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Talk:Adderall

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Latest comment: 5 months ago by Diaxial in topic Line Model Enantiomers?
Good articleAdderall has been listed as one of the Natural sciences good articles under the good article criteria. If you can improve it further, please do so. If it no longer meets these criteria, you can reassess it.
Article milestones
DateProcessResult
December 3, 2014Good article nomineeListed


MAS title usage

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@Gobucks821 I've reverted the changes you made Re: substituting Adderall for "MAS products" throughout the article.

Adderall is the title of this article and the usage of Adderall to refer to the specific amphetamine salt composition in both Adderall and Mydayis dosage formulations is underpinned by previous consensus on this article's talk page. Moreover, the note in the title sentence of this article clarifies the usage of Adderall throughout the article.

For those reasons, in future you need to gain consensus on this article's talk page before making a change like that. Professional Crastination (talk) 05:02, 7 August 2024 (UTC)Reply

Contra TAAR1 agonism as the mediator of amphetamine actions

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Requesting input on this topic here at WikiProject Pharmacology. Thanks. – AlyInWikiWonderland (talk, contribs) 16:00, 13 December 2024 (UTC)Reply

Why I added [citation needed]

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Hello,

I hope I'm doing this correctly! I am new to editing and trying my best to follow all guidelines. I just added a citation needed tag to the following sentence: "The levoamphetamine component of Adderall has been reported to improve the treatment response in some individuals relative to dextroamphetamine alone."

I added this because there is no robust evidence for this claim -- and "has been reported" is, in my humble opinion, vague and dubious. Adderall is a direct remnant of Obetrol, which is an antiquated anti-obesity medication. Obetrol hails from the era where pharmaceutical companies would simply combine several controlled substances and test the result (example). I.e., Adderall's specific 3:1 combination of amphetamine salts is -- particularly in the context of being indicated for ADHD -- an arbitrary fluke, rising to the status of a first-line ADHD treatment principally for monetary reasons (as it is simply the latter formulation of Obetrol rebranded). Not to be presumptuous, but I may also add a dubious tag. I hope this clarifies my reasoning, and please let me know if additional clarification on my part is needed. Thank you. 173.169.248.124 (talk) 02:01, 24 December 2024 (UTC)Reply

Update: Decided on [weasel words] instead of dubious for "has been reported to".

Update 2: Changed "re-patented" (erroneous) to "rebranded" and clarified that it is a rebranded version of the latter/last formulation of Obetrol. I would also like to clarify that although the information is readily available, I am going to avoid -- out of an abundance of caution -- mentioning any specific pharmaceutical company as a new editor.

Dextroamphetamine Sulfate vs Amphetamine Sulfate

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Hello,

I will preface this saying that I have very little experience with chemistry, let alone with pharmacology.

The salt mixture is listed as:

   amphetamine apartate monohydrate 25% - stimulant (12.5% levo; 12.5% dextro)
   amphetamine sulfate 25% - stimulant (12.5% levo; 12.5% dextro)
   dextroamphetamine saccharate 25% - stimulant (0% levo; 25% dextro)
   dextroamphetamine sulfate 25% - stimulant (0% levo; 25% dextro)

Wouldn't it be clearer and, in my opinion, more accurate to list the salt mixture as:

   amphetamine apartate monohydrate 25% - stimulant (12.5% levo; 12.5% dextro)
   amphetamine sulfate 50% - stimulant (12.5% levo; 37.5% dextro)
   dextroamphetamine saccharate 25% - stimulant (0% levo; 25% dextro)

Dextroampetamine sulfate is just the right-handed form of amphetamine sulfate, right? Minnie1089 (talk) 08:41, 24 June 2025 (UTC)Reply

In Canada ...

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... Adderall is being marketed as "President's Choice" ;-)  Preceding unsigned comment added by 2A02:A03F:69A2:FA01:DC30:5617:3773:94D3 (talk) 11:07, 20 October 2025 (UTC)Reply

Line Model Enantiomers?

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Would it be useful to include line model images of the enantiomers ? Diaxial [talk] 11:43, 7 February 2026 (UTC)Reply