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Medicines > classes : Anticonvulsant or Classic Psychedelic or Sedative-hypnotic

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generic:
brand:
None (78)
classes: (Click arrow to add another value)
mechanism:
5-HT2A agonist (26) · GABAA positive allosteric modulator (16) · Potent 5-HT2A agonist (5) · LSD analogue; 5-HT2A agonist (4) · Prodrug of LSD; 5-HT2A agonist (4) · GABAA positive allosteric modulator (non-benzodiazepine) (3) · GABAA potentiator and direct activator (3) · None (2) · Contains LSA (2) · Contains mescaline (2) · Melatonin receptor agonist (2) · Sodium channel blocker (2)
uses:
None (118) · No approved medical problem. Encountered as a designer/research benzodiazepine and, increasingly, as an adulterant in illicit opioid supplies. (1)
starting dose:
None (118) · No medical dose. Active recreational doses reported in the 0.5–1.5 mg range (similar potency to alprazolam). (1)
preparations:
None (118) · Illicit tablets ("bars"), powders, blotter, occasionally solutions. No pharmaceutical product exists. (1)
fda max:
None (118) · N/A (never approved) (1)
routes:
None (117) · intranasal; rectal and IV reported. (1) · Oral (2) · sublingual (1)
onset:
None (117) · 30–60 minutes (1) · ~20–40 min PO; faster sublingual/intranasal. (1)
duration:
None (117) · 6–10 h subjective; full pharmacologic effect considerably longer. (1) · 8–12 hours (1)
halflife:
None (117) · 3–5 hours (1) · Estimated ~12–17 h (some sources cite up to ~21 h); active metabolites prolong effect. (1)
bioavailability:
None (117) · 70–90% (oral) (1) · Not formally characterized in humans. (1)
pregnancy:
None (117) · Avoid. Benzodiazepines are associated with neonatal sedation, floppy-infant syndrome, and withdrawal; teratogenic signal weak but non-zero. Designer benzo with no safety data, assume worst-case. (1) · Not established (1)
legal:
None (118) · Schedule I (United States) (1)

Showing below up to 119 results in range #1 to #119.

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