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Instead, they often peaked during titration and then levelled off, meaning that once participants were settled into their maintenance schedule, side effects tended to diminish rather than worsen

The documentation should reflect the clinical reality of why your provider is prescribing it

While both types of drugs aim to deliver a therapeutic benefit, their regulatory pathways and manufacturing scales are fundamentally different

However, the FDA has issued warnings about safety risks

Call your insurance provider to ask what documentation they require, then work with your doctor to submit a prior authorization with supporting records like lab work, chart notes and evidence of prior lifestyle changes