Pharmaceutical emergency response plan example
In life, work and study, sometimes encounter unforeseen emergencies, in order to be able to make a timely emergency response to reduce the consequences of the accident, you have to need to formulate an emergency response plan in advance. Preparation of emergency plans need to pay attention to what problems? The following is a sample of emergency plan for drug emergencies that I have organized for you for your reference and reference, I hope to help friends in need.
Drug Emergency Emergency Response Plan 1
In order to ensure that emergencies can be dealt with quickly after the occurrence of emergencies, to ensure the quality of pharmacy services and the successful completion of medical rescue work, the specific this emergency drug supply and pharmacy management emergency response plan, please follow the implementation.
I. Early warning system for emergencies
1. Early warning system for emergencies refers to all kinds of accidental emergency medical rescue of all conditions, including infectious diseases, poisoning rescue, floods, earthquakes, fires and so on. The start of the early warning system: in the event of an emergency emergency, according to its nature, category and severity, start the emergency response. The director or deputy director and the person in charge of the pharmacy are immediately and directly notified by the staff on duty, who is responsible for coordinating the work, and the supervisors of all relevant departments are responsible for organizing and assisting. In accordance with the hospital's deployment, the resources of the whole department are utilized to assist in the completion of the rescue work. Infectious diseases category A, B in accordance with the county or the hospital plan in the three-level warning system of the standard start.
2, start the first level of emergency response: the director is responsible for coordinating the work, the replacement is to assist the director in charge of the work of the deputy director.
Start the second level of emergency response: to assist the director of the pharmacy department in charge of the work of the deputy director is responsible for coordinating the work.
Activate the third level of emergency response: the person in charge of the pharmacy is responsible for coordinating the work.
3, rescue emergency call: in case of rescue patients, the staff on duty should be ready to emergency drugs, proactive participation in rescue work. When there is a shortage of drugs, they should take the initiative to contact the pharmacy or other pharmacies to make up for it as soon as possible, and at the same time, they should use their professional knowledge to actively find substitutes to solve the problem.
Second, the organization
⒈, in the emergency hospital pharmacy management committee's main responsibilities include:
(1) the development and review of therapeutic and preventive medicine program: including first-line personnel, second-line personnel and other medical staff of the preventive medicine program and emergency treatment of emergency medicine program; and to develop appropriate Emergency emergency related medication catalog, and emergency emergency rescue medication catalog.
(2) review the dosage forms and quantities of emergency medicines, review the catalog of rescue medicines such as respiratory failure medicines, circulatory failure medicines, hepatic and renal insufficiency medicines, poisoning rescue, floods, fires, earthquakes, etc.;
(3) development and review of the program of drug safety monitoring;
pak Pharmacy Department to exercise the responsibilities of the Pharmacy Committee in emergencies and set up a Pharmacy Department Emergency Response Leadership Team, whose members include: the department director, deputy director, the head of each pharmacy, and the pharmacy staff.
5 professional functional groups were set up under the Pharmacy Section with the following functions:
(1) Human resources group: the director of the section is the leader, responsible for the integration of personnel in emergencies, stabilizing the mood of the staff, and life protection, etc. Other groups should report regularly to the director of the section on the situation of the personnel (including attendance, infection).
① personnel integration, including the re-setting of the staff of the groups, staff deployment, new groups of temporary positions, staff arrangements, scheduling, once the first level of emergency response state, should be announced that the whole section (group) suspension, all staff reserved 24-hour contact phone, and each person's duties, and made into a form.
② Stabilize the mood of the staff, staff incentives and should establish the appropriate constraints, and the appropriate application of psychological knowledge to appreciate the practical difficulties of staff.
③ Do a good job of protecting the necessary living goods, such as ensuring that the staff in the quarantine area, `food, living supplies to provide; work safety, such as the development of precautionary measures, disinfection, the implementation of isolation and so on.
④ Ensure the smooth communication channel with the superior leadership, affirm to the superior the work situation and special characteristics of the Pharmacy Department, and coordinate various temporary problems.
(2) drug security supply team: the designated pharmacy staff is also the head of the pharmacy team, and its main responsibilities are as follows:
(1) to obtain information on medicines from multiple channels, market information tracking; and according to the treatment guidelines formulated by the hospital or expert group to do the basic purchasing plan including treatment guidelines or expert group designated drugs in the drug list of medicines, write down the name of the drug, the duration of the course of treatment, the dosage, and the amount of money, The number of people who are expected to receive treatment, and the need to consider the substitutability between drug treatment programs. In the procurement process to ensure the supply of scarce drugs.
② Responsible for the purchase, storage and distribution of hospital drugs and disinfectants. The pharmacy is responsible for the delivery of drugs to the hospital area, but each time the drugs need to be delivered to the fever clinic or isolation ward of the semi-contaminated area, and the staff of the contaminated area to hand over.
③ Poisoning rescue, flood, earthquake, fire and other rescue medicines, may not be the hospital standing drugs, but it is important to know which pharmaceutical companies produce these drugs and their supply channels.
④ supply of stock medicines and coordinate the transfer of rescue medicines in each pharmacy.
(3) drug transfer group: the director of the pharmacy is responsible for, its main work is:
① daily hospital drug transfer work, the implementation of other temporary tasks related to the transfer.
② effective protection (taking into account the possibility of individual febrile patients to the clinic), the prescription should be transmitted by the hospital network system, the manual transmission of the prescription should be sterilized and properly stored to avoid cross-infection in the hospital.
③ The routine work of the fever clinic pharmacy includes: drug delivery, scheduling, account management and sterilization.
④ Provide clinical information on medication, ensure the supply of medication, reserve medication for the consultation program, prevent backlogs, and do patient-oriented medication counseling and publicity work.
⑷ clinical pharmacy group: by the deputy director of the concurrent or temporary appointment, is responsible for the emergency drug information, clinical pharmacy and drug safety aspects of the work.
① Timely collection and organization of drug information, in an appropriate manner to the clinical delivery of rational drug use information.
② ADR monitoring, report collection and reporting, feedback.
(5) Drug Quality Control Group: the director of the pharmacy is also responsible for the head of the group, whose work includes:
① Procurement of drugs, quality control of donated drugs.
② purchased, donated drugs, drug test report check.
③ Check the quality inspection report and expiration date of each batch of donated drugs.
Third, the emergency emergency management of the pharmaceutical matters
(1) in the event of an emergency response to the above emergency response to start after the pharmacy staff must be in accordance with the program to carry out the work in their respective positions. In addition to the above division of labor, each pharmacist should be proactive, flexible and flexible measures, the courage to participate in the rescue work.
(2) the emergency outbreak of infectious diseases after the pharmacy work of the aftermath
① for infectious disease patients to provide drug supply ward pharmacy should be set up in a clean area, due to special needs into the contaminated area, semi-contaminated area of the aftermath of the drugs should be dealt with in accordance with the following methods.
② drugs for the treatment of hospitalized patients with infectious diseases, should be placed in a clean area. Daily set of drugs to the whole package of drugs should not enter the contaminated area, semi-contaminated area. However, due to special needs into the contaminated area of the drugs, in the infectious disease is effectively controlled, the contaminated area is ready to remove, the remaining drugs should be contaminated area disinfection. Disinfection of remaining medicines in the contaminated area should be carried out after the final disinfection of the contaminated environment and houses. The method of disinfecting the remaining medicines is to soak them in 0.2%-0.5% peroxyacetic acid solution. Disinfected remaining medicines are regarded as medical waste, which can be put into double yellow garbage bags and disposed of in designated areas, and shall not be recycled for use. Contaminated areas of drugs before sterilization and destruction, should be registered in the books, the amount of statistics.
③ Into the semi-contaminated area of the treatment of drugs. Drugs should not enter the semi-polluted areas as far as possible. Special needs to enter the semi-contaminated area of the drugs, in the infectious disease is effectively controlled, semi-contaminated area is ready to withdraw, should be semi-contaminated area of the remaining drugs for disinfection. The disinfection of the remaining medicines entering the semi-contaminated area should be carried out after the final disinfection of the environment and the house, and the disinfection of the outer package or the original package of the medicines in the semi-contaminated area should be carried out by wiping with 0.2%-0.5% of peroxyacetic acid solution. Oral medicines whose original packaging has been opened shall not be recalled for use. The rest of the drugs can continue to be used after the disinfection of the outer and original packaging is wiped and approved by the Infection Office of the hospital. Semi-polluted area of the drug disinfection after the book registration, the amount of statistics.
④ Disposal of disinfected drugs after infectious diseases. The anti-infectious disease work needs to prepare sufficient disinfection drugs, and its disinfection drugs are mainly based on peroxyacetic acid and products containing effective chlorine. After the phase of anti-infectious disease work is over, other using units should be contacted first to reduce waste and avoid environmental pollution. After the expiration date of the disinfectant drugs, they shall not be sold.
⑤ Disposal of backlogged drugs. After the end of the phase of prevention and treatment of infectious diseases, in addition to ensuring the normal use of drugs within the validity period, such as the existence of a backlog of drugs, should be a timely and comprehensive statistics, backlog of drug information first to the supplier, and through timely feedback, in order to avoid blind stocking. The library to be dealt with backlog of drugs, after the inventory into the accounts to other units of use to contact or consult with the supplier to help contact the use. After the expiration of the expiration date shall not be used, and should be accounted for statistics, according to the relevant provisions of the destruction of reported losses.
(3) emergencies pharmaceutical management emergency plan also applies to other emergencies occurring pharmaceutical emergency management plan, according to the nature of environmental emergencies, categories and other different flexible response.
Pharmaceutical Emergency Response Plan 21 General
1.1 Purpose
For the effective prevention, timely control and disposal of safety emergencies arising from the application of the company's production and sales of medicines, to improve the company's rapid response and emergency response capabilities, to maximize the protection of people's safety of medicines, the development of this plan.
1.2 Preparation of the basis
"Chinese People's **** and the State Drug Administration Law", "Chinese People's **** and the State Drug Administration Law Enforcement Regulations", "Adverse Drug Reaction Reporting and Monitoring Measures"
1.3 Scope of application
This emergency plan applies to the application of the company to produce and sale of medicines for the safety of emergencies emergency response.
2 Leadership and related departments
2.1 Leadership
The establishment of the company's emergency leadership group
Leader: Wang Xinmin
Deputy Leader: Zheng Jun, Tang Weigang, Chen Shuhong
Members: Jia Zhenyu, Zhang Yanchun, Ma Pingfeng, Xu Xiaoyan, Wang Yanchun, Jiang Guiqin
2.2 Related departments
2.2 Responsibilities of the relevant departments
2.3 Scope of application
This emergency plan applies to the application of our production and sales of pharmaceuticals safety emergencies. Responsibilities
The Marketing Department is responsible for the production of safety emergencies when the batch of drugs sealed and retrieved, the Quality Assurance Department is responsible for the production of safety emergencies when the batch of drugs self-inspection and sent to the inspection, to the Shanxi Province and Xinzhou City, Drug Administration and the Shanxi Provincial Adverse Drug Reaction Monitoring Center report, is responsible for the occurrence of the incident when the batch of drug information collection, evaluation, summary, reporting, and with the food and drug supervision and management departments to complete the corresponding work at all levels. It is also responsible for collecting, evaluating, summarizing and reporting information on the batch of drugs in which the incident occurred, and cooperating with the food and drug supervision and management departments at all levels to complete the corresponding work. The production management department is responsible for the investigation of safety emergencies when the batch of drugs.
3 Early warning and prevention mechanism
For the application of our production and sales of drugs found in drug safety emergencies, the Quality Assurance Department should be timely to the Shanxi Province and Xinzhou City Food and Drug Administration, Shanxi Provincial Department of Health, as well as Shanxi Province, the Adverse Drug Reaction Monitoring Center report, shall not be concealed, late report, or authorize others to conceal, late report.
4 Emergency Response
4.1 Start of the plan
In the event of drug safety emergencies by the general manager of the company announced the start of the emergency plan.
4.2 Response Procedures
Due to the application of our production and sales of drugs found in drug safety emergencies should be immediately reported by the Quality Management Department to the Shanxi Provincial Food and Drug Administration, Shanxi Provincial Department of Health, Shanxi Province, Adverse Drug Reaction Monitoring Center, and at the same time, to the Xinzhou City, Xinzhou City, drug supervision and management and the Xinzhou City Bureau of Health report. The company shall issue a notice within 24 hours to suspend the sale of the batch of products sold in all markets, and report to the Shanxi Provincial and Xinzhou Food and Drug Administration, Shanxi Provincial Department of Health and Xinzhou Municipal Bureau of Health and Shanxi Adverse Drug Reaction Monitoring Center within 24 hours by summarizing the production and sale of the drug in the whole country. The report includes the time and place of the incident, the name of the drug, the performance of the adverse event, the number of adverse reactions and deaths. The medical and health institutions were notified to stop using the drug immediately and seal it in a unified manner. The company organized relevant personnel to immediately go to the scene to grasp the first-hand information of the incident. Verify the production batch number of the product, and take emergency control measures at the first time on the drugs that caused the safety emergencies.
4.3 End of emergency response
The emergency was effectively controlled and the end of emergency response was announced.
5 Emergency security
5.1 Communication security
After the start of the emergency mechanism, the contact person Chen Shuhong, to ensure that 24 hours to answer the phone, fax, to ensure smooth information.
5.2 Financial security
The financial department to prepare sufficient funds to deal with emergencies.
6 Post-disposal
6.1 Post-disposal
After investigation if the violation of the provisions of the Drug Administration Law, causing damage to the drug users, the company bears the responsibility for compensation in accordance with the law.
6.2 Summary assessment
The Quality Assurance Department is responsible for writing the investigation report, summarizing and evaluating the investigation, and making recommendations for improvement. The summary report is reported to the Shanxi Province and Xinzhou Food and Drug Administration.
7 By-laws
7.1 Reporting information content
① The occurrence, development, handling and other relevant circumstances;
② Drug instructions (imported drugs need to provide foreign instructions);
③ Quality inspection reports;
④ Whether in the monitoring period;
⑤ Registration, re-registration time;
⑤ Registration and re-registration time;
⑥ Drug production approvals, and the time for the registration and re-registration of drugs.
⑥ drug production approvals;
⑦ implementation standards;
⑧ domestic and international drug safety research, domestic and international adverse drug reactions, including literature reports;
⑨ typical cases to fill out the "Adverse Drug Reaction/Event Reporting Form";
⑩ reporters and contact phone numbers.
7.2 Update of the plan
The Quality Assurance Department is responsible for reviewing and adjusting this plan. When the laws and regulations on which this plan is based, the institutions and personnel involved change significantly, or when defects are found in the implementation, it is responsible for organizing timely revision.
7.3 Implementation or effective date of the plan
This plan shall come into force from the date of approval.
Emergency plan for drug emergencies3
In order to effectively do a good job in school drug health protection, effective prevention, timely control and correct disposal of school drug health emergencies, to protect the health and safety of students, according to the "Chinese People's Republic of China *** and the State Drug Administration Law", "Chinese People's Republic of China *** and the implementation of the Drug Administration Law Regulations",
"School Health Regulations" and other relevant laws and regulations requirements, the development of the School Health Regulations.
"School health work regulations" and other relevant laws and regulations, the development of this plan.
First, the guiding ideology
"scientific concept of development" as the guide, adhere to the "safety first, prevention-oriented" policy, and strive to minimize the harm of accidents, to maintain the safety and stability of education. The safety and stability of education, to ensure that the normal order of teaching and learning in the school.
Second, the scope of the emergency response plan
This plan applies to the use of the school infirmary (health care) medicine health emergencies.
Third, the school drug health emergency leading group and responsibilities
1, the school drug health emergency leading group Group Leader: Fu Qiang
Deputy Leader: Yang Hong Peng Youbin
Members: Xu Yuancai, Wang Yan, the class teacher.
2, the school drug health emergency response leading group responsibilities
(1) immediately stop the use of drugs, and at the first time to report to the district health, education and Food and Drug Administration and other departments;
(2) to understand the cause of the incident, the number of people, the drugs that caused the incident, the patient's symptoms and so on;
(3) immediately send the sick teachers and students to hospitals
(4) retain the drugs, equipment and the scene of the adverse drug reaction incident;
(5) actively cooperate with the health, Food and Drug Administration departments to investigate, and according to its requirements to truthfully provide relevant materials and samples;
(6) the implementation of the health department required to take other measures, and to deal with the aftermath of the incident, to maintain normal education and teaching order of the school;
(7) the implementation of the health department to take other measures, and to maintain normal education and teaching order of the school;
(8) the implementation of the health department to take the following measures Normal teaching and learning order;
(7) with the health department to analyze the causes of adverse drug reactions, summarize the lessons learned, put forward corrective suggestions, to prevent the recurrence of similar events.
Fourth, the emergency disposal process
1. Incident discovery
The class teacher found that students in the school after the use of medicines in the infirmary (health room) diarrhea, abdominal pain, vomiting and other symptoms of physical discomfort, should be immediately notified by phone to the school doctor or health teacher, and send the students to the infirmary or health room. School doctors or health teachers in the classroom teacher's cooperation, the number of students onset, the condition of the preliminary investigation to understand.
2. Incident report
(1) After investigation and understanding, the school nurse or health teacher preliminary suspicion for students in the school to use the infirmary (health room) of the drugs produced by the adverse drug reaction events, should immediately report by phone to the school in charge of the leadership and the principal, the school in charge of the leadership should immediately report by phone to the District Education Commission primary and secondary school health care and make a detailed record, and at the same time, the school infirmary (health room) immediately stop using drugs, and the school infirmary (health room). Health room) immediately stop using drugs, retain the drugs that cause adverse drug reactions.
(2) District primary and secondary school health care received a report, immediately reported to the District Education Committee, and immediately with the District Food and Drug Administration, District Health Bureau staff rushed to the school for emergency response and investigation.
3. Medical treatment
(1) the condition of mild students near the treatment; more serious students, transferred to the district health administrative department designated medical institutions for treatment. At the same time, medical institutions to do a good job of medical emergency preparedness.
(2) The school will inform the parents of the sick students, and notify the parents to visit the hospital to take care of the students.
4. On-site investigation
The school actively cooperate with the health, Food and Drug Administration and other departments, the symptoms and signs of the sick student case investigation, and other school use the school infirmary (health room) the same kind of medicine for students to investigate.
5. Sample testing
Schools actively cooperate with the health, Food and Drug Administration and other departments, the school infirmary (health room) of the remaining drug sampling.
6. Environmental improvement
Schools actively cooperate with the health, Food and Drug Administration and other departments, the school infirmary (health room) to carry out inspection of the health status of the drug and environmental hygiene improvement, to further strengthen the awareness of drug health and safety.
7. Public opinion guidance
Schools should respect and satisfy the right to information of teachers, students and parents, in accordance with the relevant procedures, through a variety of forms, proactive, timely and accurate notification of adverse drug reactions related information, positive publicity of the relevant departments and the school to take measures to avoid false public opinion to disrupt the hearing and affecting the normal order of teaching and learning in schools and social stability.
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