7 results about "Dose schedule" patented technology

Exemplary embodiments relate to automated medicament delivery (AMD) devices. Such devices may measure the level of an analyte and deliver medicament with the intent of maintaining the analyte at a target level or in a target range. The described methods and apparatuses apply a model to evaluate an effect of proposed future medicament doses on predicted analyte levels. The proposed future medicament doses and predicted analyte levels may be supplied to a cost function to select which of the proposed future medicament dose schedules results in optimal control of the predicted analyte levels. The cost function may apply a weighting scheme that weighs predictions in the near- and / or medium-term future more than longer-term predictions.

The present disclosure provides a patient system and method for interfacing with and controlling an oral medication dispensing device. The system registers the dispensing device to a particular patient and records biometric data regarding the patient. Upon verifying a dose schedule and biometric authentication of the patient, the system authorizes use of the medication dispensing device and causes an activator mechanism to activate. In doing so, an activator mechanism within the dispensing device moves a medication cartridge between a stored position and a dispensing position, where it can be compressed to safely and efficiently dispense medication to the patient.

The present invention relates to a drug administration schedule for HER2 inhibitors useful in the prevention and / or treatment of cancer, particularly to their dosage and administration in second-line or subsequent lines.

Accumulated path length for ions that reach a particular area of a patient is used in dose planning as an indicator of plan robustness. Also, the magnitude of the variations of the accumulated path lengths is determined for a number of beam directions, allowing beam directions to be selected for maximum robustness in treatment planning.

The present disclosure provides a physician system and method for interfacing with and controlling an oral medication dispensing device. The system registers a patient under the care of a doctor and records a dose schedule for the patient. The dose schedule specifies a particular medication and associated volume and timing interval for administration to the patient via a medication dispensing device. A medication cartridge is with the dose schedule. An invitation link is sent to the patient for the patient to link the physician system with their patient system and the medication dispensing device. The dose schedule can be pushed to the patient system to populate the patient system with the specifics of the dose schedule.

A non-transitory computer-readable storage medium is provided that includes instructions that, when executed by a computer, cause the computer to: execute a program for managing a medical condition or treatment of a user; monitoring a current administration schedule set within the program; determining whether the predetermined dose expires; determining an experience level of the user; in response to determining that the predetermined dose expires, generating a first notification alerting the user of the predetermined dose; and in response to detecting a user interaction with the first notification, providing a user interface that displays content related to the predetermined dose. At least a portion of the displayed content is based on an experience level of the user.

The invention discloses a clinical test drug dose progressive increase system, which comprises a system management end, a dose plan management module and a subject file management module, the monitoring and evaluation end comprises a dose detection module, a safety evaluation module and a warning module; the warning module is used for receiving the safety coefficient and comparing the safety coefficient with a preset standard coefficient, and if the safety coefficient exceeds a preset standard coefficient threshold value, alarm information is output. The analysis and communication end comprises a feedback suggestion module, a data analysis report generation module and a communication reminding function module; the feedback suggestion module is in signal connection with the dose detection module; the data analysis report generation module is in signal connection with the safety evaluation module and generates an analysis report strategy table; the communication reminding function module is in signal connection with the mobile terminal and is configured to receive the analysis report strategy table and send the analysis report strategy table to the mobile terminal. The application has the effects of improving the safety of closely monitoring the patient and carrying out necessary adjustment and intervention according to the monitoring result.