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Medicines (732)

Medicines > classes

: Antipsychotic

or Sedative-Hypnotic

or Stimulant

Use the filters below to narrow your results.

Other values:

None (51)

GABAA positive allosteric modulator (15) · Monoamine releasing agent (8) · Dopamine/norepinephrine reuptake inhibitor (5) · Phenothiazine D2 antagonist (5) · GABAA positive allosteric modulator (non-benzodiazepine) (3) · None (2) · Cathinone analogue; monoamine reuptake inhibitor (2) · Dopamine and norepinephrine reuptake inhibitor (2) · GABAA potentiator and direct activator (2) · Melatonin receptor agonist (2) · Norepinephrine–dopamine reuptake inhibitor (2)

Other values:

None (89) · No approved medical problem. Encountered as a designer/research benzodiazepine and, increasingly, as an adulterant in illicit opioid supplies. (1)

None (89) · No medical dose. Active recreational doses reported in the 0.5–1.5 mg range (similar potency to alprazolam). (1)

None (89) · Illicit tablets ("bars"), powders, blotter, occasionally solutions. No pharmaceutical product exists. (1)

None (89) · N/A (never approved) (1)

None (89) · intranasal; rectal and IV reported. (1) · Oral (1) · sublingual (1)

None (89) · ~20–40 min PO; faster sublingual/intranasal. (1)

None (89) · 6–10 h subjective; full pharmacologic effect considerably longer. (1)

None (89) · Estimated ~12–17 h (some sources cite up to ~21 h); active metabolites prolong effect. (1)

None (89) · Not formally characterized in humans. (1)

None (89) · 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)

None (90)

Showing below up to 90 results in range #1 to #90.

2

3

4

A

B

C

D

E

F

G

H

Hexedrone

I

L

M

N

N-Ethylhexedrone

P

Q

Quazepam

R

S

Secobarbital

T

Z

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