The Therapeutic Goods Administration (TGA) has made interim decisions to amend the Poisons Standard for Cytisine, Dextromethorphan, and Dihydrocodeine.
These decisions are based on considerations such as risks and benefits, toxicity, potential for abuse, and other public health matters. The TGA’s interim decisions are made after considering public submissions and the advice of the Advisory Committee on Medicines Scheduling (ACMS) or the Advisory Committee on Chemicals Scheduling (ACCS).
The committee’s decisions are based on subsection 52E(1) of the Act, which includes factors such as:
Region: Australia
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