Botanical

Yohimbine

Also called yohimbe, yohimbe bark, yohimbine HCl, yohimbine hydrochloride, Pausinystalia johimbe, johimbi

By Kymata Labs EditorialMedical review pendingLast reviewed October 13, 2026 · What changed

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Summary

Yohimbine is the main alkaloid in yohimbe bark and a prescription drug in some countries. Small, mostly old trials of prescription yohimbine HCl found more erectile improvement than placebo; fat-loss trials are tiny and mixed. It is absorbed and cleared fast but very unevenly between people, and poison-centre reports link supplements to fast heartbeat, anxiety and high blood pressure.

Top graded outcomes:C evidence grade Erectile function in men with erectile dysfunctionD evidence grade Weight loss on a low-calorie diet in women with obesityD evidence grade Body fat in professional soccer players

Key facts

Safety first
Associated with irregular heartbeat, blood-pressure problems, heart attacks and seizures; restricted or banned in many countries[10]
Same dose, very different exposure
In CYP2D6 poor metabolisers, a 5 mg dose gave about 126 times the blood exposure (AUC 2,044 vs 16.2 ng·h/mL) and a 6.6 h vs 0.64 h half-life compared with extensive metabolisers[18]
Absorption
Oral bioavailability ranged from 7% to 87% (mean 33%) in 7 men; a later study measured 22.3 ± 21.5%[6][16]
Speed
After 10 mg by mouth: absorption half-time 0.17 h (about 10 minutes) and elimination half-life 0.60 ± 0.26 h in 8 men[13]
Poison-centre data
238 California cases (2000-2006): stomach upset 46%, fast heartbeat 43%, anxiety or agitation 33%, high blood pressure 25%; 98.7% involved supplement products[8]
Label accuracy
Of 49 US supplements, only 11 listed a yohimbine amount and most of those were wrong (23% to 147% of the label); content ranged from none to 12.1 mg per serving[7]
Main trial evidence
Meta-analysis of 8 RCTs of prescription yohimbine HCl for erectile dysfunction: pooled odds of erectile improvement 2.87 times placebo (7 trials reported this outcome); yohimbine alone OR 2.08[2]
Fat-loss trials
Three small trials: more weight loss on a diet (n=20, 3 weeks), lower body fat in soccer players (n=20, 21 days), and no effect on weight or body fat over 6 months (n=33)[21][3][22]
Drug interactions
Not for people on MAO-inhibitor or tricyclic antidepressants (NIH fact sheet); a case of brain haemorrhage occurred in a woman on clonidine[10][9]
Evidence base
5 graded human outcomes on this page
Last reviewed
October 13, 2026

How it works

EstablishedYohimbine blocks alpha-2 adrenergic receptors, which normally brake noradrenaline release, so sympathetic output rises: noradrenaline, heart rate and blood pressure go up. Fat cells also carry alpha-2 receptors that restrain fat breakdown, which is the rationale for fat-loss use. Its main metabolite, 11-hydroxy-yohimbine, also blocks alpha-2 receptors in human cell tests.[11][14][17][4][20][28]

What the human research says

Human trials only, one row per outcome. The form column shows what each trial actually tested. Grades follow our evidence-grading policy.

At a glance: strongest evidence per outcome

Evidence at a glance: strongest human evidence per outcome
OutcomeGradeEffectStrongest evidenceRows
Erectile functionGrade CImprovedOR 2.87 vs placeboMeta-analysis of 8 trials · n = 460 · 2021Form tested: Prescription yohimbine HCl alone or combined with L-arginine or trazodone1 row
Body weight & fatGrade DNo effectNo differenceRCT · n = 33 · 1991Form tested: Yohimbine3 rows
Exercise performanceGrade DImprovedCrossover RCT · n = 18 · 2022Form tested: Yohimbine HCl1 row

Every graded row

Outcome
Grade
Form tested
Sort

Showing 5 of 5 outcomes. Human trials only.

OutcomeEffectGradeBest evidencePMID
Erectile function in men with erectile dysfunctionImprovedGrade C

Meta-analysis · n = 460 · 2021

Men aged 18-73 with erectile dysfunction of mixed causes in 8 double-blind RCTs (1987-2010)

Form: Prescription yohimbine HCl alone or combined with L-arginine or trazodone · Dose: Mostly 5.4-6 mg three or four times daily; one trial used 100 mg/day · Duration: 2-10 weeks

Erectile improvement was more likely than with placebo (OR 2.87, 95% CI 1.94-4.25); yohimbine alone OR 2.08. Overall sexual function did not differ significantly with yohimbine alone (P = .07).

35118966 (opens PubMed)Source [2]
Body weight, body fat and fat distribution in menNo effectGrade D

RCT · n = 33 · 1991

Men, mean age 42 (USA); 47 randomised, 33 completed

Form: Yohimbine · Dose: High dose, titrated to a peak of 43 mg/day · Duration: 6 months

No effect versus placebo on body weight, BMI, total or HDL cholesterol, body fat, waist-to-hip ratio or CT-measured fat distribution.

1960007 (opens PubMed)Source [22]
Weight loss on a low-calorie diet in women with obesityImprovedGrade D

RCT · n = 20 · 1991

Female outpatients with obesity (Poland), after a 3-week 1,000 kcal/day run-in diet

Form: Yohimbine tablets · Dose: 5 mg four times daily (20 mg/day) · Duration: 3 weeks (with a 1,000 kcal/day diet)

Weight loss was 3.55 ± 0.24 kg with yohimbine vs 2.21 ± 0.37 kg with placebo (P < 0.005). Serum glycerol, the lipolysis marker, did not change significantly.

1955308 (opens PubMed)Source [21]
Body fat in professional soccer playersImprovedGrade D

RCT · n = 20 · 2006

Elite male soccer players in Serbia

Form: Yohimbine tablets · Dose: 20 mg/day in two doses · Duration: 21 days

Body fat fell from 9.3% to 7.1% with yohimbine; body mass, muscle mass and all performance tests did not change. No side effects were reported.

17214405 (opens PubMed)Source [3]
Repeated sprint power in active womenImprovedGrade D

Crossover RCT · n = 18 · 2022

Physically active women (USA)

Form: Yohimbine HCl · Dose: 2.5 mg single dose 20 min before exercise · Duration: Single session

Mean power and total work over 3 x 15 s Wingate sprints were higher and fatigue index and lactate lower than placebo; adrenaline and heart rate rose.

35162339 (opens PubMed)Source [4]

Forms

FormElemental %Absorption (human data)GI toleranceStudied for
Yohimbine HCl (prescription and supplement tablets)Varies[6]Not applicable (whole compound or extract; no elemental fraction)Absorbed fast (absorption half-time 0.17 h after 10 mg) and usually cleared fast (half-life about 0.6 h), but oral bioavailability ranged from 7% to 87% (mean 33%). A high-fat meal reduced both the rate and extent of absorption.[13][6][19]Side effects reported to poison centres: stomach upset, fast heartbeat, anxiety, high blood pressure. 5.4 mg yohimbine HCl contains about 4.9 mg yohimbine base.[8][38]Erectile dysfunction trials (about 15–22 mg/day), fat-loss trials (20–43 mg/day) and small sports studies (2.5–20 mg/day)
Yohimbe bark extractVaries[7]Not applicable (whole compound or extract; no elemental fraction)No human pharmacokinetic data for bark extracts; analysed products ranged from no detectable yohimbine to 12.1 mg per serving.[7]Label amounts are unreliable, so the actual dose is often unknown.[7][10]Not tested in controlled human trials
Rauwolscine (alpha-yohimbine)Varies[37]Not applicable (whole compound or extract; no elemental fraction)A stereoisomer of yohimbine (same formula, different 3D shape), not the same molecule. We found no human pharmacokinetic studies.[37]Not characterised in controlled human studies; it is one of the alkaloids measured in yohimbe products.[7][37]No controlled human supplement trials found (PubMed search, October 2026)

Studied doses

Doses studied in human trials ranged from a single 2.5 mg dose before exercise to 20 mg/day in the short fat-loss trials (5 mg four times daily, or 10 mg twice daily) and about 15–22 mg/day of prescription yohimbine HCl in most erectile dysfunction trials. Single oral doses up to 21.6 mg were given in pharmacology studies, a 6-day safety study went up to 16.2 mg three times daily, a 6-month trial titrated up to 43 mg/day, and one erectile trial used 100 mg/day. A lipolysis study dosed by body weight (0.2 mg/kg, about 14 mg at 70 kg). These are doses researchers used, not targets, and the same dose produced very different blood levels in different people.[4][21][3][2][19][15][22][20][18]

These are amounts used in research, not personal advice. Your clinician or pharmacist can say what fits you.

How long trials ran before effects were measured

When each outcome was assessed in the cited trials. It is not a promise of when anyone will notice a change.

Blood levels
Within about 20–25 minutes in most people · Absorption half-time 0.17 h after 10 mg; time to peak 0.36 h in CYP2D6 extensive metabolisers but about 1.4 h in poor metabolisers after 5 mg[13][18]
Noradrenaline
Within 15 minutes (intravenous) · Plasma noradrenaline tripled within 15 minutes of 0.25–0.5 mg/kg intravenously[14]
Standing blood pressure (autonomic failure)
Measured at 60 minutes · Standing diastolic pressure up 11 mm Hg 60 minutes after 5.4 mg[5]
Sprint power
Dose given 20 minutes before exercise · Single 2.5 mg dose before 3 × 15 s sprints[4]
Body weight or fat
3 weeks in two small trials; no effect at 6 months · Diet trial in women and soccer-player trial at 20 mg/day; 6-month trial in men up to 43 mg/day[21][3][22]
Erectile function
2–10 weeks · Trial lengths in the 2021 meta-analysis[2]

Interactions

Published interactions only: each row cites a source. No row means none was found in our sources, not that a combination is safe.

Medicines

  • MAO-inhibitor and tricyclic antidepressantsNIH fact sheete.g. Phenelzine, tranylcypromine, amitriptyline, nortriptylineThe NIH fact sheet says not to use yohimbe with these antidepressants because of interactions.[10]
  • SSRIs and other CYP2D6 inhibitorsPK studye.g. Paroxetine, fluoxetine, bupropionYohimbine is cleared mainly by CYP2D6 (an estimated 99.5% of clearance in a 2020 trial). Paroxetine 20 mg cut yohimbine clearance more than fivefold in extensive metabolisers; other strong CYP2D6 inhibitors would be expected to act similarly (inferred). The Yocon label says it should not be combined with antidepressants or other mood-modifying drugs.[18][31]
  • Clonidine and other centrally acting blood-pressure drugsCase reporte.g. Clonidine, guanfacineA woman on long-term clonidine (also taking bupropion and desvenlafaxine) had blood pressure of 198/93 and a basal-ganglia haemorrhage after a yohimbine-labelled supplement; authors note clonidine use may amplify yohimbine effects.[9]
  • Blood-pressure-lowering medicinesRCTe.g. Any antihypertensiveYohimbine raises blood pressure: 10 mg raised diastolic pressure in people with untreated hypertension but not in healthy volunteers, 5.4 mg raised standing diastolic pressure by 11 mm Hg in autonomic failure, and high blood pressure was reported in 25% of poison-centre cases.[29][5][8]
  • Caffeine, pre-workouts and other stimulantsReviewe.g. Caffeine, synephrine; also bupropion and desvenlafaxine, which raise noradrenalineNo controlled trial has tested yohimbine with caffeine; a 2002 hypothesis paper only proposed that the pairing be studied. Stimulant supplements including yohimbine are linked to tachycardia, hypertension and cardiac events, and in the haemorrhage case the authors suggest bupropion and desvenlafaxine likely worsened the reaction.[30][12][9]

Who should be careful

Heart disease, high blood pressure or arrhythmia
Yohimbine has been associated with irregular heartbeat, blood-pressure problems, heart attacks and seizures, and raised diastolic pressure in people with untreated hypertension.[10][32][29]
Panic disorder, PTSD and anxiety
Researchers use yohimbine to provoke anxiety: it triggered panic attacks in 37 of 68 people with panic disorder or agoraphobia with panic attacks (1 of 20 healthy volunteers), and intravenous yohimbine triggered panic attacks in 14 of 20 men with PTSD.[23][24]
Other psychiatric conditions
The Yocon prescribing information says it is not intended for psychiatric patients in general or for use with mood-modifying drugs.[31]
Kidney or liver disease
Kidney disease is the listed contraindication on the Yocon label, and Health Canada warns of serious reactions in people with kidney or liver disease. Yohimbine is cleared mainly by liver metabolism.[31][32][13]
Pregnancy, breastfeeding and children
The NIH fact sheet says oral yohimbe might be unsafe in pregnancy or while breastfeeding; Health Canada says it should not be used by pregnant or nursing women or children.[10][32]
People on antidepressants or clonidine-type drugs
MAO-inhibitor and tricyclic antidepressants should not be combined with yohimbe, paroxetine sharply raised yohimbine levels, and a clonidine user had a brain haemorrhage after a dose.[10][18][9]

Talk to your pharmacist or clinician before starting a supplement, especially if you take prescription medicines.

Safety first

The risks are better documented than the benefits.

Poison-centre reports
California poison centre cases rose from 1.8 to 8.0 per 10,000 adult exposures between 2000 and 2006, and yohimbine cases were more likely to have severe outcomes (OR 5.81) than average exposures.[8]
Labels you cannot trust
Only 2 of 49 US products gave both an accurate yohimbine amount and side-effect information.[7]
Legal status
US: selling an over-the-counter yohimbine product as an erectile dysfunction remedy without FDA approval is illegal. Canada: yohimbine and its salts are on the Prescription Drug List. Australia: yohimbine is prescription-only. EU: yohimbe bark and its preparations have been prohibited in food since 2019. UK: herbal medicines containing yohimbe bark may be sold only in registered pharmacies.[10][33][34][35][36]
Variable absorption
Bioavailability ranged from 7% to 87% between people, and in four people hospitalised after a drug powder, all assumed to have taken the same dose, blood levels differed 22-fold (249–5,631 ng/mL); modelling showed CYP2D6 differences could explain the spread.[6][26]

How the body handles yohimbine

Fast in, fast out for most people, with large exceptions.

Absorption and half-life
After a single 10 mg oral dose in 8 men, the absorption half-time was 0.17 ± 0.11 h and the elimination half-life 0.60 ± 0.26 h; almost none (0.35%) left unchanged in urine, so clearance is by metabolism.[13]
Bioavailability
With 10 mg oral vs intravenous doses in 7 men, oral bioavailability ranged from 7% to 87% (mean 33%); a later study found 22.3 ± 21.5%. The authors note dosing may need individualising.[6][16]
Intravenous data
After 0.25–0.5 mg/kg intravenously in 13 men, elimination half-life ranged from 0.25 to 2.5 h and plasma noradrenaline tripled within 15 minutes, while adrenaline did not change.[14]
Repeated dosing
Over 6 days at 5.4–16.2 mg three times daily or 21.6 mg twice daily (32 volunteers), there was no drug accumulation but large differences within and between people; catecholamines rose with blood levels.[15]
Active metabolite
The main metabolite, 11-hydroxy-yohimbine, blocks alpha-2 receptors in human cell tests and has a terminal half-life almost four times that of yohimbine (347 vs 91 minutes after intravenous dosing).[28][16]
CYP2D6 genetics
In 172 people, conversion to 11-hydroxy-yohimbine varied more than 1,000-fold and 17 showed none, with CYP2D6 the likely main route. In a 2020 trial, poor metabolisers had about 126 times the exposure of extensive metabolisers after 5 mg; about 10% of people of European ancestry are poor metabolisers.[17][18]

Fasted or with food?

Food appears to trade a softer peak for less fat mobilisation.

Food slows absorption
In single-dose studies up to 21.6 mg, a high-fat meal reduced both the rate and the extent of yohimbine absorption. The abstract gives no percentage, and we found no published figure for how much.[19]
Food cancels the fat-mobilising effect
0.2 mg/kg by mouth raised blood glycerol and free fatty acids in fasting men; the effect was stronger during exercise and completely suppressed after a meal.[20]
The trade-off
A slower, smaller peak might mean fewer jitters, though no study measured that; but the meal study suggests food also removes the lipolysis that is the reason for fasted use. Higher blood levels went with larger rises in blood pressure and breathing rate.[19][20]

Pre-workout and fasted cardio

An anecdotal community practice that has not been tested for fat loss.

Practice, not evidence
Using yohimbine before fasted cardio is an anecdotal practice in fitness communities; no study has measured how common it is. It rests on a 1988 study of blood fat markers and a 2002 hypothesis paper, not on trials measuring fat loss from that routine.[20][30]
What exercise trials measured
A single 2.5 mg dose 20 minutes before sprints raised mean power and heart rate in 18 women; 20 mg/day for 21 days lowered body fat in 20 soccer players but did not change performance tests.[4][3]
Stacking with caffeine or stimulants
No trial has tested the combination. Stimulant supplements including yohimbine are linked to tachycardia, high blood pressure and cardiac events; stimulant effects were a reason for use in 7.6% of California poison-centre cases.[30][12][8]

Serious reactions on record

Common complaints
Health Canada lists anxiety and frequent urination as the most consistent side effects, plus dizziness, stomach upset, headache, sweating, insomnia, tremor, palpitations and severe hypertension; the Yocon label adds irritability.[32][31]
Priapism
A man needed surgery (a cavernosal shunt) for a prolonged erection after a yohimbe extract product.[25]
Brain haemorrhage
A 39-year-old woman on clonidine had blood pressure of 198/93 and a basal-ganglia haemorrhage after a yohimbine-labelled supplement; product content was not tested.[9]
Deaths
Two US medical examiner cases attributed death to acute yohimbine intoxication, with blood levels of 7,400 and 5,400 ng/mL.[27]

How to read the label

  1. Yohimbine vs yohimbeTrials used measured yohimbine HCl; many products list only yohimbe bark, with no yohimbine amount.[7][2]
  2. Label errorsWhere a yohimbine amount was listed, actual content ranged from 23% to 147% of the label.[7]
  3. Bark extract is not a yohimbine amountA bark-extract weight on the label says nothing about yohimbine content; analysed products ranged from none detected to 12.1 mg of yohimbine per serving.[7]
  4. Rauwolscine and alpha-yohimbineThese names refer to a stereoisomer of yohimbine, a different compound; we found no controlled human trials of it, and yohimbine data do not transfer to it.[37]
  5. Salt vs basePrescription tablets state yohimbine hydrochloride; about 90.7% of that weight is yohimbine itself (354.4 ÷ 390.9).[38][31]

Frequently asked questions

Is yohimbine the same as yohimbe or rauwolscine?

No. Yohimbine is one alkaloid in yohimbe bark, and bark products often do not say how much they contain. Rauwolscine (alpha-yohimbine) is a stereoisomer of yohimbine, a different compound with no controlled human trials.[7][10][37]

Does yohimbine work for erectile dysfunction?

Older trials of prescription yohimbine HCl found erectile improvement more often than placebo, but the trials were small and mostly decades old.[2]

Does yohimbine burn fat?

Evidence is thin and mixed. Two 3-week trials of 20 people found more weight loss on a diet or lower body fat with 20 mg/day; a 6-month trial in 33 men up to 43 mg/day found no effect on weight or body fat.[21][3][22]

Does food change how yohimbine works?

Yes. A high-fat meal slowed and reduced absorption, and a meal completely suppressed the rise in blood fat markers seen when fasting. Food may soften the peak, but it also seems to remove the effect people use it for. No study gives a precise percentage.[19][20]

Is yohimbine before fasted cardio evidence-based?

No. It is an anecdotal community practice built on a 1988 study of blood fat markers and a 2002 hypothesis paper; no trial has measured fat loss from that routine. Adding caffeine or other stimulants has not been tested, and stimulant supplements including yohimbine are linked to fast heartbeat and high blood pressure.[20][30][12]

Why do people react so differently to the same dose?

Absorption varies from 7% to 87%, and CYP2D6 genes control clearance: poor metabolisers had about 126 times the exposure after 5 mg. CYP2D6-blocking drugs such as paroxetine have a similar effect.[6][18]

What are the main side effects?

Stomach upset, fast heartbeat, anxiety or agitation and high blood pressure were the most common problems reported to a poison centre. Insomnia, tremor and frequent urination are also reported, and it can trigger panic attacks in people with panic disorder or PTSD.[8][32][23][24]

Is yohimbine legal?

It depends on the country. Yohimbine is prescription-only in Canada and Australia, yohimbe is prohibited in food in the EU, and in the UK herbal yohimbe medicines are pharmacy-only. In the US yohimbe is sold as a supplement, but not legally as an erectile dysfunction remedy without FDA approval.[33][34][35][36][10]

Sources

  1. [1]Yohimbine for erectile dysfunction: a systematic review and meta-analysis of randomized clinical trials.. J Urol, 1998. meta-analysis PMID 9649257
  2. [2]Yohimbine as a treatment for erectile dysfunction: A systematic review and meta-analysis.. Turk J Urol, 2021. meta-analysis PMID 35118966
  3. [3]Yohimbine: the effects on body composition and exercise performance in soccer players.. Res Sports Med, 2006. RCT PMID 17214405
  4. [4]Effects of Acute Yohimbine Hydrochloride Supplementation on Repeated Supramaximal Sprint Performance.. Int J Environ Res Public Health, 2022. crossover-RCT PMID 35162339
  5. [5]Comparative efficacy of yohimbine against pyridostigmine for the treatment of orthostatic hypotension in autonomic failure.. Hypertension, 2010. crossover-RCT PMID 20837887
  6. [6]Yohimbine bioavailability in humans.. Eur J Clin Pharmacol, 1990. PK-study PMID 2076728
  7. [7]Pharmaceutical quantities of yohimbine found in dietary supplements in the USA.. Drug Test Anal, 2016. observational PMID 26391406
  8. [8]Adverse drug events associated with yohimbine-containing products: a retrospective review of the California Poison Control System reported cases.. Ann Pharmacother, 2010. observational PMID 20442348
  9. [9]Intracranial hemorrhage after a single dose of Yohimbine in a chronic user of clonidine.. Am J Emerg Med, 2022. observational PMID 36115742
  10. [10]Yohimbe: Usefulness and Safety. National Center for Complementary and Integrative Health (NIH), 2025. fact-sheet
  11. [11]Multifaced Nature of Yohimbine-A Promising Therapeutic Potential or a Risk?. Int J Mol Sci, 2024. review PMID 39684567
  12. [12]Cardiovascular toxicity associated with supplement use.. Clin Toxicol (Phila), 2025. review PMID 40960841
  13. [13]The pharmacokinetics of yohimbine in man.. Eur J Clin Pharmacol, 1987. PK-study PMID 3653227
  14. [14]Yohimbine pharmacokinetics and interaction with the sympathetic nervous system in normal volunteers.. Eur J Clin Pharmacol, 1992. PK-study PMID 1493849
  15. [15]Yohimbine elimination in normal volunteers is characterized by both one- and two-compartment behavior.. J Cardiovasc Pharmacol, 1997. PK-study PMID 9234649
  16. [16]Biopharmaceutics and metabolism of yohimbine in humans.. Eur J Pharm Sci, 1999. PK-study PMID 10494000
  17. [17]Human sympathetic activation by alpha2-adrenergic blockade with yohimbine: Bimodal, epistatic influence of cytochrome P450-mediated drug metabolism.. Clin Pharmacol Ther, 2004. PK-study PMID 15289791
  18. [18]Oral Yohimbine as a New Probe Drug to Predict CYP2D6 Activity: Results of a Fixed-Sequence Phase I Trial.. Clin Pharmacokinet, 2020. PK-study PMID 32060866
  19. [19]Effects of yohimbine on autonomic measures are determined by individual values for area under the concentration-time curve.. J Clin Pharmacol, 1996. PK-study PMID 8889902
  20. [20]Alpha 2-antagonist compounds and lipid mobilization: evidence for a lipid mobilizing effect of oral yohimbine in healthy male volunteers.. Eur J Clin Invest, 1988. RCT PMID 2906290
  21. [21]Does yohimbine act as a slimming drug?. Isr J Med Sci, 1991. RCT PMID 1955308
  22. [22]Yohimbine does not affect fat distribution in men.. Int J Obes, 1991. RCT PMID 1960007
  23. [23]Neurobiological mechanisms of panic anxiety: biochemical and behavioral correlates of yohimbine-induced panic attacks.. Am J Psychiatry, 1987. observational PMID 3037926
  24. [24]Abnormal noradrenergic function in posttraumatic stress disorder.. Arch Gen Psychiatry, 1993. observational PMID 8466387
  25. [25]Refractory priapism associated with ingestion of yohimbe extract.. J Med Toxicol, 2009. observational PMID 19876857
  26. [26]CYP2D6 phenotype explains reported yohimbine concentrations in four severe acute intoxications.. Arch Toxicol, 2021. observational PMID 34027562
  27. [27]Case study: two fatal case reports of acute yohimbine intoxication.. J Anal Toxicol, 2013. observational PMID 23846025
  28. [28]Alpha 2-adrenoceptor antagonist potencies of two hydroxylated metabolites of yohimbine.. Br J Pharmacol (laboratory study in human platelets and fat cells), 1993. animal-study PMID 8097957
  29. [29]Yohimbine effects on blood pressure and plasma catecholamines in human hypertension.. Am J Hypertens, 1995. RCT PMID 7662240
  30. [30]Pre-exercise administration of yohimbine may enhance the efficacy of exercise training as a fat loss strategy by boosting lipolysis.. Med Hypotheses, 2002. review PMID 12323115
  31. [31]Yocon (yohimbine hydrochloride) 5.4 mg tablets: prescribing information. Glenwood LLC, reproduced by RxList, 2008. label
  32. [32]Health Canada advises consumers not to use unapproved products containing yohimbine or yohimbe bark including Strauss Energy SIX capsules. Health Canada, 2006. safety-communication
  33. [33]Natural Health Products Ingredients Database: Yohimbine (non-NHP, listed in the Prescription Drug List). Health Canada, 2019. database
  34. [34]Erec-Bull tablets: safety advisory (undeclared yohimbine, a prescription-only substance in Australia). Therapeutic Goods Administration (Australia), 2014. safety-communication
  35. [35]Commission Regulation (EU) 2019/650 amending Annex III to Regulation (EC) No 1925/2006 as regards Yohimbe (Pausinystalia yohimbe). European Commission (Official Journal L 110), 2019. guideline
  36. [36]Banned and restricted herbal ingredients. Medicines and Healthcare products Regulatory Agency (UK), 2014. guideline
  37. [37]Rauwolscine (alpha-yohimbine), CID 643606. PubChem (NCBI), 2026. database
  38. [38]Yohimbine hydrochloride, CID 6169 (molecular weight 390.9) and yohimbine, CID 8969 (354.4). PubChem (NCBI), 2026. database

What changed

  1. October 13, 2026 · all · new pageInitial editorial evidence review: source titles and years taken from NCBI E-utilities esummary (no retraction or expression-of-concern flags), every evidence row, dose, n and duration read against the PubMed abstract or full text, funding and author affiliations checked where available, and grades held conservative.Writer: Kymata Labs Editorial · No credentialed reviewer yet
  2. October 13, 2026 · evidence, forms, doses, interactions, safety, timing, label, analysis, FAQ · evidence re-reviewEditorial evidence re-review: added pharmacokinetics (Owen 1987, Guthrie 1990, Hedner 1992, Sturgill 1997, Le Corre 1999 and 2004, Vay 2020), fasted vs fed (Grasing 1996, Galitzky 1988), two fat-loss trials (Kucio 1991, Sax 1991), panic and PTSD challenge data, priapism and fatal-case reports, CYP2D6 and stimulant interactions, rauwolscine, and verified regulatory status for the US, Canada, Australia, EU and UK. Every PMID checked via NCBI esummary and key numbers read against abstracts or full text; grades held conservative.Writer: Kymata Labs Editorial · No credentialed reviewer yet
  3. October 13, 2026 · safety, interactions, FAQ, sources · evidence re-reviewIndependent adversarial re-check: every PMID re-verified via NCBI esummary (titles and years match, no retraction flags), numbers re-read against abstracts and the 2020 CYP2D6 trial's tables, and regulatory pages re-opened. Softened the 2021 intoxication wording to match the paper (same dose assumed; CYP2D6 could explain the spread), labelled pre-workout use as anecdotal, removed an unsourced drug example from the stimulant interaction, and noted that the 1993 metabolite study used human cells in the lab.Writer: Kymata Labs Editorial · No credentialed reviewer yet

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