Abstract: A patient-portable medication event monitor is disclosed which is capable of detecting the dispensing of doses of a particular medication from the monitor, comparing the dispensing detected with information concerning the desired dosing regimen for the certain medication and displaying graphically to the patient at least one feedback indication of the patient's degree of compliance or deviation with the desired regimen.

Abstract: A patient-portable medication event monitor is disclosed which is capable of detecting the dispensing of doses of a particular medication from the monitor, comparing the dispensing detected with information concerning the desired dosing regimen for the certain medication and displaying graphically to the patient at least one feedback indication of the patient's degree of compliance or deviation with the desired regimen.

Abstract: A patient-portable medication event monitor is disclosed which is capable of detecting the dispensing of doses of a particular medication from the monitor, comparing the dispensing detected with information concerning the desired dosing regimen for the certain medication and displaying graphically to the patient at least one feedback indication of the patient's degree of compliance or deviation with the desired regimen.

Abstract: A patient-portable medication event monitor is disclosed which is capable of detecting the dispensing of doses of a particular medication from the monitor, comparing the dispensing detected with information concerning the desired dosing regimen for the certain medication and displaying graphically to the patient at least one feedback indication of the patient's degree of compliance or deviation with the desired regimen.

Abstract: A label which notes the manipulation of objects which it labels by generating an altered electrical signature is provided.

Abstract: The present invention relates to a method and system of medication monitoring which includes analyzing data on the clinical consequences of variable patient compliance with prescribed drug regimens, communicating to caregivers and/or patients the compliance-dependent probabilities of two clinically important transitions in health status: substantive improvement in the patient's health status and substantive deterioration in the patient's health status, defining acceptable levels of the respective probabilities of deterioration and of improvement, and intervening when appropriate to improve the patient's compliance, in order to achieve mutually-agreed upon maintenance, improvement, or avoidance of deterioration in health status.

Abstract: The present invention relates to a system and method for managing a patient treatment program including a prescribed dosing regimen. The system and method develops and/or makes use of a pharmacokinetic model and a pharmacodynamic model and the monitored adherence of the patient to determine if and when testing should be performed. The system and method further determines if the prescribed dosing regimen should be adjusted, based upon a comparison of the results of the one or more tests and the results predicted by the one or more models.

Abstract: The system of portal-mediated, website-based analysis of medication dosing data provides a system for recording dosing history, analyzing the dosing history data, and providing a physician with the analysis of the dosing history data, as well as advice as to the steps to take to improve the patient's compliance or to prevent its further deterioration. The system for portal-mediated, website-based analysis of medication dosing includes a package, dispenser, or organizer adapted to provide a patient with medication, and to generate dosing history data, a webserver accessible through a website and adapted to receive said dosing history data through said website via the Internet, and a processor for analyzing the received dosing history data to thereby generate analysis data.

Abstract: The present invention relates to a method and system of medication monitoring which includes analyzing data on the clinical consequences of variable patient compliance with prescribed drug regimens, communicating to caregivers and/or patients the compliance-dependent probabilities of two clinically important transitions in health status: substantive improvement in the patient's health status and substantive deterioration in the patient's health status, defining acceptable levels of the respective probabilities of deterioration and of improvement, and intervening when appropriate to improve the patient's compliance, in order to achieve mutually-agreed upon maintenance, improvement, or avoidance of deterioration in health status.