Dispensing and Adverse Drug Reactions (ADR) Flashcards

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Vocabulary flashcards covering dispensing guidelines, prescription components, drug incompatibilities, drug interactions, and adverse drug reaction (ADR) classifications based on Module 3.

Last updated 1:21 PM on 9/4/26
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36 Terms

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Dispensing (AO 63 s.1989)

The act by a validly registered pharmacist of filling a prescription or order.

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Good Pharmacy Practice (GPP)

The practice of pharmacy that responds to the needs of the people who use the pharmacists' services to provide optimal, evidence-based care (FIP/WHO).

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Prescription (AO 63 s.1989)

A written order and instruction of a validly registered physician, dentist, or veterinarian for the use of a specific drug product or medical device for a specific patient.

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Prescription Parts Diagram

A sample prescription layout illustrating the 8 required components: prescriber info (1), date (2), patient info (3), superscription Rx (4), inscription (5), subscription (6), transcription/sig (7), and prescriber signature with license numbers (8).

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Dangerous Drugs Prescription

A yellow-triplicate prescription form issued by PDEA requiring an S2 license, where partial filling is allowed but refills are prohibited.

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S2 License Number Format

A code structure displaying permanent number, year issued, transaction status (NN=New, RR=Renewal, EE=Exempt), practitioner type (MM=Physician, DD=Dentist, VV=Veterinarian), region paid, loss status, and control number.

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Erroneous Prescribing Offense

A generic prescribing offense where the brand name precedes the generic name, generic name is in parentheses, or brand name is not in parentheses; the drug is dispensed and reported.

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Violative Prescribing Offense

A generic prescribing offense where only the brand name is written, brand name is more prominent than generic name, or instructions prevent substitution; the drug is not dispensed and reported.

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Impossible Prescribing Offense

A generic prescribing offense where generic/brand names are illegible, generic name does not match brand name, or drug is unregistered with Philippine FDA; the drug is not dispensed and reported.

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Tall-Man Lettering

A practice recommended by US FDA and ISMP that uses capitalized letters to differentiate look-alike sound-alike (SALAD) drug names, such as acetaZOLAMIDE vs. acetoHEXAMIDE.

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Terminal Sterilization Methods

Sterilization techniques including moist heat (autoclave at 121oC121^\text{o}\text{C}, 15 psi15\text{ psi}, 1530 mins15\text{--}30\text{ mins}), dry heat (oven at 160oC160^\text{o}\text{C}, 24 hrs2\text{--}4\text{ hrs}), membrane filtration (0.2-micron0.2\text{-micron} filter), gas (ethylene oxide), and ionizing radiation (gamma rays).

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Physicochemical Incompatibility

A drug incompatibility occurring outside the body that is directly observable, manifested by precipitate formation, color/odor change, gas evolution, or physical state changes.

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Deliquescent

The property of a substance that absorbs atmospheric moisture and dissolves in it, such as NaOHNaOH, KOHKOH, or NH4ClNH_4Cl.

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Efflorescent

The property of a hydrated substance that releases moisture into the surrounding air, such as CuSO4×H2OCuSO_4 \times H_2O, Na2CO3×10H2ONa_2CO_3 \times 10H_2O, or CaSO4×2H2OCaSO_4 \times 2H_2O.

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Eutexia

Melting point depression leading to liquefaction when two solid substances (such as camphor and menthol) are mixed together.

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Syneresis

The loss of water or liquid exuding from a gel dosage form due to shrinkage.

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Precipitant Drug

In a drug interaction, the drug that causes the interaction or alters the effect of another drug.

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Object Drug

In a drug interaction, the drug whose action, concentration, or effect is altered by the precipitant drug.

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Enzyme Inhibitors and Inducers

Hepatic metabolic modulators summarized by mnemonics: inhibitors SICKFACES.COM GQ (e.g., Sodium valproate, Cimetidine, Ketoconazole) decrease metabolism; inducers CRAPGPT S (e.g., Carbamazepine, Rifampicin, Phenytoin) increase metabolism.

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Pharmacodynamic Addition

A pharmacodynamic interaction where the combined response of two drugs equals the sum of their individual effects (1+1=21 + 1 = 2).

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Pharmacodynamic Synergism

A pharmacodynamic interaction where the combined effect of two drugs is greater than the sum of their individual effects (1+1>21 + 1 > 2), such as sulfamethoxazole and trimethoprim.

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Pharmacodynamic Potentiation

A pharmacodynamic interaction where a drug with no direct effect increases the activity of another drug (1+0=21 + 0 = 2), such as amoxicillin combined with clavulanic acid.

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Pharmacodynamic Antagonism

A pharmacodynamic interaction where the effect of one drug reduces or cancels the effect of another drug (1+1=01 + 1 = 0), which can be pharmacologic or physiologic.

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Adverse Drug Event (ADE)

Any untoward medical occurrence during treatment with a drug, which does not necessarily have a causal relationship with the drug.

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Adverse Drug Reaction (ADR)

Any response to a drug that is noxious and unintended, occurring at doses normally used in humans for prophylaxis, diagnosis, or therapy.

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Side Effect

Any unintended effect of a drug occurring at normal doses that is related to its pharmacological properties.

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Toxicity

Any noxious and unintended or intended response to a drug occurring at doses higher than normally used in humans.

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Medication Error

A preventable event that may lead to inappropriate medication use or patient harm while the medication is under the control of the health care professional, patient, or consumer.

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Pharmacovigilance

The science and activities relating to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems (WHO).

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Type A ADR (Augmented)

An adverse drug reaction that is common, predictable, dose-dependent, and related to the drug's pharmacology, including side effects and toxicity.

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Type B ADR (Bizarre)

An unpredictable, dose-independent, and uncommon idiosyncratic reaction categorized into Type I (IgE-mediated), Type II (cytotoxic), Type III (immune complex), and Type IV (T-cell mediated).

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Type C ADR (Continuous)

An adverse drug reaction related to cumulative dose and duration of drug use, such as adrenal suppression from steroids or nitrate tolerance.

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Type D ADR (Delayed)

An adverse drug reaction that manifests long after exposure, such as teratogenicity (e.g., phocomelia from thalidomide, spina bifida from valproic acid) or carcinogenicity.

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Pregnancy Safety Categories

Classification system for drug safety in pregnancy ranging from Category A (safe) and Category B (e.g., paracetamol, amoxicillin) to Category D (benefits > risk) and Category E/X (unsafe, contra-indicated, e.g., thalidomide, isotretinoin).

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Type E ADR (End of Use)

An adverse drug reaction occurring upon sudden termination or discontinuation of therapy, managed by dose tapering (e.g., opioid withdrawal, rebound hypertension from clonidine).

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Type F ADR (Failure of Therapy)

An adverse drug reaction characterized by an unexpected loss of drug efficacy, primarily caused by antimicrobial resistance (AMR).