Treat fulvestrant as the answer to the limitations of the SERM class. SERMs such as tamoxifen are mixed agonist-antagonists, retaining estrogenic effects on endometrium and clotting; fulvestrant instead binds, fully blocks and then degrades the receptor, so it is correctly called a pure anti-estrogen and lacks those agonist liabilities. Clinically it is reserved for advanced hormone-positive breast cancer, and because it is not orally usable it is formulated as a depot intramuscular shot given about once a month, giving it a long, not short, duration. The claim that it is slower acting, shorter acting and less safe than SERMs contradicts both its depot pharmacology and its cleaner agonist-free profile, so that is the untrue statement.
\[\boxed{\text{Slower acting, shorter duration, lower safety profile than SERM}}\]