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They are not for human consumption, not for medical or veterinary use, and not approved by the FDA or any regulatory authority

Drug development for indications is leaning towards precise classification, with therapies approved for rare cancers or tumors (including recurrent types) such as low-grade serous ovarian cancer, diffuse gliomas, acute myeloid leukemia, and non-small cell carcinoma with HER2 (ERBB2) activating mutations, all featuring entirely new mechanisms for approval

Patients with AFib who took lower doses of blood-thinning medications experienced more bleeding episodes in the first three months of treatment compared to those who took standard doses, according to a 2024 study in the Journal of Blood Advances

(2020) Arsenic toxicity: Molecular targets and therapeutic agents, Biomolecules, vol