Fachapotheker/in FPH Spital study plan
Fachapotheker/in FPH Spital · Give each week a clear focus.
8 weeks · About 7 hours per week
Clinical pharmacy and pharmaceutical care in hospitalized patients (medication reconciliation, drug therapy review, ward rounds) & Pharmacotherapy of major disease states and internal medicine (infectious diseases, cardiology, oncology, intensive care, pediatrics, geriatrics)
List the core steps of medication reconciliation at admission, transfer, and discharge, and explain how each step reduces unintended discrepancies.
Compare the mechanisms, monitoring parameters, and key adverse effects of the main antibiotic classes used in hospital practice (beta-lactams, glycopeptides, aminoglycosides, fluoroquinolones).
Outline the components of a structured drug therapy review (indication, effectiveness, safety, adherence) and apply them to two common internal medicine scenarios (e.g., heart failure, COPD exacerbation).
Identify high-risk medications in hospitalized patients and describe at least three specific safety checks for each.
Your checkpoint
A one-page medication reconciliation checklist and a 10-item drug therapy review template, each with brief rationale, ready for use on the ward.
Pharmacotherapy of major disease states and internal medicine (infectious diseases, cardiology, oncology, intensive care, pediatrics, geriatrics) & Clinical pharmacology, pharmacokinetics and therapeutic drug monitoring
Explain the pathophysiology and first-line pharmacotherapy of acute coronary syndrome, heart failure, and atrial fibrillation, including dosing and monitoring in renal impairment.
Describe the principles of antimicrobial stewardship and apply them to choose empiric therapy for common infections (pneumonia, urinary tract infection, sepsis) based on local resistance patterns.
Calculate creatinine clearance using Cockcroft-Gault and adjust doses of at least five renally eliminated drugs accordingly.
Interpret therapeutic drug monitoring results for vancomycin and aminoglycosides, and recommend dose adjustments based on pharmacokinetic principles.
Your checkpoint
A set of 10 dose-adjustment flashcards for renally eliminated drugs, each showing the calculation and the recommended adjustment, plus a one-page TDM interpretation guide.
Pharmacotherapy of major disease states and internal medicine (infectious diseases, cardiology, oncology, intensive care, pediatrics, geriatrics) & Medication safety, pharmacovigilance and risk management (ADRs, medication errors, hygiene, cytotoxic safety)
Summarize the mechanisms, monitoring, and management of immune-related adverse events for checkpoint inhibitors and of febrile neutropenia in oncology patients.
Describe the pharmacokinetic changes in critically ill patients (altered volume of distribution, augmented renal clearance) and adjust dosing of sedatives and antibiotics accordingly.
Explain age-related pharmacokinetic and pharmacodynamic changes and apply them to deprescribing decisions in geriatric patients (e.g., benzodiazepines, anticholinergics).
Classify medication errors by stage (prescribing, dispensing, administration) and propose one preventive strategy for each stage.
Your checkpoint
A two-page summary table of high-alert medications in oncology and intensive care, listing monitoring parameters and error-prevention strategies.
Drug compounding, sterile and non-sterile preparations, hospital manufacturing and quality assurance (GMP, pharmacopoeia) & Hospital drug logistics and supply chain (procurement, storage, distribution, automated dispensing, narcotics handling)
Outline the key requirements of GMP for hospital manufacturing, including cleanroom classification, environmental monitoring, and validation of sterile processes.
Describe the principles of non-sterile compounding (weighing, mixing, quality control) and the documentation required for a magistral preparation.
Explain the procurement process for hospital drugs, including tender procedures, safety stock calculation, and management of drug shortages.
Compare storage requirements for different drug classes (cold chain, narcotics, hazardous drugs) and describe the associated documentation and security measures.
Your checkpoint
A process map for sterile compounding from prescription to release, annotated with critical control points and GMP references.
Hospital pharmacy organization, law and professional ethics (incl. Swissmedic, HMG, BetmVV, hospital formulary governance) & Hospital drug logistics and supply chain (procurement, storage, distribution, automated dispensing, narcotics handling)
Summarize the Swiss legal framework for hospital pharmacy practice: HMG, BetmVV, Swissmedic requirements for hospital exemptions, and narcotics regulations.
Explain the governance of a hospital formulary, including the role of the pharmacy and therapeutics committee and the criteria for drug inclusion.
Describe the design and operation of automated dispensing systems and their impact on medication safety and inventory control.
Outline the legal and practical requirements for handling narcotics in the hospital, from prescribing to destruction.
Your checkpoint
A one-page flowchart of the hospital formulary decision process, from request to committee decision to implementation, with legal references.
Medication safety, pharmacovigilance and risk management (ADRs, medication errors, hygiene, cytotoxic safety) & Clinical pharmacology, pharmacokinetics and therapeutic drug monitoring
Explain the pharmacovigilance system in Switzerland, including reporting requirements for ADRs to Swissmedic and the role of the hospital pharmacist.
Apply pharmacokinetic principles to interpret plasma concentration-time curves and recommend individualized dosing for a drug with narrow therapeutic index.
Describe hygiene measures for preventing healthcare-associated infections, including hand hygiene, isolation precautions, and cleaning of compounding areas.
Outline safe handling procedures for cytotoxic drugs at all stages (receipt, preparation, administration, waste) and the associated monitoring of occupational exposure.
Your checkpoint
A one-page ADR reporting checklist and a one-page cytotoxic safe-handling checklist, each with key steps and responsible roles.
Research, evidence-based medicine, statistics and scientific communication & Management, leadership, teaching and interprofessional collaboration
Critically appraise a randomized controlled trial using a standard checklist (e.g., CONSORT) and interpret the results in the context of clinical practice.
Explain basic statistical concepts (p-values, confidence intervals, number needed to treat) and apply them to interpret a published study.
Describe strategies for effective interprofessional collaboration on ward rounds and for teaching pharmacy students and junior staff.
Outline the principles of change management and leadership in a hospital pharmacy setting, including how to implement a quality improvement project.
Your checkpoint
A one-page critical appraisal of a recent clinical trial relevant to hospital pharmacy practice, including a summary of strengths, limitations, and applicability.
Hospital pharmacy organization, law and professional ethics (incl. Swissmedic, HMG, BetmVV, hospital formulary governance) & Clinical pharmacy and pharmaceutical care in hospitalized patients (medication reconciliation, drug therapy review, ward rounds) & Pharmacotherapy of major disease states and internal medicine (infectious diseases, cardiology, oncology, intensive care, pediatrics, geriatrics) & Drug compounding, sterile and non-sterile preparations, hospital manufacturing and quality assurance (GMP, pharmacopoeia) & Hospital drug logistics and supply chain (procurement, storage, distribution, automated dispensing, narcotics handling) & Medication safety, pharmacovigilance and risk management (ADRs, medication errors, hygiene, cytotoxic safety) & Clinical pharmacology, pharmacokinetics and therapeutic drug monitoring & Research, evidence-based medicine, statistics and scientific communication & Management, leadership, teaching and interprofessional collaboration
Review all domains using a self-assessment checklist and identify three areas of weakness for further study.
Complete a timed mock examination covering all domains and analyze incorrect answers to identify knowledge gaps.
Integrate learning from all domains by solving two complex case scenarios that require medication reconciliation, therapeutic drug monitoring, and legal considerations.
Create a personal continuing education plan for the next six months, targeting the identified weaknesses.
Your checkpoint
A completed self-assessment checklist with a prioritized list of three knowledge gaps and a six-month continuing education plan.
Milestones
Week 2: Can explain and apply medication reconciliation and drug therapy review in two clinical scenarios, and correctly adjust doses for renal impairment in five cases.
Week 4: Can describe GMP requirements for sterile compounding and the hospital drug procurement process, and has produced a process map with critical control points.
Week 6: Can explain pharmacovigilance reporting and cytotoxic safe handling, and interpret TDM results to recommend individualized dosing.
Week 8: Achieved at least 70% on the mock examination and completed a self-assessment with a continuing education plan.