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. 2018 Oct 22;178(12):1721–1723. doi: 10.1001/jamainternmed.2018.4846

Table. Quantities of 4 Experimental Stimulants Subject to FDA Public Notices in Supplements Purchased in 2014 and 2017.

Producta Claim on Label or Website BMPEA,b Mean (SD), mg per Pill or Capsule 1,3-DMAA,c Mean (SD), mg per Pill or Capsule DMBA,d Mean (SD), mg per Pill or Capsule Oxilofrine,e Mean (SD), mg per Pill or Capsule
Supplements Purchased in 2014
A Cognitive function ND ND ND 0.07 (0.04)
B Weight loss ND ND ND 54.31 (0.82)
C Weight loss 18.71 (2.16) 36.70 (11.91)f ND 34.07 (10.06)
D Weight loss 5.74 (1.15) ND ND 26.48 (2.56)
E Weight loss 27.35 (5.87) 34.68 (0.89)f ND 34.31 (2.06)
F Weight loss ND ND ND 0.31 (0.04)
G Sports supplement 3.22 (0.67) ND ND 7.78 (0.49)
H Sports supplement 31.23 (5.72) ND ND 31.07 (1.94)
I Weight loss 9.89 (1.26) 12.17 (1.23)f ND 25.62 (1.53)
J Weight loss 3.35 (0.74) 12.03 (1.31)f ND 37.45 (1.21)
K Weight loss 0.97 (0.31) 11.39 (1.74)f ND 40.75 (5.31)
L Weight loss 23.05 (2.79) 26.89 (6.05)f ND 37.44 (7.43)
Supplements Purchased in 2017
A Cognitive function ND ND ND 0.05 (0.01)f
B Weight loss ND ND ND 40.84 (6.48)f
C Weight loss ND ND 30.43 (3.26)f 7.09 (0.91)f
D Weight loss ND ND ND 28.38 (0.82)f
Eg Weight loss 17.23 (1.47)f 36.12 (5.45)f ND 27.43 (1.06)f
F Weight loss ND ND ND ND
G Sports supplement ND ND ND ND
H Sports supplement ND ND ND ND
I Weight loss ND ND 10.98 (3.09)f 5.59 (0.85)f
J Weight loss ND 27.99 (1.37)f ND 8.77 (0.47)f
K Weight loss ND ND 17.05 (1.63)f 8.44 (0.51)f
L Weight loss ND ND 39.53 (4.39)f 8.85 (0.81)f

Abbreviations: BMPEA, indicates β-methylphenylethylamine; DMBA, 1,3-dimethylbutylamine; 1,3-DMAA, 1,3-dimethylamylamine; FDA, US Food and Drug Administration; ND, not detectable.

a

Coded indicator of the product.

b

β-Methylphenylethylamine is not approved for use in humans. Quantities of BMPEA in products purchased in 2014 were previously reported.1

c

1,3-Dimethylamylamine is a 1940s to 1960s nasal decongestant (Eli Lilly & Co) that was withdrawn from the market in the 1970s. It was never approved for oral use.

d

1,3-Dimethylbutylamine is not approved for use in humans.

e

Oxilofrine was previously available in several European countries. It increased blood pressure and cardiac output and was available in 16- to 40-mg capsules. It was never approved for use in the United States.

f

Quantities represent stimulants in supplements after the FDA issued a public notice about the stimulant. The date of the FDA warning for 1,3-DMAA was July 2013; DMBA, April 2015; BMPEA, April 2015; and oxilofrine (referred to as methylsynephrine), April 2016.

g

Manufacturer of product E also received an FDA warning letter in 2015 that BMPEA was a prohibited ingredient listed on the label of product E.