 hours'"`UNIQ--ref-00000842-QINU`"'
·
12-15 hours (intermediate); '''no active metabolites''' (key clinical feature)'"`UNIQ--ref-00000023-QINU`"'
Other values:
12-15 hours'"`UNIQ--ref-00000022-QINU`"'
12-16 hours'"`UNIQ--ref-00000026-QINU`"'
12-17 hours'"`UNIQ--ref-00000029-QINU`"'
14 hours (parent); 20-30 hours including active ortho- and para-hydroxylated metabolites'"`UNIQ--ref-0000001B-QINU`"'
14-25 hours (longer in elderly and hepatic impairment)'"`UNIQ--ref-00000026-QINU`"'
14–26 h (oral); ~3 weeks (decanoate)
15-20 hours'"`UNIQ--ref-00000020-QINU`"'
16-22 hours'"`UNIQ--ref-0000047D-QINU`"'
18 hours (IR); 32-33 hours (ER)'"`UNIQ--ref-0000001A-QINU`"'
18-44 hours'"`UNIQ--ref-00000020-QINU`"'
1–4 days (7–15 days for norfluoxetine)
2 hours (parent); 6-9 hours for active carboxylic acid metabolite EXP3174'"`UNIQ--ref-000000BC-QINU`"'
2 hours'"`UNIQ--ref-00000015-QINU`"'
2-3 hours (normal renal function); markedly prolonged in renal impairment'"`UNIQ--ref-000010B3-QINU`"'
2-3 hours (parent and active N-desethyl metabolite)'"`UNIQ--ref-000006E1-QINU`"'
2-3 hours'"`UNIQ--ref-00000012-QINU`"'
2-4 hours'"`UNIQ--ref-00000026-QINU`"'
2-5 hours (IR); ER formulations extend functional duration via osmotic/matrix release'"`UNIQ--ref-0000074D-QINU`"'
2-5 hours'"`UNIQ--ref-000002D9-QINU`"'
2.2 h (IR parent); ~3 h (XR parent)
2.5 hours (short, requires TID-QID dosing)'"`UNIQ--ref-0000001D-QINU`"'
2.5-3.5 hours; longer in renal impairment'"`UNIQ--ref-0000025B-QINU`"'
2.5–3 hours
2.7-5.5 hours'"`UNIQ--ref-0000015E-QINU`"'
20-40 hours'"`UNIQ--ref-00000023-QINU`"'
21-54 hours'"`UNIQ--ref-00000026-QINU`"'
24–42 h (buprenorphine); 1–2 h (naloxone)
27-32 hours'"`UNIQ--ref-00000026-QINU`"'
2–3 h
2–3 h (parent compound)
3-10 hours (low dose); 8-15 hours (high dose); much longer in third-space accumulation (pleural effusion, ascites)'"`UNIQ--ref-000007C8-QINU`"'
3-4 hours (similar between PO and IV due to high oral bioavailability)'"`UNIQ--ref-00000B46-QINU`"'
3-4 hours'"`UNIQ--ref-00000026-QINU`"'
3-4.5 hours (IR); 5-7 hours (ER; effective duration 24 hours via formulation)'"`UNIQ--ref-00000642-QINU`"'
3-5 hours (IR); 4.5 hours (ER)'"`UNIQ--ref-0000001D-QINU`"'
3-6 hours (longer in hepatic impairment)'"`UNIQ--ref-00000378-QINU`"'
3-7 hours (IR); functional 24 hours (ER)'"`UNIQ--ref-00000A6B-QINU`"'
3-7 hours (slow acetylators) vs 1-3 hours (rapid acetylators) via NAT2 polymorphism'"`UNIQ--ref-00000687-QINU`"'
30-40 hours (long; accumulates with chronic dosing)'"`UNIQ--ref-00000026-QINU`"'
30-50 hours'"`UNIQ--ref-00000078-QINU`"'
30-50 minutes (short)'"`UNIQ--ref-00000021-QINU`"'
30–60 min
36-42 hours (R/S enantiomers differ; S-warfarin is 2-5× more potent and cleared by CYP2C9)'"`UNIQ--ref-00000705-QINU`"'
3–5 hours
3–6 h
3–7 h
4 hours'"`UNIQ--ref-00000938-QINU`"'
4-5 hours'"`UNIQ--ref-00000026-QINU`"'
4-6 hours (inhaled and PO)'"`UNIQ--ref-00000099-QINU`"'
4-8 hours (longer in elderly, 9-13 hours)'"`UNIQ--ref-00000026-QINU`"'
40-60 hours (notable for the thiazide class)'"`UNIQ--ref-00000783-QINU`"'
4–5 h
5-6 hours'"`UNIQ--ref-00000020-QINU`"'
5-6 hours'"`UNIQ--ref-00000EF9-QINU`"'
5-7 hours'"`UNIQ--ref-00000029-QINU`"'
5-9 hours (elderly: 11-13 hours)'"`UNIQ--ref-00000513-QINU`"'
6-15 hours'"`UNIQ--ref-0000013E-QINU`"'
6-8 hours'"`UNIQ--ref-0000001F-QINU`"'
6-8 hours'"`UNIQ--ref-00000BEB-QINU`"'
6-9 hours (substantially longer in renal impairment due to renal elimination)'"`UNIQ--ref-00000020-QINU`"'
6.2 hours (plasma); ~17 hours in erythrocytes'"`UNIQ--ref-00000018-QINU`"'
6.3 hours'"`UNIQ--ref-00000026-QINU`"'
60-100 hours (long)'"`UNIQ--ref-0000001B-QINU`"'
7-10 hours'"`UNIQ--ref-0000001B-QINU`"'
8-10 hours (longer in elderly and renal impairment)'"`UNIQ--ref-00000396-QINU`"'
8-12 hours (longer in elderly and renal impairment)'"`UNIQ--ref-0000001B-QINU`"'
8-16 hours'"`UNIQ--ref-0000001E-QINU`"'
9-15 hours'"`UNIQ--ref-000001BC-QINU`"'
9-16 hours (pH-dependent: acidic urine shortens, alkaline urine substantially extends)'"`UNIQ--ref-0000001B-QINU`"'
9-16 hours'"`UNIQ--ref-0000097C-QINU`"'
9–12 h
9–12 minutes (intravenous)
Amitriptyline 10-50 hours (highly variable); nortriptyline active metabolite 18-44 hours'"`UNIQ--ref-00000026-QINU`"'
Aqueous crystalline ~30 minutes; benzathine effective ~3 weeks via depot release'"`UNIQ--ref-00001419-QINU`"'
Aspirin 15-30 minutes; salicylate metabolite 2-3 hours (concentration-dependent, saturable at high doses)'"`UNIQ--ref-00000027-QINU`"'
Biphasic: ~3-6 hours alpha, ~5-9 hours beta'"`UNIQ--ref-0000001D-QINU`"'
Bupropion ~21 hours; hydroxybupropion (active metabolite) ~20-37 hours'"`UNIQ--ref-00000023-QINU`"'
Buspirone 2-3 hours; 1-PP active metabolite 4-6 hours'"`UNIQ--ref-0000001D-QINU`"'
Butalbital ~35 hours (long; cumulative effects with frequent use); acetaminophen 1-3 hours; caffeine 3-7 hours'"`UNIQ--ref-0000159F-QINU`"'
Butalbital ~35 hours; aspirin (acetyl group) ~15 minutes, salicylate 2-3 hours; caffeine 3-7 hours'"`UNIQ--ref-000015B7-QINU`"'
Cariprazine ~2-4 d; major active metabolites desmethyl-cariprazine (DCAR) ~1-3 weeks → 'oral depot' effect with delayed steady-state and reduced effect of missed doses
Codeine 2.5-3.5 hours; acetaminophen 1-3 hours'"`UNIQ--ref-00001517-QINU`"'
D-amphetamine ~10 h; L-amphetamine ~13 h (adults)
Dextromethorphan substantially prolonged by quinidine's CYP2D6 inhibition (typical extensive metabolizers see ~10× higher AUC); quinidine ~6-8 hours'"`UNIQ--ref-00001583-QINU`"'
Dextromethorphan ~22 h (when CYP2D6 inhibited); bupropion ~21 h
Diazepam 20-50 hours; '''N-desmethyldiazepam (nordazepam) 30-200 hours''' is the major active metabolite and accumulates substantially with chronic dosing'"`UNIQ--ref-00000026-QINU`"'
Estimated ~12–17 h (some sources cite up to ~21 h); active metabolites prolong effect.
Highly variable by formulation; native T is hours
Highly variable, 7-46 hours (mean ~21 h); lipophilic deposition in fat with delayed re-release contributes to wide range'"`UNIQ--ref-00000065-QINU`"'
Mononitrate ~5 hours; dinitrate ~1 hour'"`UNIQ--ref-00001461-QINU`"'
Morphine 2-4 hours; morphine-6-glucuronide active metabolite 2-4 hours (longer with renal impairment)'"`UNIQ--ref-00000020-QINU`"'
N/A (incorporated into hemoglobin and tissue stores)
Naltrexone ~4 hours (6β-naltrexol metabolite ~13 hours); bupropion ~21 hours'"`UNIQ--ref-00001568-QINU`"'
Not absorbed
Not applicable (electrolyte and buffer)
Not applicable (electrolyte solution)
Not applicable (electrolyte)
Not formally established
Not meaningfully described
Not meaningfully described (electrolyte)
Not meaningfully described (electrolyte; renally cleared)
Not meaningfully described (minimal systemic absorption from topical use)'"`UNIQ--ref-00000F45-QINU`"'
Not meaningfully described (negligible systemic absorption from intact skin or oral mucosa)'"`UNIQ--ref-00001398-QINU`"'
Not meaningfully described (negligible systemic absorption — the drug acts locally and is degraded in the GI tract)'"`UNIQ--ref-0000119C-QINU`"'
Not meaningfully described (negligible systemic absorption)
Not meaningfully described (not systemically absorbed)'"`UNIQ--ref-00000D17-QINU`"'
Not meaningfully described (topical local action)'"`UNIQ--ref-00001239-QINU`"'
Not meaningfully described for an electrolyte; distribution between intra- and extracellular compartments is the relevant kinetic
Not meaningfully described for ophthalmic use'"`UNIQ--ref-00001287-QINU`"'
Not meaningfully described for topical use (systemic exposure varies with surface area, occlusion, skin integrity)'"`UNIQ--ref-0000079E-QINU`"'
Not meaningfully described for topical use'"`UNIQ--ref-00000A02-QINU`"'
Not meaningfully described — lactulose is not significantly absorbed
Not meaningfully described — sucralfate is essentially non-absorbed'"`UNIQ--ref-00000DC2-QINU`"'
Not meaningfully described — topical local action with minimal systemic absorption'"`UNIQ--ref-00001218-QINU`"'
Not well characterized
Not well characterized; tissue incorporation over weeks'"`UNIQ--ref-00000051-QINU`"'
Not well characterized'"`UNIQ--ref-00000018-QINU`"'
Olanzapine ~30 hours; fluoxetine 1-4 days (norfluoxetine 7-15 days)'"`UNIQ--ref-0000154D-QINU`"'
Oxcarbazepine 2 hours; '''10-monohydroxy active metabolite (MHD) ~9 hours''' (the agent that produces essentially all of the clinical effect)'"`UNIQ--ref-0000001A-QINU`"'
Oxycodone 3-5 hours; acetaminophen 1-3 hours'"`UNIQ--ref-000014E2-QINU`"'
Oxycodone 3-5 hours; aspirin (acetyl group) 15-20 minutes, salicylate 2-3 hours at therapeutic doses'"`UNIQ--ref-000014FA-QINU`"'
Parent lisdexamfetamine <1 hour; dextroamphetamine 10-12 hours after release'"`UNIQ--ref-00000017-QINU`"'
Plasma 2-3 hours; biologic ~18-36 hours'"`UNIQ--ref-00000867-QINU`"'
Plasma 2-3 hours; biologic ~18-36 hours'"`UNIQ--ref-000008C4-QINU`"'
Plasma 3-4 hours; biologic ~12-36 hours'"`UNIQ--ref-000002A3-QINU`"'
Plasma ~1-2 hours; biologic ~8-12 hours'"`UNIQ--ref-00000AD1-QINU`"'
Plasma ~3 hours; bone half-life ~10 years'"`UNIQ--ref-000006C3-QINU`"'
Plasma ~3-4.5 hours; biologic ~36-72 hours'"`UNIQ--ref-00000E2B-QINU`"'
Plasma ~3-5 hours; biologic effect substantially longer (~12-36 hours for intermediate-acting glucocorticoids)'"`UNIQ--ref-00000666-QINU`"'
Plasma ~5 hours; biologic ~36-54 hours'"`UNIQ--ref-0000101A-QINU`"'
Primidone 5-15 hours; '''phenobarbital active metabolite 50-150 hours'''; PEMA (phenylethylmalonamide) active metabolite 16 hours'"`UNIQ--ref-00000017-QINU`"'
Psilocin: ~2-3 h; psilocybin itself is a prodrug, dephosphorylated within minutes of absorption
Risperidone 3-20 hours; '''9-hydroxy-risperidone (paliperidone) ~20-24 hours''' is the major active metabolite and is separately marketed as a parent compound (Invega)'"`UNIQ--ref-00000021-QINU`"'
Sumatriptan ~2.5 hours; naproxen 12-15 hours'"`UNIQ--ref-000015D1-QINU`"'
T4 ~7 days; T3 ~1 day'"`UNIQ--ref-00000036-QINU`"'
Tissue half-life not formally measured; clinical effect ~12 weeks
Topical: not meaningfully described; oral 2-8 hours'"`UNIQ--ref-00000888-QINU`"'
Tramadol 6-7 hours; M1 active metabolite 7-9 hours'"`UNIQ--ref-0000001D-QINU`"'
Tramadol ~5-7 hours (M1 metabolite ~9 hours); acetaminophen 1-3 hours'"`UNIQ--ref-00001530-QINU`"'
Variable; effect dependent on local intestinal action rather than systemic kinetics'"`UNIQ--ref-0000106B-QINU`"'
Venlafaxine 5 hours; desvenlafaxine active metabolite 11 hours'"`UNIQ--ref-00000026-QINU`"'
~0.5 hours plasma; tissue retention longer
~0.5-2 hours (oral)'"`UNIQ--ref-00000BA3-QINU`"'
~1 day (much shorter than T4's ~7 days)'"`UNIQ--ref-0000149D-QINU`"'
~1 hour (IR niacin); ER formulations extend functional duration'"`UNIQ--ref-00001038-QINU`"'
~1 hour (plasma); pharmacodynamic effect persists 24+ hours'"`UNIQ--ref-0000011D-QINU`"'
~1 hour SC'"`UNIQ--ref-00000589-QINU`"'
~1 hour'"`UNIQ--ref-000004F2-QINU`"'
~1 hour'"`UNIQ--ref-00001050-QINU`"'
~1-2 hours plasma (riboflavin itself); FAD/FMN tissue cofactors are continuous
~1.5 hours (plasma); pharmacodynamic effect 24+ hours via target turnover'"`UNIQ--ref-000008E8-QINU`"'
~1.5 hours'"`UNIQ--ref-00000FF9-QINU`"'
~1.5-2 hours'"`UNIQ--ref-00000D3E-QINU`"'
~1.7 hours'"`UNIQ--ref-000009E4-QINU`"'
~1.8 hours (initial); ~10 hours (terminal)'"`UNIQ--ref-00000B25-QINU`"'
~10 h (CYP2D6 extensive metabolizers); up to 31 h (poor metabolizers)
~10-20 days (steady-state body pool); single dose plasma ~2 hours
~10-20 minutes systemically (rapid hepatic and erythrocyte dihydropyrimidine dehydrogenase clearance)'"`UNIQ--ref-000011BE-QINU`"'
~11 h
~11 hours (enalaprilat, the active metabolite)'"`UNIQ--ref-00000B84-QINU`"'
~11 hours'"`UNIQ--ref-00000015-QINU`"'
~11 hours'"`UNIQ--ref-0000001A-QINU`"'
~11 hours'"`UNIQ--ref-00000029-QINU`"'
~11-17 days'"`UNIQ--ref-0000147F-QINU`"'
~12 hours (effective); terminal half-life is biphasic'"`UNIQ--ref-00000059-QINU`"'
~12 hours (effective); terminal much longer'"`UNIQ--ref-0000117C-QINU`"'
~12 hours apparent (functional duration ~24 hours due to depot release kinetics)'"`UNIQ--ref-0000023B-QINU`"'
~12 hours'"`UNIQ--ref-000001FB-QINU`"'
~12 hours'"`UNIQ--ref-00000D82-QINU`"'
~12 hours'"`UNIQ--ref-0000111F-QINU`"'
~12.1 days
~12.4 hours'"`UNIQ--ref-0000027C-QINU`"'
~12.4 hours'"`UNIQ--ref-00000765-QINU`"'
~12.9 hours'"`UNIQ--ref-00000552-QINU`"'
~13 hours'"`UNIQ--ref-0000018A-QINU`"'
~13 hours'"`UNIQ--ref-0000056C-QINU`"'
~13-17 hours (ramiprilat, the active metabolite)'"`UNIQ--ref-00000C32-QINU`"'
~13-20 hours (oral); transdermal pharmacokinetics buffer the peaks/troughs of oral dosing'"`UNIQ--ref-000003BA-QINU`"'
~14 days'"`UNIQ--ref-00001103-QINU`"'
~14 hours (adults); longer in elderly and renal impairment'"`UNIQ--ref-0000113F-QINU`"'
~14 hours'"`UNIQ--ref-00000CCC-QINU`"'
~15 hours (IR)'"`UNIQ--ref-00000023-QINU`"'
~15 hours (parent); nordoxepin active metabolite ~30 hours'"`UNIQ--ref-00000020-QINU`"'
~16-18 hours'"`UNIQ--ref-00001092-QINU`"'
~16-23 hours
~165 hours (~1 week), among the longest of any GLP-1 RA'"`UNIQ--ref-00000253-QINU`"'
~17 minutes (free acid, the active form, in aqueous humor)'"`UNIQ--ref-00000417-QINU`"'
~17-18 hours (Intuniv ER); ~17 hours (immediate-release)'"`UNIQ--ref-00000020-QINU`"'
~17-19 hours (longer than daridorexant)
~17.5 h
~18 hours (terminal)
~19 hours'"`UNIQ--ref-000000FC-QINU`"'
~2 hours (parent and active β-hydroxy acid metabolite); pharmacodynamic effect lasts 24 hours via target turnover'"`UNIQ--ref-0000017A-QINU`"'
~2 hours (plasma; minimal relevance — local-action drug)'"`UNIQ--ref-00000F7B-QINU`"'
~2 minutes'"`UNIQ--ref-00000E52-QINU`"'
~2-3 hours (parent); pharmacodynamic effect 24 hours via target turnover'"`UNIQ--ref-000003D5-QINU`"'
~2-3.6 hours (plasma)'"`UNIQ--ref-000009A5-QINU`"'
~2-4 hours (parent and active β-hydroxy acid metabolite); pharmacodynamic effect 24 hours via target turnover'"`UNIQ--ref-00000807-QINU`"'
~2.4 hours (Byetta, short, hence the BID schedule)'"`UNIQ--ref-000000ED-QINU`"' · Effective release half-life ~2 weeks (Bydureon)'"`UNIQ--ref-000000EE-QINU`"'
~2.5 hours'"`UNIQ--ref-0000001A-QINU`"'
~2.5-3 hours'"`UNIQ--ref-00001442-QINU`"'
~20 hours
~20 hours (fenofibric acid, the active metabolite)'"`UNIQ--ref-000004AD-QINU`"'
~20-60 minutes (plasma; not the relevant kinetic since urinary concentration matters)'"`UNIQ--ref-000008A3-QINU`"'
~21 hours (with nonlinear pharmacokinetics from CYP2D6 autoinhibition)'"`UNIQ--ref-0000002B-QINU`"'
~21 hours'"`UNIQ--ref-00000028-QINU`"'
~22 hours (parent + active glucuronide)'"`UNIQ--ref-00000450-QINU`"'
~22 hours; longer 54 hours (desmethylazelastine, active metabolite)'"`UNIQ--ref-000013B6-QINU`"'
~22 hours'"`UNIQ--ref-00000AB0-QINU`"'
~24 hours (6-methoxy-2-naphthylacetic acid, the active metabolite)'"`UNIQ--ref-000011F9-QINU`"'
~24 hours (longest of the ARB class; suits patients with morning BP surge)'"`UNIQ--ref-00000AEE-QINU`"'
~24 hours (parent); ~15 days (25(OH)D); 25(OH)D stores persist for months'"`UNIQ--ref-00000330-QINU`"'
~24 hours (parent); ~15 days (25(OH)D); tissue stores months
~25 days
~25 hours
~25 hours apparent (functional duration well over 42 hours from multi-hexamer depot)'"`UNIQ--ref-0000135A-QINU`"'
~25 hours'"`UNIQ--ref-0000129F-QINU`"'
~25-33 hours alone; ~15 hours with enzyme inducers; '''≥60 hours with valproate''' (UGT inhibition)'"`UNIQ--ref-00000025-QINU`"'
~25-44 hours plasma; receptor kinetics drive the once-daily duration'"`UNIQ--ref-000009C0-QINU`"'
~26 h (sertraline; range 13-45 h, longer in females); ~62-104 h (N-desmethylsertraline, weakly active)
~27-31 hours; markedly prolonged in renal/hepatic impairment and with CYP3A4 or P-gp inhibitors'"`UNIQ--ref-00000C72-QINU`"'
~28 days
~3 hours (acyclovir, the active metabolite); longer in renal impairment'"`UNIQ--ref-000005D6-QINU`"'
~3 hours (systemic, when measurable; topical action dominates)'"`UNIQ--ref-000011D9-QINU`"'
~3 hours; significantly prolonged in renal impairment'"`UNIQ--ref-0000090F-QINU`"'
~3 hours'"`UNIQ--ref-000010D1-QINU`"'
~3-4 days plasma; adipose tissue stores last months
~3-7 hours (parent); 16-24 hours including active metabolites'"`UNIQ--ref-00000824-QINU`"'
~30 hours (long, supports once-daily dosing and substantial drug-interaction window after discontinuation)'"`UNIQ--ref-00000A47-QINU`"'
~30-60 minutes'"`UNIQ--ref-00000E76-QINU`"'
~31 days
~35 hours'"`UNIQ--ref-00000026-QINU`"'
~36 hours (terminal much longer due to tissue accumulation in skin/nails)'"`UNIQ--ref-00000EB2-QINU`"'
~4 h
~4 hours (oral)'"`UNIQ--ref-0000001B-QINU`"'
~4 months in erythrocytes (carbonic anhydrase binding in red cells; not relevant to topical IOP duration)'"`UNIQ--ref-00000B0A-QINU`"'
~4-6 hours (plasma); intrathyroidal accumulation gives a much longer functional duration'"`UNIQ--ref-00000ED3-QINU`"'
~40 days (terminal; reflects extensive tissue distribution)'"`UNIQ--ref-000007EC-QINU`"'
~45 minutes (free acid in aqueous humor)'"`UNIQ--ref-00000DA1-QINU`"'
~45-68 hours'"`UNIQ--ref-00000DFE-QINU`"'
~5 days (~120 h)'"`UNIQ--ref-00000059-QINU`"'
~5 days (~120 h)'"`UNIQ--ref-00000303-QINU`"'
~5 h
~5 hours (plasma)'"`UNIQ--ref-00000F9C-QINU`"'
~5 hours in extensive CYP2D6 metabolizers; ~21 hours in CYP2D6 poor metabolizers'"`UNIQ--ref-00000014-QINU`"'
~5 weeks (much longer than finasteride's ~6 hours)'"`UNIQ--ref-00000D59-QINU`"'
~5-10 hours (5-ASA)'"`UNIQ--ref-00000BBE-QINU`"'
~5-20 hours (oral micronized; highly variable)'"`UNIQ--ref-00000726-QINU`"'
~5-6 hours in young men, ~8 hours in elderly'"`UNIQ--ref-00000531-QINU`"'
~5-7 days
~5-8 hours'"`UNIQ--ref-00001164-QINU`"'
~5-9 hours (parent and active metabolites combined)'"`UNIQ--ref-00000492-QINU`"'
~50 days (Depo-Provera; long depot release)'"`UNIQ--ref-00000F20-QINU`"'
~50 hours'"`UNIQ--ref-00000B64-QINU`"'
~50 hours'"`UNIQ--ref-00000C4E-QINU`"'
~57 hours (parent), ~200 h (active metabolite)
~58 days (parent); ~61 days (desethylamiodarone, active metabolite)'"`UNIQ--ref-00000CB3-QINU`"'
~6 days (plasma); hepatic stores last 3-5 years
~6 h (parent compound, immediate-release); ~9-12 h (active metabolite N-desalkylquetiapine, also called norquetiapine)
~6 hours (parent); active metabolite very short-lived but produces irreversible platelet effect'"`UNIQ--ref-000002C4-QINU`"'
~6 hours plasma; long bone retention
~6 hours'"`UNIQ--ref-00000015-QINU`"'
~6 hours'"`UNIQ--ref-00000018-QINU`"'
~6 hours'"`UNIQ--ref-000004CD-QINU`"'
~6-10 hours (oseltamivir carboxylate, the active metabolite)'"`UNIQ--ref-00000E94-QINU`"'
~6-8 hours'"`UNIQ--ref-0000001A-QINU`"'
~6-8 hours'"`UNIQ--ref-00000CF5-QINU`"'
~6.6 h
~60–80 h (memantine); ~70 h (donepezil)
~66 hours
~68 hours (terminal; reflects deep tissue accumulation, much longer than plasma)'"`UNIQ--ref-000003FC-QINU`"'
~7 days (euthyroid); longer in hypothyroidism (~9-10 days), shorter in hyperthyroidism'"`UNIQ--ref-00000036-QINU`"'
~7 hours
~7 hours (parent); ~9 hours (active AR-C124910XX metabolite, accounts for ~30-40% of activity)'"`UNIQ--ref-00000C92-QINU`"'
~7 hours apparent'"`UNIQ--ref-00001374-QINU`"'
~7 hours'"`UNIQ--ref-0000126E-QINU`"'
~7-10 hours (variable; longer in renal impairment)'"`UNIQ--ref-00000FB4-QINU`"'
~7-12 hours
~7.1 hours
~7.8 hours (fluticasone propionate, inhaled systemic exposure)'"`UNIQ--ref-000001DD-QINU`"'
~70 hours (long, supports once-daily dosing without peak-trough variation)'"`UNIQ--ref-0000001B-QINU`"'
~75 hours (long, accumulates over weeks)'"`UNIQ--ref-00000023-QINU`"'
~8 hours (longer in elderly and renal impairment)'"`UNIQ--ref-00000954-QINU`"'
~8 hours (parent); ~28 hours (desloratadine, the active metabolite, marketed separately as Clarinex)'"`UNIQ--ref-00000621-QINU`"'
~8 hours (shorter than suvorexant and lemborexant)
~8 hours'"`UNIQ--ref-000013F5-QINU`"'
~8-27 hours (highly variable across the population)'"`UNIQ--ref-00000A91-QINU`"'
~80 minutes SC'"`UNIQ--ref-000005F2-QINU`"'
~89 hours (EPA, the active metabolite)'"`UNIQ--ref-000013D1-QINU`"'
~9 hours (terminal)
~9 hours'"`UNIQ--ref-000014C3-QINU`"'
~9-14 hours'"`UNIQ--ref-00000FD2-QINU`"'
~91 hours
Search
bioavailability:
None
(417)
·
~50-60% (oral; substantial first-pass metabolism)'"`UNIQ--ref-0000002A-QINU`"' (1)
pregnancy:
None
(416)
·
Avoid from 20 weeks gestation onward per FDA's 2020 expanded NSAID warning (fetal renal dysfunction, oligohydramnios); contraindicated from 30 weeks (risk of premature ductus arteriosus closure)'"`UNIQ--ref-0000002B-QINU`"' (1)
·
Category C (per Desoxyn label) (1)
legal:
None
(411)
·
5-MeO-DMT is Schedule I in US (since 2011); the toad itself is protected in several southwestern states (1)
·
Currently legal in most jurisdictions with thujone limits (1)
·
Leaves legal in Bolivia, Peru, Colombia; cocaine internationally controlled (1)
·
Plant unrestricted; pharmaceutical atropine Rx-only (1)
·
Schedule I in US since 1993 (despite traditional use elsewhere); legal in Ethiopia, Kenya, Yemen, Somalia, Djibouti (1)
·
Schedule II (1)
·
[[USLegal:Prescription only|Rx-only]] for oral and most topical formulations in US; Voltaren Arthritis Pain 1% gel switched to [[USLegal:Over-the-counter|OTC]] in 2020 (1)
Error in "where" parameter: the string "--" cannot be used within #cargo_query.
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Drilldown: Medicines
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