Pharmacy gave the wrong medicine, how to deal with problems compensation

Hospital pharmacy wrong medicine should be based on the actual loss to compensate. If the patient because of the wrong medication reasonable, necessary, and the consequences of the damage has a direct correlation with the relevant costs are required by the hospital to bear the responsibility of compensation. If there is no loss, no compensation.

A, the law stipulates that the hospital pharmacy to take the wrong medicine how to compensate?

The hospital pharmacy wrong medicine should be based on the actual loss to compensation.

1, the pharmacy to the patient to take the wrong medicine, if the patient or pharmacy staff found in time, timely replacement can be. If the two sides are found in time, and the patient unfortunately took the wrong drugs. Then from the objective situation, the pharmacy staff should bear the main fault, the patient should bear part of the fault of not checking. According to the pharmacy should bear the proportion of fault, and then multiplied by the damage caused by the fault of the loss, that is, the pharmacy should bear the amount of compensation.

2, the pharmacy as a compensation obligation, for the patient due to the error of medication produced by the reasonable, necessary, and the consequences of damage to the existence of correlation, medical expenses, lost wages, nursing care, accommodation costs, transportation costs, hospital meals and other costs, should be borne. However, the costs should be borne in accordance with the proportion of the responsibility of the pharmacy for the fault to be multiplied by the final amount of the amount of the actual amount of compensation payable by the pharmacy.

Two, engaged in pharmaceutical business activities need to comply with the provisions of what?

Engaged in pharmaceutical wholesale activities, should be approved by the local people's government of the provinces, autonomous regions and municipalities directly under the Central People's Government of the drug supervision and management department, to obtain a license to operate drugs. Engaged in pharmaceutical retail activities, should be approved by the local people's government at or above the county level drug supervision and management department, to obtain a drug license. No drug license, shall not operate drugs.

Drug license should be marked with the validity and scope of business, the expiration of the re-examination of the license.

Drug supervision and management departments to implement the drug license, in addition to the conditions set out, but also should follow the principle of facilitating the public to buy drugs.

Engaged in pharmaceutical business activities should have the following conditions:

(a) a pharmacist or other pharmacy technicians certified in accordance with the law;

(b) with the management of pharmaceutical products appropriate business premises, equipment, storage facilities and sanitation environment;

(c) with the management of pharmaceutical products appropriate quality management organization or personnel;

(d) to ensure the quality of drugs (D) to ensure the quality of drugs, regulations and systems, and in line with the State Council drug supervision and management department in accordance with the requirements of this law to develop quality management standards for drug business.

Engaged in pharmaceutical business activities, should comply with the drug business quality management standards, establish and improve the drug business quality management system to ensure that the whole process of drug business continues to meet the statutory requirements.

The state encourages and guides the retail chain operation of drugs. Engaged in drug retail chain business activities of the headquarters of the enterprise, should establish a unified quality management system, the retail enterprises under the management of the business activities to fulfill the responsibility.

The legal representative of the drug business enterprises, the main person in charge of the enterprise's overall responsibility for the drug business activities.

The state of the implementation of prescription drugs and non-prescription drugs classification and management system. Specific measures are formulated by the State Council drug supervision and management department in conjunction with the State Council department in charge of health.

The holder of the listed drug license, drug manufacturers, drug companies and medical institutions should be from the holder of the listed drug license or drug production, business qualification of enterprises to purchase drugs; however, the purchase of Chinese herbal medicine is not implemented except for the approval of management.

Drug business enterprises to purchase drugs, should establish and implement the purchase inspection and acceptance system, inspection of drug certificates and other identification; does not meet the prescribed requirements, shall not be purchased and sold.

Drug business enterprises purchase and sale of drugs, there should be true and complete purchase and sale records. Purchase and sale records should indicate the generic name of the drug, dosage form, specifications, product lot number, expiration date, marketing license holder, manufacturer, purchase and sale of units, purchase and sale of quantities, purchase and sale of prices, purchase and sale of the date and the State Council drug supervision and management department of the other content.

The medical institutions in the relevant diagnostic and treatment activities, must be careful. Because the staff of medical institutions and patients have contact with each other, the behavior will be engaged in a direct impact on patients. For example, the staff of the medical institution to take the wrong medication accidentally, resulting in the loss of the patient's wrong medication, it is necessary to compensate.