See below: The fda's adverse events reporting system (aers) is for healthcare professionals (doctors, nurses) & consumers (you) to report any problems with meds to the fda after it has been released. Info: http://www.Fda.Gov/drugs/guidancecomplianceregulatoryinformation/surveillance/adversedrugeffects/default.Htm submit: https://www.Accessdata.Fda.Gov/scripts/medwatch/medwatch-online.Htm.
Answered 8/18/2013
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A doctor has provided 1 answer
A doctor has provided 1 answer
A doctor has provided 1 answer
A doctor has provided 1 answer
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