Albania Pharmacist Certification Exam (Provimi i Certifikimit) study materials
Albania Pharmacist Certification Exam (Provimi i Certifikimit) study resources

Albania Pharmacist Certification Exam (Provimi i Certifikimit) cheat sheet

Albania Pharmacist Certification Exam (Provimi i Certifikimit) · Keep the key ideas within reach.

Quick reference

Pharmaceutical Chemistry and Medicinal Chemistry

  • Henderson–Hasselbalch: pH = pKa + log([base]/[acid]); for a weak acid, percent ionized = 100/(1 + 10^(pKa − pH)).

  • Lipinski's rule of five: MW ≤ 500, logP ≤ 5, H-bond donors ≤ 5, H-bond acceptors ≤ 10; violation of two or more predicts poor oral bioavailability.

  • Bioisosteres: replace −OH with −NH2 or −CH3, or a carboxyl with a tetrazole, to preserve activity while altering metabolism or pKa.

  • Prodrugs are inactive derivatives metabolized to the active drug, e.g., enalapril to enalaprilat, or ester prodrugs of carboxylic acids to improve absorption.

  • Racemic mixtures: enantiomers may differ in potency and toxicity (e.g., S-warfarin is more potent than R-warfarin; thalidomide enantiomers differ in teratogenicity).

  • Structure–activity relationships: chain length, ring substitution pattern, and stereochemistry at the chiral center are the most common determinants of receptor affinity.

  • β-Lactam antibiotics act by acylating penicillin-binding proteins; the strained β-lactam ring is essential, and β-lactamase cleavage destroys activity.

  • Phase I metabolism (oxidation, reduction, hydrolysis) introduces or exposes polar groups; Phase II (glucuronidation, sulfation, acetylation) conjugates them for excretion.

  • pKa governs ionization and thus absorption: an acidic drug is largely unionized and absorbable in the stomach, whereas a basic drug is more unionized in the small intestine.

Quick reference

Pharmaceutics and Pharmaceutical Technology

  • Bioavailability F = (AUCoral × DOSEiv)/(AUCiv × DOSEoral); it expresses the fraction of the dose reaching systemic circulation unchanged.

  • First-pass metabolism reduces oral bioavailability; routes avoiding it include sublingual, rectal (partly), transdermal, and parenteral.

  • Tablet compression stages: die filling, metering, compaction (viscoelastic deformation), and ejection; capping and lamination result from entrapped air or excessive elastic recovery.

  • Dissolution testing: USP Apparatus I (basket) and II (paddle) are standard; similarity factor f2 ≥ 50 indicates comparable dissolution profiles.

  • Suspensions require a suspending agent and controlled flocculation to prevent caking; Stokes' law shows sedimentation rate rises with particle diameter squared.

  • Sterile products: terminal sterilization by moist heat at 121 °C for 15 min (F0 ≥ 8 min); aseptic processing is used for heat-labile products.

  • Emulsions are stabilized by surfactants reducing interfacial tension; HLB 8–18 favors oil-in-water, HLB 3–6 favors water-in-oil.

  • Zero-order release delivers drug at a constant rate independent of concentration; first-order release rate is proportional to remaining concentration.

  • Osmotic pump (OROS) tablets release drug by osmotic pressure through a semipermeable membrane at a near zero-order rate.

Quick reference

Pharmacology and Pharmacotherapy

  • Receptor types: ligand-gated ion channels (fast, ms), G-protein-coupled receptors (seconds), kinase-linked receptors (minutes), and nuclear receptors (hours, gene transcription).

  • Agonists activate receptors; competitive antagonists shift the dose–response curve right without reducing Emax; non-competitive antagonists lower Emax.

  • Therapeutic index = TD50/ED50; a narrow index (e.g., digoxin, warfarin, lithium) requires therapeutic drug monitoring.

  • Pharmacokinetic equations: Vd = Dose/C0; CL = ke × Vd; t½ = 0.693/ke; steady state is reached in about 4–5 half-lives.

  • Loading dose = (Vd × target concentration)/bioavailability; maintenance dose = (CL × target concentration)/bioavailability.

  • ACE inhibitors cause cough and hyperkalemia and are contraindicated in pregnancy; ARBs are an alternative when cough occurs.

  • β-Blockers reduce heart rate and myocardial oxygen demand; cardioselective agents (e.g., metoprolol) are preferred in asthma.

  • Aminoglycosides are bactericidal, concentration-dependent, and nephro/ototoxic; they require dose adjustment in renal impairment.

  • Opioid overdose is reversed by naloxone, a competitive μ-opioid antagonist; benzodiazepine overdose by flumazenil.

Quick reference

Pharmacognosy and Phytotherapy

  • Alkaloids are nitrogen-containing basic plant compounds (e.g., morphine from Papaver somniferum, quinine from Cinchona, atropine from Atropa belladonna).

  • Cardiac glycosides (digoxin from Digitalis lanata) inhibit Na+/K+-ATPase; their aglycone (genin) determines activity and the sugar moiety affects solubility and kinetics.

  • Tannins are polyphenols that precipitate proteins; they are astringent and used topically for hemostasis and in wound healing.

  • Essential oils are volatile terpenoids obtained by steam distillation; they are stored in tightly closed containers away from light and heat.

  • St. John's wort (Hypericum perforatum) induces CYP3A4 and reduces concentrations of oral contraceptives, warfarin, and ciclosporin.

  • Ginkgo biloba may increase bleeding risk with anticoagulants; its standardized extract is quantified by flavonoid glycosides and terpene lactones.

  • Senna and cascara contain anthraquinone glycosides with laxative action; long-term use risks electrolyte loss and dependence.

  • Standardization expresses the content of a marker compound per unit (e.g., 'standardized to 4% hypericin'); it ensures batch-to-batch consistency.

Quick reference

Toxicology and Clinical Toxicology

  • Paracetamol overdose: N-acetylcysteine restores glutathione; the Rumack–Matthew nomogram guides treatment based on the 4-hour plasma concentration.

  • Organophosphate poisoning: acetylcholinesterase inhibition causes SLUDGE/ DUMBELS; treat with atropine plus pralidoxime before enzyme 'aging'.

  • Methanol and ethylene glycol poisoning: fomepizole (or ethanol) inhibits alcohol dehydrogenase; severe cases need hemodialysis.

  • Iron poisoning: deferoxamine chelates iron; activated charcoal does not bind iron or lithium effectively.

  • Salicylate toxicity causes mixed respiratory alkalosis and metabolic acidosis; urinary alkalinization with sodium bicarbonate enhances elimination.

  • Cyanide toxicity: hydroxocobalamin or sodium thiosulfate plus sodium nitrite; it blocks cytochrome oxidase and cellular respiration.

  • Digoxin toxicity: treat with digoxin-specific Fab antibody fragments; hypokalemia increases toxicity risk.

  • Poisoning management principles: ABC stabilization, decontamination only if within 1 hour (activated charcoal 1 g/kg), and antidote when indicated.

  • Lead poisoning: chelate with calcium disodium edetate or dimercaptosuccinic acid (succimer); blood lead level guides severity.

Quick reference

Pharmaceutical Care and Clinical Pharmacy

  • Pharmaceutical care is the responsible provision of drug therapy to achieve definite outcomes that improve a patient's quality of life.

  • Medication reconciliation compares the patient's pre-admission list with current orders at admission, transfer, and discharge to prevent discrepancies.

  • The SOAP note format: Subjective, Objective, Assessment, and Plan; each problem is documented separately with measurable endpoints.

  • Adverse drug reaction causality: the Naranjo algorithm scores temporal relationship, dechallenge, rechallenge, and alternative causes.

  • Therapeutic drug monitoring is indicated for narrow-index drugs (digoxin, lithium, phenytoin, vancomycin, aminoglycosides) and for suspected non-adherence.

  • Counselling on inhalers: shake the device, exhale fully, actuate while inhaling, hold breath 10 seconds, and rinse mouth after inhaled corticosteroids.

  • Anticoagulation counselling: warfarin requires INR monitoring and consistent vitamin K intake; DOACs require renal function checks.

  • Medication adherence can be assessed with the Morisky scale; pill counts and refill records are objective alternatives.

  • Pharmacist interventions should follow the pharmaceutical care process: assessment, care plan, follow-up, and documentation of outcomes.

Quick reference

Pharmacy Legislation, Ethics, and Professional Practice

  • Prescription requirements generally include prescriber identification, patient data, drug name, strength, dosage form, quantity, directions, and date/signature.

  • Narcotic and controlled substances require special prescription forms, limited quantities, and strict record-keeping with secure storage.

  • Pharmacists must maintain confidentiality of patient information and disclose it only with consent or legal requirement.

  • Good Distribution Practice requires temperature-controlled storage, validated transport, and traceability records for medicinal products.

  • Dispensing errors must be documented and reported through pharmacovigilance; adverse drug reactions are reported to the national regulatory authority.

  • Generic substitution is permitted only where legally authorized; the pharmacist must inform the patient and the prescriber when required.

  • The pharmacist's ethical duty includes competence maintenance through continuing education and avoidance of conflicts of interest.

  • Medicines must be stored according to label (e.g., 2–8 °C cold chain, below 25 °C ambient); expired stock is quarantined and destroyed per regulation.

Quick reference

Pharmacoeconomics and Pharmacy Management

  • Cost-minimization analysis compares alternatives with equivalent clinical outcomes and considers only cost differences.

  • Cost-effectiveness analysis reports cost per unit of clinical outcome (e.g., cost per life-year or per mmHg reduction); lower ICER is more favorable.

  • Incremental cost-effectiveness ratio: ICER = (CostA − CostB)/(EffectA − EffectB); interpret against a willingness-to-pay threshold.

  • Cost–benefit analysis expresses both costs and outcomes in monetary units, yielding a net benefit or benefit-to-cost ratio.

  • Cost–utility analysis uses quality-adjusted life years (QALYs), where QALY = life expectancy × utility (0–1).

  • Inventory management: economic order quantity balances ordering and holding costs; ABC analysis classifies stock by value and turnover.

  • Break-even point in units = fixed costs/(price per unit − variable cost per unit).

  • Budget variance = actual cost − budgeted cost; a positive variance indicates overspending.

  • Pharmacy revenue components include dispensing margin, OTC sales, and clinical services; gross margin = revenue − cost of goods sold.

Quick reference

Biochemistry, Physiology, and Pathology

  • Glycolysis yields 2 ATP and 2 NADH per glucose; the complete oxidation of glucose yields about 30–32 ATP.

  • The sodium–potassium ATPase pumps 3 Na+ out and 2 K+ in per ATP, maintaining resting membrane potential.

  • The Henderson–Hasselbalch equation applied to bicarbonate: pH = 6.1 + log([HCO3−]/(0.03 × PaCO2)); normal pH 7.35–7.45.

  • Insulin lowers blood glucose by promoting glucose uptake and glycogen synthesis; glucagon raises it via glycogenolysis and gluconeogenesis.

  • The nephron: glomerular filtration, proximal tubular reabsorption (~65% of Na+ and water), loop of Henle concentration, distal and collecting duct regulation by aldosterone and ADH.

  • Atherosclerosis involves endothelial injury, LDL oxidation, macrophage foam-cell formation, and plaque rupture causing thrombosis.

  • Type 2 diabetes arises from insulin resistance plus progressive β-cell failure; HbA1c reflects average glycemia over about 3 months.

  • Liver function tests: ALT and AST reflect hepatocellular injury, ALP and GGT reflect cholestasis, and albumin and INR reflect synthetic function.

  • The renin–angiotensin–aldosterone system raises blood pressure via vasoconstriction and sodium retention; ACE inhibitors and ARBs block it.

Quick reference

Microbiology and Hygiene

  • Gram-positive bacteria have a thick peptidoglycan layer and stain purple; Gram-negative bacteria have a thin layer plus an outer membrane and stain pink.

  • Bacterial growth phases: lag, exponential (log), stationary, and death; the exponential phase is targeted by most antibiotics.

  • Sterilization kills all microorganisms including spores; disinfection reduces pathogens on inanimate surfaces but may not kill spores.

  • Autoclaving at 121 °C, 15 psi for 15 min achieves sterility; dry heat at 160–180 °C is used for glassware and powders.

  • Hand hygiene is the single most effective measure to prevent healthcare-associated infection; alcohol-based rubs are preferred when hands are not visibly soiled.

  • Antibiotic resistance mechanisms include enzymatic inactivation (β-lactamases), efflux pumps, target modification, and reduced permeability.

  • Aseptic technique requires a sterile field, sterile gloves, and avoidance of contact with non-sterile surfaces during preparation.

  • Standard precautions apply to all patients: gloves for body-fluid contact, gowns and masks when splash risk exists, and safe sharps disposal.

  • Vaccines induce immunity through inactivated, live-attenuated, toxoid, or subunit antigens; live vaccines are generally contraindicated in immunocompromised patients.