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According to the FDA-approved prescribing information, injection site reactions occurred in 1.4% of Ozempic patients versus 0.6% in placebo groups
As treatment continues and things are stable, the frequency may be reduced (for example, checks every 6 months)
FDA approval and launch: Once approved, the generic manufacturer can launch immediately unless there's an ongoing patent dispute
Your final dosage and personalized treatment plan will be determined during your consultation with a licensed healthcare provider
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