DRUG AND MEDICAL DEVICE SAFETY AND SUPPORT INFORMATION REPORTING SYSTEM, PROCESSING DEVICE AND METHOD

• US 20110145018A1
• Filed: 02/17/2011
• Published: 06/16/2011
• Est. Priority Date: 03/21/2005
• Status: Abandoned Application

• Current Assignee: PDR Network LLC (PSKW LLC)
• Original Assignee: PDR Network LLC (PSKW LLC)
• Inventors: Prakash, Era, Fotsch, Edward J., Guidice, Debra Del
• Application Number:
  US13/029,770
• Publication Number:
  US 20110145018A1
• Time in Patent Office: Days
• US Class Current: 705/3
• CPC Class Codes: G06Q 10/10 Office automation; Time management
• CPC Class Codes: G06Q 50/20 Education
• CPC Class Codes: G06Q 50/26 Government or public services business processes related to the transportation industry G06Q50/40
• CPC Class Codes: G16H 10/60 for patient-specific data, e.g. for electronic patient records
• CPC Class Codes: G16H 15/00 ICT specially adapted for medical reports, e.g. generation or transmission thereof
• CPC Class Codes: G16H 70/40 relating to drugs, e.g. their side effects or intended usage

Abstract

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.

Claims

1. A reporting system to provide drug or medical device information to a healthcare provider, the system comprising:

a first processing device including a first processor to execute first machine readable instructions stored on a first storage device, the first processing device to provide first drug or medical device information for a first drug or first medical device in response to the execution of the first machine readable instructions;

a second processing device including a second processor to execute second machine readable instructions stored on a second storage device, the second processing device to provide second drug or medical device information for the first drug or first medical device in response to the execution of the second machine readable instructions;

a third processing device including a third processor to execute third machine readable instructions stored on a third storage device, the third processing device to receive and map the first and second drug or medical device information into compiled drug or medical device information in response to the execution of the first machine readable instructions; and

a fourth processing device including a fourth processor to execute fourth machine readable instructions stored on a fourth storage device, the fourth processing device to provide an electronic health record of a patient to a healthcare provider in response to the execution of the fourth machine readable instructions, the electronic health record including an indication of the compiled drug or medical device information;

wherein the third processing device provides the compiled drug or medical device information to the healthcare provider in response to a selection of the indication of the compiled drug information during a workflow of the healthcare provider.

2. The system of claim 1, wherein the first drug information is drug information in electronic form and provided by the FDA and wherein the second drug information is in electronic form and provided by a manufacturer of the drug.

3. The system of claim 1, wherein the first drug information includes at least one of a drug product label, a drug safety communication, a medication guide, REMS information and FDA early warnings.

4. The system of claim 3, wherein the second drug information includes at least one of a drug product label and an alert regarding the drug.

5. The system of claim 1, wherein the compiled drug information includes summaries of the first and second drug information provided by the third processing device.

6. The system of claim 5, wherein the indication of the compiled drug information includes a hyperlink in the electronic health record of the patient.

7. The system of claim 1, wherein the electronic health record includes an indication to report adverse events associated with the drug, and wherein the third processing device receives information regarding adverse events associated with the drug, and wherein the third processing device aggregates and transfers the information regarding adverse events to the first and second processing device.

8. The system of claim 7, wherein the first and second processing devices update the first and second drug information in response to the information regarding adverse events associated with the drug.

9. The system of claim 7, further comprising:

a fifth processing device including a fifth processor to execute fifth machine readable instructions stored on a fifth storage device, the fifth processing device to receive information regarding adverse events associated with the drug in response to the execution of the fifth machine readable instructions, the fifth processing device to transfer information regarding clinical education or CMEs to the third processing device in response to the information regarding adverse events associated with the drug.

10. A method performed by a processing device to report drug or medical device information to a healthcare provider, the method comprising:

receiving, by the processing device, first drug or medical device information from a first source;

receiving, by the processing device, second drug or medical device information from a second source;

combining, by the processing device, the first drug or medical device information and second drug or medical device information into compiled drug or medical device information;

providing, by the processing device, the compiled drug or medical device information in response to a selection by a healthcare provider during a workflow of the healthcare provider;

receiving, by the processing device, information regarding an adverse event regarding the drug or medical device; and

aggregating, by the processing device, information regarding the adverse event of the drug or medical device with other information regarding an adverse event of the drug or medical device into an adverse event report; and

transferring, by the processing device, the adverse report to the first and second source so that the first and second drug or medical device information is updated.

11. The method of claim 10, wherein the first source includes a processing device have a storage device to store FDA information, and wherein the first drug information includes at least one of a drug product label, a drug safety communication, a medication guide, REMS information and FDA early warnings.

12. The method of claim 11, wherein the second source includes a processing device having a storage device to store drug manufacturer information, and wherein the second drug information includes at least one of a product label and an alert regarding the drug.

13. The method of claim 10, further comprising providing, by the processing device, information regarding drug or medical device information that is selected from at least one of samples of the drug or medical device, coupons of the drug or medical device, financial assistance for a patient prescribed the drug or to use the medical device, patient education regarding the drug or medical device, clinical reference for the drug or medical device, access to ask the expert, physician communications/education, patient communications/education, registries, clinical trials and patient medication and adherence programs.

14. The method of claim 10, further comprising:

transferring, by the processing device, the adverse report to a processing device having a storage device to store insurance information; and

receiving, from the processing device having insurance information, information regarding clinical education or CMEs in response to the adverse report.

15. The method of claim 14, further comprising:

transferring, by the processing device, the adverse report to a processing device having a storage device to store information to provide an electronic health record; and

receiving, from the processing device having electronic health record information, information regarding education or training for the drug or medical device which is accessible by the healthcare provider.

16. The method of claim 15, wherein the selection by a healthcare provider includes the healthcare provider selecting a hyperlink associated with the drug or medical device at an electronic health record of a patient.

17. A processing device to report drug or medical device safety information to a healthcare provider, the processing device comprising:

at least one storage device to store a plurality of different types of safety information regarding a plurality of drugs or medical devices;

at least one processor, coupled to the storage device;

the at least one storage device to store executable machine readable instructions for controlling the processor; and

the at least one processor is operative with the executable machine readable instructions to;

receive the plurality of different types of safety information regarding the plurality of drugs or medical devices from multiple sources;

associate the plurality of different types of safety information for a respective drug or medical device in the plurality of drugs or medical devices with a respective plurality of internal identifiers;

receive a selection of a drug or medical device by the healthcare provider during a workflow; and

provide at least one of the plurality of different types of safety information for the selected drug or medical device to the healthcare provider by using an identifier in the plurality of internal identifiers.

18. The processing device of claim 17, wherein the at least one processor is operative with the executable machine readable instructions to further:

receive information regarding a plurality of adverse events of using the drug or medical device;

aggregate the plurality of adverse events to provide a report; and

transfer the report to at least one of the sources so that at least of one the plurality of different types of safety information that is received is updated with current safety information.

19. The processing device of claim 18, wherein the plurality of different types of safety information are in a plurality of different types of formats.

20. The processing device of claim 19, wherein the plurality of different types of safety information includes at least one of following types of safety information:

full label, concise, alert, FDA DHCPLs, MGs, REMS-term summary, REMS-Notification Summary and FDA Early Warning.

21. The processing device of claim 17, wherein the at least one processor is operative with the executable machine readable instructions to:

associate external identifiers corresponding to respective drug or medical device in the plurality of drugs or medical devices with the respective plurality of internal identifiers.