CV, For Pharmacists, Doctor of pharmacy
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Usama Rehman has experience as both a university lecturer in pharmacology and a pharmacist. As a lecturer, he helped over 300 students each semester understand topics through classroom discussions. As a pharmacist, he assisted customers in chronic disease management and advised them on proper medication usage. Rehman also worked as an industrial pharmacist where he improved a company's customer service rating by 27% through attention to detail. He holds degrees from the University of Lahore and Harvard Medical School.
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Mr. Chithran Augustin has over 3 years of experience as a pharmacist in Abu Dhabi. He currently works as an in-charge pharmacist at Al Ahliya Grand Pharmacy, where he is responsible for dispensing and compounding drugs, patient counseling, insurance processing, and ensuring compliance with HAAD guidelines. Prior to this role, he worked as a clinical research coordinator at Christian Medical College & Hospital in India, where he conducted clinical trials and ensured protocols were followed according to ICH and GCP guidelines. He holds a Master's Degree in Pharmacy from The Tamil Nadu Dr. MGR Medical University and is a licensed pharmacist in both India and Abu Dhabi.
Sajid kp pharmacist cv updated
When you review my enclosed resume you will find that I possess over 5 years of Pharmacy experience in busy retail and clinical environments, with an active HAAD license in the state of Abu Dhabi, UAE. Throughout my career I have held positions as an Pharmacist Trainee, Pharmacist and Pharmacy in Charge. I am currently working with Standard Pharmacy attached to Unique care well Medical Center,Musaffah, Abu Dhabi as a Pharmacist in Charge since July 2014. Some of my job responsibilities include counseling the patients, supervising and mentoring pharmacy staff to provide excellent customer service and handling purchase.
PMS and Outsourcing - Copy.pptx
Post-marketing surveillance involves monitoring drug safety after market release. It identifies rare or long-term adverse effects not seen in clinical trials. Manufacturers must report serious adverse events to regulatory agencies. Outsourcing bioavailability and bioequivalence studies to contract research organizations allows companies to access expertise and resources while reducing costs and time to market. CROs conduct clinical trials, data analysis, and reporting according to Good Clinical Practice standards. Qualification of appropriate CROs involves assessing capabilities, infrastructure, compliance history, and collaboration effectiveness.
Systematic approach in answering medicine information queries.pptx
This document outlines an 8-step systematic approach for answering medicine information queries. The steps include: 1) securing requester details, 2) obtaining background information, 3) refining and categorizing the question, 4) developing a search strategy using literature hierarchy, 5) interpreting data from multiple references, 6) formulating a timely response with references, 7) conducting follow-up and documenting outcomes, and 8) maintaining quality assurance through updated references and procedures. The nature of queries may involve efficacy, dosing, adverse reactions, interactions, and use in special populations. A comprehensive literature search is conducted systematically through textbooks, databases, and primary sources.
Hospital pharmacy
Hospital pharmacy involves the procurement, storage, compounding, and distribution of drugs to patients by qualified pharmacists. The goals of hospital pharmacy are to provide qualified pharmacists to patients and health care facilities, assist in providing an adequate supply of pharmacists, and promote research. Objectives include educating staff on drugs, ensuring availability of medications at reasonable cost, and establishing drug information services. Key functions are pharmacy activities like dispensing and preparing injectable drugs, maintaining records, and educating nurses and patients. A hospital pharmacy requires adequate space, equipment, and personnel like pharmacists to fulfill its roles.
Therapeutic Drug Monitoring
Therapeutic drug monitoring (TDM) involves measuring drug concentrations in patients' blood to optimize drug therapy. TDM is useful for drugs with a narrow therapeutic index, high inter-individual variability, or when the relationship between concentration and clinical effects is well established. The TDM process includes requesting the test with relevant clinical information, collecting a proper blood sample, measuring drug levels in the laboratory, interpreting the results clinically, and adjusting drug dosing regimen accordingly to maintain concentrations within the therapeutic range. TDM aims to maximize drug effectiveness while minimizing toxicity.
Pharmacy Industrial Report By Praveen Singh B.phrma final year
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B.Pharma final year students
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1.Brooks, Baddi, Himachal Pradesh
2. Helios-II Baddi, Himachal Pradesh
Fresher resume
Denny Mathew is a pharmacist seeking opportunities with strong qualifications in pharmacology and pharmaceutical technology. He has over 1 year of work experience as a counselor for MSD processes at HCL Technologies in Hyderabad. He holds an M.Pharmacy degree in pharmacology from JNTU Kakinada with a CGPA of 6.75 and conducted research on the antidiabetic activity of Rhus Mysorensis for his thesis project. He is skilled in Microsoft Office, motivated, hard-working, and has excellent problem-solving and communication abilities.
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pharmacist resume (1)
Mr. Chithran Augustin has over 3 years of experience as a pharmacist in Abu Dhabi. He currently works as an in-charge pharmacist at Al Ahliya Grand Pharmacy, where he is responsible for dispensing and compounding drugs, patient counseling, insurance processing, and ensuring compliance with HAAD guidelines. Prior to this role, he worked as a clinical research coordinator at Christian Medical College & Hospital in India, where he conducted clinical trials and ensured protocols were followed according to ICH and GCP guidelines. He holds a Master's Degree in Pharmacy from The Tamil Nadu Dr. MGR Medical University and is a licensed pharmacist in both India and Abu Dhabi.
Sajid kp pharmacist cv updated
When you review my enclosed resume you will find that I possess over 5 years of Pharmacy experience in busy retail and clinical environments, with an active HAAD license in the state of Abu Dhabi, UAE. Throughout my career I have held positions as an Pharmacist Trainee, Pharmacist and Pharmacy in Charge. I am currently working with Standard Pharmacy attached to Unique care well Medical Center,Musaffah, Abu Dhabi as a Pharmacist in Charge since July 2014. Some of my job responsibilities include counseling the patients, supervising and mentoring pharmacy staff to provide excellent customer service and handling purchase.
PMS and Outsourcing - Copy.pptx
Post-marketing surveillance involves monitoring drug safety after market release. It identifies rare or long-term adverse effects not seen in clinical trials. Manufacturers must report serious adverse events to regulatory agencies. Outsourcing bioavailability and bioequivalence studies to contract research organizations allows companies to access expertise and resources while reducing costs and time to market. CROs conduct clinical trials, data analysis, and reporting according to Good Clinical Practice standards. Qualification of appropriate CROs involves assessing capabilities, infrastructure, compliance history, and collaboration effectiveness.
Systematic approach in answering medicine information queries.pptx
This document outlines an 8-step systematic approach for answering medicine information queries. The steps include: 1) securing requester details, 2) obtaining background information, 3) refining and categorizing the question, 4) developing a search strategy using literature hierarchy, 5) interpreting data from multiple references, 6) formulating a timely response with references, 7) conducting follow-up and documenting outcomes, and 8) maintaining quality assurance through updated references and procedures. The nature of queries may involve efficacy, dosing, adverse reactions, interactions, and use in special populations. A comprehensive literature search is conducted systematically through textbooks, databases, and primary sources.
Hospital pharmacy
Hospital pharmacy involves the procurement, storage, compounding, and distribution of drugs to patients by qualified pharmacists. The goals of hospital pharmacy are to provide qualified pharmacists to patients and health care facilities, assist in providing an adequate supply of pharmacists, and promote research. Objectives include educating staff on drugs, ensuring availability of medications at reasonable cost, and establishing drug information services. Key functions are pharmacy activities like dispensing and preparing injectable drugs, maintaining records, and educating nurses and patients. A hospital pharmacy requires adequate space, equipment, and personnel like pharmacists to fulfill its roles.
Therapeutic Drug Monitoring
Therapeutic drug monitoring (TDM) involves measuring drug concentrations in patients' blood to optimize drug therapy. TDM is useful for drugs with a narrow therapeutic index, high inter-individual variability, or when the relationship between concentration and clinical effects is well established. The TDM process includes requesting the test with relevant clinical information, collecting a proper blood sample, measuring drug levels in the laboratory, interpreting the results clinically, and adjusting drug dosing regimen accordingly to maintain concentrations within the therapeutic range. TDM aims to maximize drug effectiveness while minimizing toxicity.
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Fresher resume
Denny Mathew is a pharmacist seeking opportunities with strong qualifications in pharmacology and pharmaceutical technology. He has over 1 year of work experience as a counselor for MSD processes at HCL Technologies in Hyderabad. He holds an M.Pharmacy degree in pharmacology from JNTU Kakinada with a CGPA of 6.75 and conducted research on the antidiabetic activity of Rhus Mysorensis for his thesis project. He is skilled in Microsoft Office, motivated, hard-working, and has excellent problem-solving and communication abilities.
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Dr. Balwant Salunke has over 15 years of experience in clinical research, regulatory affairs, and academics. He holds a Ph.D. in Pharmacology and has worked in various roles such as Manager of Regulatory Affairs, Senior Executive, and Lecturer. His expertise includes bioequivalence studies, clinical trials, ANDA submissions to US FDA, and regulatory writing. He has published 5 research papers as the first author and reviewed several international manuscripts.
Genetic polymorphism in drug transport
This document discusses genetic polymorphisms in drug transport proteins and how they can impact drug pharmacokinetics and toxicity. It introduces two major superfamilies of transport proteins - ATP-binding cassette (ABC) transporters and solute carrier (SLC) proteins. Specific ABC transporters discussed include P-glycoprotein (ABCB1), the multidrug resistance proteins ABCC1 and ABCG2. The document also summarizes key SLC transporters and provides examples of important substrates for each. Genetic variations in these transport proteins can significantly influence individual responses to drugs like irinotecan used in cancer chemotherapy.
Medication history interview
This document outlines the process and importance of taking a thorough medication history. It discusses that medication history identifies allergies and past medication use, and is the starting point for medication reconciliation and review. The goals are to obtain complete information on all prescription and nonprescription medications, perceived benefits or side effects, and allergies. This helps identify potential medication problems and develop a care plan to improve outcomes. The document then describes how to collect both subjective and objective patient data, from various sources like interviews, records, and providers. It provides a script of questions to ask patients and tips for thorough history taking. The steps of patient selection, preparation, conducting the interview privately, documenting, and following up are also outlined.
Drug distribution system in a hospital.pptx
Drug distribution system in a hospital
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Automated Dispensing Machines in Pharmacies
Maher Ishak is the owner and manager of Woodbury Pharmacy in Highland Mills, New York. Maher Ishak introduced automation to Woodbury Pharmacy in 2006 with the Scrip Pro Robot dispensing system, thus freeing the staff to concentrate on the needs of customers.
Protocol for tdm
This document outlines a protocol for conducting a therapeutic drug monitoring study, including sections for the title, investigators, study location, patient recruitment details, need for the study, objectives, patient selection criteria, procedures for blood sample collection and storage, instruments for measuring drug and clinical levels, report preparation, clinical interpretation, and conclusion.
2. Hospital Pharmacy and its Organisation.pptx
Hospital pharmacy and its organization
Definition, functions of hospital pharmacy, Organization structure, Location, Layout and staff requirements, and Responsibilities and
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Drug development process
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Choose a molecule to target with a drug
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Test the target and confirm its role in the disease
Drug Discovery
Find a promising molecule (a “lead compound”)
that could become a drug
Introduction to clinical pharmacokinetics
The document discusses various concepts in pharmacokinetics including absorption, distribution, metabolism, and excretion of drugs in the body over time. It explains key mechanisms of absorption such as passive diffusion and carrier-mediated transport. Distribution of drugs in tissues is described using the volume of distribution concept. Metabolism and excretion of drugs via different routes is also summarized. The relationship between pharmacokinetics and pharmacodynamics is explained using drug concentration-time curves. Clinical applications of pharmacokinetic principles including therapeutic drug monitoring and dosage adjustment are also highlighted.
Documentation clinical trial
Clinical trials are research studies performed in humans to test new drugs or treatments. They follow a multi-phase process to test safety and efficacy. The document defines clinical trials and describes their purpose to discover or verify clinical and pharmacological effects of investigational products. It also outlines the different types of clinical trials including treatment, prevention, and screening trials. The phases of clinical trials are explained including phases I-III. Key documents for clinical trials are also listed such as the investigator's brochure, clinical study protocol, case report forms, informed consent forms, and clinical study reports.
IN VIVO AND SCALE-UP PROCESS APPROVAL CHANGES.pptx
The document discusses in vivo and scale-up process approval changes. It defines in vivo as experiments done on living organisms. SUPAC guidelines provide regulatory guidance for scale-up batches and post-approval changes. Changes are categorized as minor, major, or moderate. Level 1 changes have minimal impact while Level 3 changes likely impact quality. Requirements include chemistry documentation, dissolution testing, and bioequivalence studies depending on the level of change. Site, batch size, equipment, and process changes are also discussed along with associated testing requirements.
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A medication history interview involves collecting detailed information about all medications a patient is currently taking or has taken in the past. This provides insights into allergies, adherence to treatment, and use of alternative medicines. The goals are to identify discrepancies in medication records and gather additional information to inform care. Key information collected includes current and past medications, OTC drugs, reactions, adherence, and sources like pharmacies. Through counseling, patients can better understand their treatment and improve medication management to enhance outcomes.
Drug Therapy Monitoring
Introduction to daily activities of clinical pharmacist.
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That slides would help students to know about clinical trials, safety of patient/healthy subjects and about data management.
General Introduction on therapeutic drug monitoring
Concept of narrow therapeutics drugs, understanding therapeutic drug monitoring definitions, indications
Therapeutic drug monitoring
This document provides an overview of therapeutic drug monitoring (TDM). It defines TDM as the measurement of drug concentrations in blood or plasma to guide dosage adjustments for effective and safe treatment. The goals of TDM are to ensure maximal therapeutic benefit and minimal toxicity by achieving appropriate drug concentrations at the site of action. Several factors can cause variability in individual drug response, including pharmacokinetic factors like absorption and clearance, as well as pharmacodynamic factors like genetic polymorphisms and drug interactions. TDM is indicated for drugs with a narrow therapeutic index, a lack of clinical endpoints, or significant inter-individual variability. It involves collecting samples at standardized times, measuring drug levels, and interpreting the results with clinical context to optimize individual patient dos
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This document discusses the detection and monitoring of adverse drug reactions (ADRs). It outlines that ADRs are detected through pre-marketing studies such as acute toxicity and specific animal tests as well as clinical trials. Post-marketing surveillance also plays an important role in ADR detection through spontaneous reporting systems and epidemiological methods. In hospitals, healthcare professionals can detect ADRs by closely monitoring high-risk patients and collecting detailed patient data to assess causality and severity of suspected ADRs.
INDIVIDUAL PRESCRIPTION METHOD
This document discusses individual prescription methods used in small hospitals. It defines an individual prescription as one written for a specific patient after a medical assessment. Individual prescription methods involve the hospital pharmacy dispensing medications directly to patients based on their prescriptions. This system requires low manpower and allows for close control of inventory and interactions between medical staff. However, it may increase costs and be difficult without a pharmacist present. The document outlines standards for writing valid individual prescriptions, including prescriber and patient information, dates, and refill procedures.
Drug Regulatory Affairs- 2
1) Regulatory affairs professionals play important roles in coordinating scientific efforts with regulatory needs throughout a product's lifecycle. They help companies reduce time to market and maximize resources.
2) Key responsibilities include evaluating marketing applications, issuing approvals, developing guidelines, inspecting sites, and monitoring drug safety.
3) In the pharmaceutical industry, regulatory affairs professionals develop regulatory strategies, prepare applications, maintain relationships with health authorities, and ensure compliance.
Pharmacogenetics
This document discusses personalized medicine and pharmacogenetics. It explains that individuals respond differently to drugs due to genetic variations, so studying pharmacogenetics is important for selecting the right drug and dose for each patient. Many examples are provided of genetic polymorphisms that influence drug metabolism and effects. The implications of teratogenic drugs on fetal development are also reviewed, noting the most vulnerable period of organogenesis. The goal of personalized medicine is outlined as providing the right drug, dose, indication and time of treatment for each individual patient based on their genetic profile.
2015_ashp_mcm_slides_final.pdf
This document discusses trends in pharmacy education and considerations for new faculty members pursuing an academic career. It notes that the majority of pharmacy faculty are on calendar year, full-time appointments and that pharmacy practice faculty now comprise over 50% of pharmacy school faculty. The document outlines expectations for teaching, research/scholarship, patient care, and service depending on tenure versus non-tenure track positions. It emphasizes showing evidence of one's accomplishments in these areas for promotion through activities like publishing, presenting, securing grants, and developing new educational programs.
Final_Presentation_Resume.p174006
Catherine Newkirk has over 18 years of experience in pharmacy management and operations in both retail and clinical settings. She has owned and operated Medicap Pharmacy and has held pharmacy manager positions at CVS Pharmacies and North Carolina Central University Student Health Services. She has expertise in areas such as pharmacy management, business operations, team building and training, medication compounding, and quality assurance. She maintains active licensure as a pharmacist in North Carolina.
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Dr. Balwant Salunke has over 15 years of experience in clinical research, regulatory affairs, and academics. He holds a Ph.D. in Pharmacology and has worked in various roles such as Manager of Regulatory Affairs, Senior Executive, and Lecturer. His expertise includes bioequivalence studies, clinical trials, ANDA submissions to US FDA, and regulatory writing. He has published 5 research papers as the first author and reviewed several international manuscripts.
Genetic polymorphism in drug transport
This document discusses genetic polymorphisms in drug transport proteins and how they can impact drug pharmacokinetics and toxicity. It introduces two major superfamilies of transport proteins - ATP-binding cassette (ABC) transporters and solute carrier (SLC) proteins. Specific ABC transporters discussed include P-glycoprotein (ABCB1), the multidrug resistance proteins ABCC1 and ABCG2. The document also summarizes key SLC transporters and provides examples of important substrates for each. Genetic variations in these transport proteins can significantly influence individual responses to drugs like irinotecan used in cancer chemotherapy.
Medication history interview
This document outlines the process and importance of taking a thorough medication history. It discusses that medication history identifies allergies and past medication use, and is the starting point for medication reconciliation and review. The goals are to obtain complete information on all prescription and nonprescription medications, perceived benefits or side effects, and allergies. This helps identify potential medication problems and develop a care plan to improve outcomes. The document then describes how to collect both subjective and objective patient data, from various sources like interviews, records, and providers. It provides a script of questions to ask patients and tips for thorough history taking. The steps of patient selection, preparation, conducting the interview privately, documenting, and following up are also outlined.
Drug distribution system in a hospital.pptx
Drug distribution system in a hospital
Dispensing of drugs to inpatients, types of drug distribution systems, charging policy and labelling, Dispensing of drugs to ambulatory patients, and Dispensing of controlled drugs.
Automated Dispensing Machines in Pharmacies
Maher Ishak is the owner and manager of Woodbury Pharmacy in Highland Mills, New York. Maher Ishak introduced automation to Woodbury Pharmacy in 2006 with the Scrip Pro Robot dispensing system, thus freeing the staff to concentrate on the needs of customers.
Protocol for tdm
This document outlines a protocol for conducting a therapeutic drug monitoring study, including sections for the title, investigators, study location, patient recruitment details, need for the study, objectives, patient selection criteria, procedures for blood sample collection and storage, instruments for measuring drug and clinical levels, report preparation, clinical interpretation, and conclusion.
2. Hospital Pharmacy and its Organisation.pptx
Hospital pharmacy and its organization
Definition, functions of hospital pharmacy, Organization structure, Location, Layout and staff requirements, and Responsibilities and
functions of hospital pharmacists.
Drug development process
Pre-discovery
Understand the disease
Target Identification
Choose a molecule to target with a drug
Target Validation
Test the target and confirm its role in the disease
Drug Discovery
Find a promising molecule (a “lead compound”)
that could become a drug
Introduction to clinical pharmacokinetics
The document discusses various concepts in pharmacokinetics including absorption, distribution, metabolism, and excretion of drugs in the body over time. It explains key mechanisms of absorption such as passive diffusion and carrier-mediated transport. Distribution of drugs in tissues is described using the volume of distribution concept. Metabolism and excretion of drugs via different routes is also summarized. The relationship between pharmacokinetics and pharmacodynamics is explained using drug concentration-time curves. Clinical applications of pharmacokinetic principles including therapeutic drug monitoring and dosage adjustment are also highlighted.
Documentation clinical trial
Clinical trials are research studies performed in humans to test new drugs or treatments. They follow a multi-phase process to test safety and efficacy. The document defines clinical trials and describes their purpose to discover or verify clinical and pharmacological effects of investigational products. It also outlines the different types of clinical trials including treatment, prevention, and screening trials. The phases of clinical trials are explained including phases I-III. Key documents for clinical trials are also listed such as the investigator's brochure, clinical study protocol, case report forms, informed consent forms, and clinical study reports.
IN VIVO AND SCALE-UP PROCESS APPROVAL CHANGES.pptx
The document discusses in vivo and scale-up process approval changes. It defines in vivo as experiments done on living organisms. SUPAC guidelines provide regulatory guidance for scale-up batches and post-approval changes. Changes are categorized as minor, major, or moderate. Level 1 changes have minimal impact while Level 3 changes likely impact quality. Requirements include chemistry documentation, dissolution testing, and bioequivalence studies depending on the level of change. Site, batch size, equipment, and process changes are also discussed along with associated testing requirements.
Medication history interview
A medication history interview involves collecting detailed information about all medications a patient is currently taking or has taken in the past. This provides insights into allergies, adherence to treatment, and use of alternative medicines. The goals are to identify discrepancies in medication records and gather additional information to inform care. Key information collected includes current and past medications, OTC drugs, reactions, adherence, and sources like pharmacies. Through counseling, patients can better understand their treatment and improve medication management to enhance outcomes.
Drug Therapy Monitoring
Introduction to daily activities of clinical pharmacist.
Drug therapy monitoring,
Medication chart review
Clinical Progress
Pharmacist intervention
Detection and management of ADRs
Clinical Trial Safety Monitoring.pptx
That slides would help students to know about clinical trials, safety of patient/healthy subjects and about data management.
General Introduction on therapeutic drug monitoring
Concept of narrow therapeutics drugs, understanding therapeutic drug monitoring definitions, indications
Therapeutic drug monitoring
This document provides an overview of therapeutic drug monitoring (TDM). It defines TDM as the measurement of drug concentrations in blood or plasma to guide dosage adjustments for effective and safe treatment. The goals of TDM are to ensure maximal therapeutic benefit and minimal toxicity by achieving appropriate drug concentrations at the site of action. Several factors can cause variability in individual drug response, including pharmacokinetic factors like absorption and clearance, as well as pharmacodynamic factors like genetic polymorphisms and drug interactions. TDM is indicated for drugs with a narrow therapeutic index, a lack of clinical endpoints, or significant inter-individual variability. It involves collecting samples at standardized times, measuring drug levels, and interpreting the results with clinical context to optimize individual patient dos
Detection and monitoring of ADRs
This document discusses the detection and monitoring of adverse drug reactions (ADRs). It outlines that ADRs are detected through pre-marketing studies such as acute toxicity and specific animal tests as well as clinical trials. Post-marketing surveillance also plays an important role in ADR detection through spontaneous reporting systems and epidemiological methods. In hospitals, healthcare professionals can detect ADRs by closely monitoring high-risk patients and collecting detailed patient data to assess causality and severity of suspected ADRs.
INDIVIDUAL PRESCRIPTION METHOD
This document discusses individual prescription methods used in small hospitals. It defines an individual prescription as one written for a specific patient after a medical assessment. Individual prescription methods involve the hospital pharmacy dispensing medications directly to patients based on their prescriptions. This system requires low manpower and allows for close control of inventory and interactions between medical staff. However, it may increase costs and be difficult without a pharmacist present. The document outlines standards for writing valid individual prescriptions, including prescriber and patient information, dates, and refill procedures.
Drug Regulatory Affairs- 2
1) Regulatory affairs professionals play important roles in coordinating scientific efforts with regulatory needs throughout a product's lifecycle. They help companies reduce time to market and maximize resources.
2) Key responsibilities include evaluating marketing applications, issuing approvals, developing guidelines, inspecting sites, and monitoring drug safety.
3) In the pharmaceutical industry, regulatory affairs professionals develop regulatory strategies, prepare applications, maintain relationships with health authorities, and ensure compliance.
Pharmacogenetics
This document discusses personalized medicine and pharmacogenetics. It explains that individuals respond differently to drugs due to genetic variations, so studying pharmacogenetics is important for selecting the right drug and dose for each patient. Many examples are provided of genetic polymorphisms that influence drug metabolism and effects. The implications of teratogenic drugs on fetal development are also reviewed, noting the most vulnerable period of organogenesis. The goal of personalized medicine is outlined as providing the right drug, dose, indication and time of treatment for each individual patient based on their genetic profile.
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The document discusses the extended and expanded roles of nurses. It outlines various nursing roles such as health promoter, counselor, teacher, advocate, and manager. Extended roles involve tasks traditionally done by doctors that nurses can perform after additional training. Expanded roles enlarge the nursing scope to better meet patient needs. The conclusion states that technological and health changes require nurses to adapt and be prepared to handle various responsibilities.
CV2pdf
Bob Jochums is a pharmacist with over 20 years of experience at Walgreens and as a primary care resident at the VA Medical Center in Atlanta. He holds a Doctor of Pharmacy degree from Mercer University Southern School of Pharmacy, where he graduated magna cum laude. He is licensed as a pharmacist in Georgia and certified in immunization and CPR/AED.
Patient Education.pptx
Nurses’ patient education is important for building patients’ knowledge, understanding and preparedness for self-management. The ultimate goal of patient educational program is to achieve long-lasting changes in behavior by providing patients with the knowledge to allow them to make autonomous decisions to take ownership of their care as much as possible and improve their own outcomes.
CONCEPT OF PATIENT EDUCATION
Education on health issues is necessary for a patient’s physical and mental health.
Everybody finds themselves in situations where they require special knowledge and skills in order to meet their basic needs and sustain their lives.
All patients have the right to be educated on maintaining their health, disease prevention, and health promotion.
Health promotion is the process of advancing knowledge, influencing attitudes, and determining relevant solutions so that people can make informed choices, change their behavior and subsequently attain a desirable level of physical and mental health improve their social and physical environment.
Effective patient education starts from the time patients are admitted to the hospital and continuous until they are discharged. Nurses should take advantage of any appropriate opportunity throughout a patient’s stay to teach the patient about self-care.
The self- care instruction may include teaching patients how to inject insulin, bathe an infant or change a colostomy pouching system.
MEANING OF PATIENT EDUCATIONThe Latin origin of the word doctor “decree” means “to teach" and the education of patients and their families, as well as communities, is the responsibility of all physicians.
Family physicians are uniquely suited to take a leadership role in patient education.
Family physicians build long- term, trusting relationships with patients, providing opportunities to encourage and reinforce changes in health behavior.
Patient education enables patients to assume better responsibility for their own health care, improving patients’ ability to manage acute and chronic disorders.
Patient education provides opportunities to choose healthier lifestyles and practice preventive medicine.
Patient education attracts patients to the provider and increases patients’ satisfaction with their care, while at the same time decreasing the provider’s risk of liability.
Patient education promotes patient-centered care and as a result, patients’ active involvement in their plan of care.
Patient education increases adherence to medication and treatment regimens, leading to a more efficient and cost- effective health care delivery system
Patient education ensures continuity of care and reduces the complications related to illness and incidence of disorder/disease.
Patient education maximizes the individual’s independence with home exercise programs and activities that promote independence in activities of daily living as well as continuity of care needed
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CV, For Pharmacists, Doctor of pharmacy
- 1. UNIVERSITY LECTURER IN PHARMACOLOGY AT UOL: • Helped students understand topics by initiating and moderating classroom discussions. • Delivered high-quality instruction to more than 300 students every semester. AS A PHARMACIST AT UOL TEACHING HOSPITAL: • Assisted customers with chronic disease management. • Advised customers on medication usage and efficacy, promoting correct dosages to maintain health. INDUSTRIAL PHARMACIST AT HILTON PHARMA: • Maintained excellent standards of service through impeccable attention to detail. • Improved company customer service rating by 27%. PUNJAB GROUP OF COLLEGES: • FSC, PRE-MEDICIAL, 2010 UNIVERSITY OF LAHORE: • DOCTOR OF PHARMACY ,2015 HARVARD MEDICIAL SCHOOL: • MASTER IN CLINICAL SERVICE OPERATIONS. USAMA REHMAN P H A R M A C I S T GET IN CONTACT: USAMA REHMAN PERSONAL PROFILE Professional Skills: CAREER INTEREST: WORK EXPERIENCE EDUCATION HISTORY Home: 053 - 7516601 Mobile: 0320 -6836837 House# 14/35,Main Bazar Lalamusa, Gujrat usama.rehman60@gmail.com usama.rehman60@yahoo.com Seeking a challenging carrer within a dynamic and progressive organisation where enthusiasm, dedication and the ability to manage tasks effectively are pre requisite in driving the organisation forward. • Dispensing and managing hospital pharmacy • Study of rational use of drugs • Promoting Pharmaceutical care approaches in community • Selecting/Quantification of Drug Requirement etc • Promotion of Rational Drug Use in society. • Research in drug use behaviours/patterns. • Pharmaceutical care practice in hospital pharmacies. • Community health development projects.