Medical side effects tracking

A system for monitoring medical events for adverse effects comprising:

• at least one processor configured to:
• identify one or more medical events within medical information of a patient by applying first analytics to the medical information, wherein the medical information includes unstructured information;
• determine potential adverse effects of the identified medical events and corresponding time intervals of occurrence by applying second analytics to medical reference information, wherein effect information includes the identified medical events, determined potential adverse effects, and corresponding time intervals of occurrence;
• determine from the effect information one or more adverse effects for a medical event of the patient and the corresponding time intervals of occurrence, wherein determining the one or more adverse effects includes:
• generating a confidence score for each of the determined potential adverse effects:
• determining the one or more adverse effects from the determined potential adverse effects based on the confidence score for the determined potential adverse effects satisfying a threshold;
• and
• generating a timeline of the determined one or more adverse effects, wherein the timeline indicates the corresponding time intervals of occurrence for each of the determined one or more adverse effects and time intervals between each of the determined one or more adverse effects and the medical event of the patient;
• and
• notify a user of the determined one or more adverse effects prior to initiation of the corresponding time intervals of occurrence based on alignment of conditions of the patient with the timeline.

A computer program product for monitoring medical events for adverse effects comprising:

• one or more computer readable storage media collectively having program instructions embodied therewith, the program instructions executable by a processor to cause the processor to:
• identify one or more medical events within medical information of a patient by applying first analytics to the medical information, wherein the medical information includes unstructured information;
• determine potential adverse effects of the identified medical events and corresponding time intervals of occurrence by applying second analytics to medical reference information, wherein effect information includes the identified medical events, determined potential adverse effects, and corresponding time intervals of occurrence;
• determine from the effect information one or more adverse effects for a medical event of the patient and the corresponding time intervals of occurrence, wherein determining the one or more adverse effects includes:
• generating a confidence score for each of the determined potential adverse effects;
• determining the one or more adverse effects from the determined potential adverse effects based on the confidence score for the determined potential adverse effects satisfying a threshold;
• and
• generating a timeline of the determined one or more adverse effects, wherein the timeline indicates the corresponding time intervals of occurrence for each of the determined one or more adverse effects and time intervals between each of the determined one or more adverse effects and the medical event of the patient;
• and
• notify a user of the determined one or more adverse effects prior to initiation of the corresponding time intervals of occurrence based on alignment of conditions of the patient with the timeline.