Fda To Add Warning About Rare Heart Inflammation To Moderna Pfizer

As it did with Leqembi, the FDA will require Kisunla to include a warning for MRI-visible injuries called amyloid-related imaging abnormalities, or ARIA, which can include brain swelling and tiny

Pfizer is finally closing on approval of its rare disease therapy tafamidis in the US, several years after it first reached the market in Europe The FDA has accepted two separate marketing applic

a staggering 95% of rare diseases still lack FDA-approved treatments Rare disease clinical research programs are already disadvantaged by small populations, geographic diversity, and young

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The Food and Drug Administration approved a new Alzheimer's treatment called donanemab on Tuesday, clearing the way for the third addition to a new class of drugs aimed at slowing the brain's

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US FDA adds warning about rare heart inflammation to Pfizer, Moderna ...

The longer it takes for the US Food and Drug Administration (FDA) to make an approval decision, the longer it is before a drugmaker can begin making money to recover the cost of its investment

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