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Adverse Effects and Reporting Adverse events or suspected contamination issues should be reported immediately to the manufacturer (Hospira/Pfizer) and relevant regulatory authorities (FDA MedWatch, poison control, or institutional pharmacovigilance systems)

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This condition is known as telogen effluvium

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Our selections are rigorously evaluated for safety, consistency, and efficacy during Phase III clinical trials

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I recognize that, but we're clear on what California's law is

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