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.
Coded indicator of the product.
β-Methylphenylethylamine is not approved for use in humans. Quantities of BMPEA in products purchased in 2014 were previously reported.1
1,3-Dimethylamylamine is a 1940s to 1960s nasal decongestant (Eli Lilly & Co) that was withdrawn from the market in the 1970s.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.
1,3-Dimethylbutylamine is not approved for use in humans.
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.
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.
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.