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FDA Adverse Events Reporting System Report Source 2018

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FAERS (FDA Adverse Event Reporting System) is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products. It is a useful tool for FDA (U.S....

FDA Adverse Events Reporting System Patient Outcome 2018

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FAERS (FDA Adverse Event Reporting System) is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products. It is a useful tool for FDA (U.S....

FDA Adverse Events Reporting System Drug Therapy Dates 2018

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FAERS (FDA Adverse Event Reporting System) is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products. It is a useful tool for FDA (U.S....

FDA Adverse Events Reporting System Drug Reaction 2018

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FAERS (FDA Adverse Event Reporting System) is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products. It is a useful tool for FDA (U.S....

FDA Adverse Events Reporting System Drug Indication 2018

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FAERS (FDA Adverse Event Reporting System) is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products. It is a useful tool for FDA (U.S....

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FDA Adverse Events Reporting System Report Source 2018

FDA Adverse Events Reporting System Patient Outcome 2018

FDA Adverse Events Reporting System Drug Therapy Dates 2018

FDA Adverse Events Reporting System Drug Reaction 2018

FDA Adverse Events Reporting System Drug Indication 2018