Teva has moved to reassure US patients after trending videos on the social media platform TikTok doubted the efficacy of the renowned, shortage-hit treatment for attention deficit hyperactivity disorder, Adderall (mixed amphetamine salts), and its AB-rated generic equivalents.
Teva Offers Reassurance After TikTok Adderall Efficacy Claims
Videos Of Alleged Adderall Patients Stating Medication ‘Isn’t Working’ Go Viral
Teva, one of the largest manufacturers and suppliers of branded and generic Adderall, the renowned treatment for ADHD and narcolepsy, has responded to claims.

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Bringing in sales that translated to nearly $1.5bn last year, Japan’s Towa was feeling upbeat after a challenging few years, both for itself and the broader Japanese generics market. However, its financial guide for the next 12 months has left investors feeling cold.
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Henlius has reported progress in its development of a bevacizumab product for treating ophthalmic diseases, with its Essex-partnered HLX04-O candidate meeting its primary endpoint in a Phase III trial. Meanwhile, Outlook Therapeutics has taken another shot at getting its own ophthalmic bevacizumab approved in the US after resubmitting its filing.
With sales of $550m last year and a high barrier to entry, Exparel marks an intriguing target for abbreviated new drug application sponsors. Having shot down a US patent last year and won US FDA approval for its ANDA, Jiangsu Hengrui’s US eVenus Pharmaceutical Laboratories subsidiary and partner Fresenius Kabi have just reached a settlement agreement.
While the biosimilars industry has welcomed individual pockets of progress around regulatory streamlining, it is essential that approaches from global authorities move forward together if they are to have a meaningful impact on biosimilar development. At Medicines for Europe’s annual biosimilars conference, regulators from around the world talked about how their thinking is converging.