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If results are weak into the remodelling phase and starting dose was sub-3.2 mg, a dose increase and protocol modification may be warranted

Some meta-analysis of clinical trials concluded that remdesivir has shown in little to no mortality benefit, but probably improves the clinical output and decreases serious adverse events of hospitalized patients with COVID-19

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The factors that affect the risk for anaphylactic-type reactions to iron dextran products are not fully known but limited clinical data suggest the risk may be increased among patients with a history of drug allergy or multiple drug allergies

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