A
reporting system, including a
processing device, and method provides
drug and
medical device safety and support information during a
workflow of a healthcare provider. The
system and method electronically acquires, maps, generates, compiles, verifies and transfers in real
time critical information regarding particular drugs and medical devices required by healthcare providers, such as a prescriber, at the optimum time in which the healthcare provider needs the information. In an embodiment, the
drug and
medical device safety information is accessed from an associated healthcare website, such as an Electronic Health
Record (EHR)
web site, during a prescription stage in the healthcare providers
workflow for a particular patient. The
system and method also includes an adverse
reporting system that allows for the
drug and
medical device safety information to be updated and accurately reported in an efficient and up to date manner. In an embodiment, a healthcare provider reports an adverse event or reaction to a drug by a patient during a
workflow at a EHR
web site. The adverse event information is forwarded to the Federal
Drug Administration (FDA) and the particular drug manufacturer which may update the corresponding drug information. The updated drug information may then be reported by the
system to insure that healthcare providers receive the most current, accurate and complete safety information during a workflow. In embodiments, the updated drug and
medical information may be provided to malpractice insurance carriers to further ensure safety.