Shared Health Record - Logical model of Emergency Health Record.

Information about the patient's blood group.

Record of the patient's blood group according to the AB0 system (A, B, AB, 0).

Record of Rh(D) factor.

Code identifying the type of blood group test performed.

Date and time when the result was determined.

Record of allergy or other significant adverse reaction to a substance or medicinal product.

Identification of the substance, medicinal product, or other substance causing the reaction.

Type of allergen in terms of origin.

Substance, group of substances, or environmental factor to which the patient is allergic or hypersensitive. The causative agent can be expressed using a substance code, ATC group, or SÚKL product code (in the case of medicinal products).

Information on whether it is an allergy or intolerance.

Clinical manifestations of the reaction.

Clinical severity of manifestation.

Date when the allergy/reaction was first diagnosed (onset).

Healthcare provider who recorded the data.

Other data includes records of significant adverse events. These typically include adverse drug reactions, transfusion reactions, complications during the administration of blood products, etc.

Classification of the event (e.g., adverse drug reaction, transfusion reaction).

A substance, drug, or other factor suspected of causing the event.

Date and time when the adverse event occurred.

Healthcare provider who recorded the data.

Medicinal products used in the patient during the provision of healthcare services by inpatient care providers over the last 12 months.

Code of the medicinal product administered to the patient during hospitalization.

The quantity of the medicinal product administered.

The date and time when the medicinal product was administered to the patient in an inpatient facility.

The provider who recorded the data – inpatient facility.

Shared Health Record - Logical model of Emergency Health Record.

Information about the patient's blood group.

Record of the patient's blood group according to the AB0 system (A, B, AB, 0).

Record of Rh(D) factor.

Code identifying the type of blood group test performed.

Date and time when the result was determined.

Record of allergy or other significant adverse reaction to a substance or medicinal product.

Identification of the substance, medicinal product, or other substance causing the reaction.

Type of allergen in terms of origin.

Substance, group of substances, or environmental factor to which the patient is allergic or hypersensitive. The causative agent can be expressed using a substance code, ATC group, or SÚKL product code (in the case of medicinal products).

Information on whether it is an allergy or intolerance.

Clinical manifestations of the reaction.

Clinical severity of manifestation.

Date when the allergy/reaction was first diagnosed (onset).

Healthcare provider who recorded the data.

Other data includes records of significant adverse events. These typically include adverse drug reactions, transfusion reactions, complications during the administration of blood products, etc.

Classification of the event (e.g., adverse drug reaction, transfusion reaction).

A substance, drug, or other factor suspected of causing the event.

Date and time when the adverse event occurred.

Healthcare provider who recorded the data.

Medicinal products used in the patient during the provision of healthcare services by inpatient care providers over the last 12 months.

Code of the medicinal product administered to the patient during hospitalization.

The quantity of the medicinal product administered.

The date and time when the medicinal product was administered to the patient in an inpatient facility.

The provider who recorded the data – inpatient facility.

Shared Health Record - Logical model of Emergency Health Record.

Information about the patient's blood group.

Record of the patient's blood group according to the AB0 system (A, B, AB, 0).

Record of Rh(D) factor.

Code identifying the type of blood group test performed.

Date and time when the result was determined.

Record of allergy or other significant adverse reaction to a substance or medicinal product.

Identification of the substance, medicinal product, or other substance causing the reaction.

Type of allergen in terms of origin.

Substance, group of substances, or environmental factor to which the patient is allergic or hypersensitive. The causative agent can be expressed using a substance code, ATC group, or SÚKL product code (in the case of medicinal products).

Information on whether it is an allergy or intolerance.

Clinical manifestations of the reaction.

Clinical severity of manifestation.

Date when the allergy/reaction was first diagnosed (onset).

Healthcare provider who recorded the data.

Other data includes records of significant adverse events. These typically include adverse drug reactions, transfusion reactions, complications during the administration of blood products, etc.

Classification of the event (e.g., adverse drug reaction, transfusion reaction).

A substance, drug, or other factor suspected of causing the event.

Date and time when the adverse event occurred.

Healthcare provider who recorded the data.

Medicinal products used in the patient during the provision of healthcare services by inpatient care providers over the last 12 months.

Code of the medicinal product administered to the patient during hospitalization.

The quantity of the medicinal product administered.

The date and time when the medicinal product was administered to the patient in an inpatient facility.

The provider who recorded the data – inpatient facility.