Afghanistan Pharmacy Technician Exit Exam study materials
Afghanistan Pharmacy Technician Exit Exam study resources

Afghanistan Pharmacy Technician Exit Exam flashcards

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32 cards. Read the term and the definition here. The deck at the top of this page is optional.

Valid prescription elements
Prescriber name and signature, patient name, drug name, strength, dosage form, quantity, directions, and date; missing elements make the prescription invalid and require clarification.
Controlled drug prescription rules
Schedule II-type medicines require a written prescription, no refills, and dispensing within the legally defined time window; records of receipt and supply must be kept.
Generic substitution condition
A pharmacist may substitute a generic only when law permits, the prescriber has not written dispense-as-written, and the patient is informed of the substitution.
Technician scope of practice
Technicians prepare, label, and manage stock under pharmacist supervision; counseling, clinical verification, and final release remain the pharmacist's legal responsibility.
Beta-lactam mechanism
Penicillins and cephalosporins inhibit bacterial cell wall synthesis, making them bactericidal; allergy cross-reactivity must be checked before dispensing.
Opioid adverse effects
Mu-receptor opioids cause respiratory depression, constipation, sedation, and dependence; naloxone is the antidote for overdose.
Warfarin versus heparin monitoring
Warfarin inhibits vitamin K-dependent clotting factors and is monitored by INR; heparin is monitored by aPTT.
Tuberculosis combination therapy
Combination regimens such as isoniazid, rifampicin, pyrazinamide, and ethambutol prevent resistance; isoniazid can cause peripheral neuropathy.
Dose calculation formula
Dose = (desired dose / stock strength) x stock volume, with all units converted to the same system before calculation.
Percentage solution meaning
Percent w/v is grams per 100 mL, percent w/w is grams per 100 g, and percent v/v is mL per 100 mL; the type must be stated on the label.
Dilution equation
C1 x V1 = C2 x V2: the concentration of the stock times its volume equals the final concentration times the final volume.
IV drip rate formula
Drops per minute = (volume in mL x drop factor in drops/mL) divided by time in minutes.
Body surface area formula
Mosteller method: BSA in square meters = square root of (height in cm x weight in kg / 3600); used for mg/m2 dosing.
Prescription processing sequence
Validate the prescription, check allergies and patient record, prepare, label, obtain pharmacist verification, then release with counseling.
Required label content
Patient name, drug name and strength, directions, quantity, date, pharmacy identity, and any cautionary or storage statements.
Abbreviations to avoid
Write 'units' instead of 'U', 'once daily' instead of 'QD' or 'OD', and never add trailing zeros such as 5.0 mg.
Final dispensing check
Compare the prescription against the prepared product for drug, strength, dosage form, quantity, label details, and expiry date before release.
Enteric-coated tablet rule
Enteric coatings protect against gastric acid; these tablets must not be crushed or chewed, or the coating's protective function is lost.
Suspension handling
Suspensions are biphasic and must be shaken before each dose to redistribute the dispersed particles and deliver a uniform dose.
Geometric dilution method
A small quantity of potent powder is mixed with an equal volume of diluent, then repeatedly doubled until the full diluent is incorporated uniformly.
Beyond-use date definition
The date after which a compounded preparation must not be used, based on its stability, preservative content, and storage conditions.
Pharmacokinetic interaction
An interaction that alters absorption, distribution, metabolism, or excretion, such as enzyme inducers lowering the effect of warfarin.
MAOI tyramine interaction
Monoamine oxidase inhibitors combined with tyramine-rich foods or sympathomimetics can precipitate a hypertensive crisis.
Missed dose counseling
Advise the patient to follow the product's specific missed-dose rule and never to double the next dose to make up for a missed one.
Photosensitivity counseling
Tetracyclines and some other drugs cause photosensitivity; patients should protect skin from sunlight and report unusual reactions.
First Expiry First Out
FEFO rotation dispenses the stock with the earliest expiry date first, reducing waste; FIFO applies when expiry dates are uniform.
Cold-chain storage range
Products such as insulin and some vaccines require 2-8 degrees C with continuous temperature monitoring and a documented excursion procedure.
Quarantine of recalled stock
Expired, damaged, or recalled stock must be segregated in a labeled quarantine area and disposed of under national regulations.
Signs of drug quality failure
Discoloration, changed odor or texture, caking, leakage, cracked tablets, and particulate matter in solutions indicate a defective product.
Hand hygiene importance
Hand hygiene with soap and water or alcohol rub before and after patient contact is the single most effective measure against cross-infection.
Sharps handling rule
Sharps must never be recapped by hand; they are placed immediately into a puncture-resistant, labeled sharps container.
Antimicrobial resistance prevention
Complete prescribed courses, avoid unnecessary antibiotics, and never share antibiotics; these actions slow the emergence of resistant organisms.