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🔗 MergedComparePsychonautWikiPharmacologyDrugCentral

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Classification
Class / category
Also known as
Haldol
Safety
Toxicity
can have serious side effects at higher dosagesrisk of having severe extrapyramidal symptoms and muscle rigidity
Dose · Oral
Threshold0.25 mg
Light0.25–1 mg
Common1–5 mg
Strong5–10 mg
Heavy10 mg+
Duration
Onset30–60 minutes
Total12–36 hours
Pharmacology
Receptor activity
D(2) dopamine receptorD(3) dopamine receptorD(4) dopamine receptorD(1A) dopamine receptor
HTR1DHTR2AHtr7DRD2DRD3DRD4Kcnj6KCNH1EBPHTR1AHTR1BHTR1EHTR1FHTR2BHTR2CHTR5AHTR6Ap2s1Adcy1Adra2bADRA1AADRA1BADRA1DADRA2AADRA2CADRB2ERG2CALM1DRD1DRD5HRH1HRH2H1F0Pgrmc1OPRM1ABCB1Chrm1Chrm2CHRM3CHRM5Oprd1polKCNK2KCNH2proteaseTmem97SIGMAR1SCN1ASLC6A2SLC6A4NETSlc18a3ZNF664
Half-lifeFollowing oral administration, the half-life was found to be 14.5-36.7 hours. Following intramuscular injection, mean half-life was found to be 20.7 hours. 10 MG Haloperidol IV and oral administration to healthy volunteers: serum T1/2 10-19 hr after IV and 12-38.3 hr after oral administration. Bioavailability in the order of 60%; distribution volume around 1300 L. Haloperidol, Elimination: Oral: 24 hours (range 12 to 37 hours). Intramuscular: 21 hours (range, 17 to 25 hours). Intravenous: 14 hours (range, 10 to 19 hours). Haloperidol decanoate, Elimination: Approximately 3 weeks (single or multiple doses).
Protein bindingStudies have found that free fraction of haloperidol in human plasma is 7.5-11.6%. This was found to be comparable among healthy adults, young adults, elderly patients with schizophrenia, and even in patients with liver cirrhosis.

Fact-sheets from PsychonautWiki. Harm-reduction reference only — not medical advice.