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Questions and Answers
According to Young's Rule, what factors are considered when calculating a child's dose of medication?
According to Young's Rule, what factors are considered when calculating a child's dose of medication?
- The child's weight in pounds and the adult dose.
- The child's weight in kilograms and the adult dose.
- The child's age in months and the adult dose.
- The child's age in years and the adult dose. (correct)
A medication has an adult dose of 75mg. Using Clark's Rule, calculate the approximate dose for a child weighing 40 lbs.
A medication has an adult dose of 75mg. Using Clark's Rule, calculate the approximate dose for a child weighing 40 lbs.
- 20 mg (correct)
- 30 mg
- 10 mg
- 15 mg
Fried's Rule is specifically used to calculate medication dosages for which age group?
Fried's Rule is specifically used to calculate medication dosages for which age group?
- Children between 6 to 12 years old.
- Infants up to 1 year old. (correct)
- Adolescents between 13 to 18 years old.
- Children between 2 to 5 years old.
A 6-month-old infant needs a medication with an adult dose of 100mg. Using Fried’s Rule, what is the calculated dose for the infant?
A 6-month-old infant needs a medication with an adult dose of 100mg. Using Fried’s Rule, what is the calculated dose for the infant?
Using Dilling's Formula, determine the correct dosage of a medication for a 5-year-old child if the adult dose is 50mg.
Using Dilling's Formula, determine the correct dosage of a medication for a 5-year-old child if the adult dose is 50mg.
Why is the body surface area method considered a more reliable approach for dosage calculation compared to age-based rules?
Why is the body surface area method considered a more reliable approach for dosage calculation compared to age-based rules?
If the adult dose of a drug is 200mg and a child has a body surface area of 0.8 m², what would be the child's dose, using the body surface area method? (Assume adult body surface area is 1.73 m²)
If the adult dose of a drug is 200mg and a child has a body surface area of 0.8 m², what would be the child's dose, using the body surface area method? (Assume adult body surface area is 1.73 m²)
Which of the following statements accurately reflects a key consideration in pediatric dosage calculations?
Which of the following statements accurately reflects a key consideration in pediatric dosage calculations?
Which formulation strategy would LEAST address a drug with a highly unpleasant taste?
Which formulation strategy would LEAST address a drug with a highly unpleasant taste?
What is the primary purpose of incorporating disintegrating agents into tablet formulations?
What is the primary purpose of incorporating disintegrating agents into tablet formulations?
Which route of administration is LEAST likely to bypass the first-pass metabolism?
Which route of administration is LEAST likely to bypass the first-pass metabolism?
Which of the following considerations is LEAST relevant when selecting a vehicle for a topical semi-solid dosage form?
Which of the following considerations is LEAST relevant when selecting a vehicle for a topical semi-solid dosage form?
What is the primary reason for using enteric coatings on certain oral drug products?
What is the primary reason for using enteric coatings on certain oral drug products?
Which of the following methods is LEAST effective for achieving sustained release of a drug?
Which of the following methods is LEAST effective for achieving sustained release of a drug?
A pharmaceutical company is reformulating a successful tablet to improve patient compliance. The original tablet had a strong, bitter taste. The reformulated tablet must also disintegrate rapidly for quick absorption. Which of the following strategies would be MOST effective?
A pharmaceutical company is reformulating a successful tablet to improve patient compliance. The original tablet had a strong, bitter taste. The reformulated tablet must also disintegrate rapidly for quick absorption. Which of the following strategies would be MOST effective?
A novel drug is unstable in aqueous solutions but is needed for intravenous administration. Which of the following approaches would be MOST appropriate to formulate this drug?
A novel drug is unstable in aqueous solutions but is needed for intravenous administration. Which of the following approaches would be MOST appropriate to formulate this drug?
A medication's dosage is determined by body surface area (BSA). If a patient with a BSA of 1.5 m² requires a drug with a concentration of 50 mg/m², what is the appropriate individual dose?
A medication's dosage is determined by body surface area (BSA). If a patient with a BSA of 1.5 m² requires a drug with a concentration of 50 mg/m², what is the appropriate individual dose?
A child requires a medication that is typically dosed for adults at 200 mg. If the child has a body surface area of 0.8 m², what would be the appropriate dose for the child, using the body surface area formula?
A child requires a medication that is typically dosed for adults at 200 mg. If the child has a body surface area of 0.8 m², what would be the appropriate dose for the child, using the body surface area formula?
A doctor prescribes amoxicillin for a child with otitis media at a dose of 30 mg/kg/day, divided twice daily (BID). The child weighs 33 lbs, and the amoxicillin suspension is available at a concentration of 250 mg/5 mL. What volume of the suspension should the child receive per dose?
A doctor prescribes amoxicillin for a child with otitis media at a dose of 30 mg/kg/day, divided twice daily (BID). The child weighs 33 lbs, and the amoxicillin suspension is available at a concentration of 250 mg/5 mL. What volume of the suspension should the child receive per dose?
Which characteristic is most crucial for a container intended to maintain the sterility of its contents?
Which characteristic is most crucial for a container intended to maintain the sterility of its contents?
A patient weighing 60 kg requires a drug at a dose of 0.75 mg/kg. The drug is available in a solution of 15 mg/mL. How many milliliters of the solution are needed to provide the correct dose?
A patient weighing 60 kg requires a drug at a dose of 0.75 mg/kg. The drug is available in a solution of 15 mg/mL. How many milliliters of the solution are needed to provide the correct dose?
What is the primary purpose of a 'tamper-evident container' in pharmaceutical packaging?
What is the primary purpose of a 'tamper-evident container' in pharmaceutical packaging?
A pharmaceutical manufacturer is selecting a container for a moisture-sensitive drug product. Beyond preventing moisture loss from the product, which additional container attribute is MOST critical?
A pharmaceutical manufacturer is selecting a container for a moisture-sensitive drug product. Beyond preventing moisture loss from the product, which additional container attribute is MOST critical?
A 4-year-old child weighing 16 kg needs ceftriaxone for meningitis at a dose of 80 mg/kg/day, administered intravenously once daily. If the drug is available at a concentration of 30 mg/mL, how many milliliters should be administered?
A 4-year-old child weighing 16 kg needs ceftriaxone for meningitis at a dose of 80 mg/kg/day, administered intravenously once daily. If the drug is available at a concentration of 30 mg/mL, how many milliliters should be administered?
A pharmacist notices that a new shipment of a liquid medication is packaged in amber-colored glass containers. What concern is the container type addressing?
A pharmacist notices that a new shipment of a liquid medication is packaged in amber-colored glass containers. What concern is the container type addressing?
Why are fillers or diluents added to solid dosage forms when manufacturing drugs, especially when the active drug substance is present in very small quantities?
Why are fillers or diluents added to solid dosage forms when manufacturing drugs, especially when the active drug substance is present in very small quantities?
What is the primary distinction between a 'well-closed container' and a 'tight container' as defined in pharmaceutical packaging standards?
What is the primary distinction between a 'well-closed container' and a 'tight container' as defined in pharmaceutical packaging standards?
Which of the following is the LEAST likely reason for formulating a drug into a specific dosage form?
Which of the following is the LEAST likely reason for formulating a drug into a specific dosage form?
Formulation scientists are developing a new injectable drug that must be packaged in a single-dose container. Which of the following characteristics of the container is MOST critical for maintaining the drug's safety and efficacy?
Formulation scientists are developing a new injectable drug that must be packaged in a single-dose container. Which of the following characteristics of the container is MOST critical for maintaining the drug's safety and efficacy?
A drug is highly susceptible to degradation by hydrolysis. Which strategy would be MOST effective in preventing this degradation during storage and administration?
A drug is highly susceptible to degradation by hydrolysis. Which strategy would be MOST effective in preventing this degradation during storage and administration?
A pharmaceutical company is deciding on the packaging material for a new oral solution. The solution contains a preservative that is known to adsorb onto certain types of plastic. Besides selecting a non-reactive material, what other container property is MOST important to consider?
A pharmaceutical company is deciding on the packaging material for a new oral solution. The solution contains a preservative that is known to adsorb onto certain types of plastic. Besides selecting a non-reactive material, what other container property is MOST important to consider?
A pharmacist receives a bulk shipment of tablets in a container that is labeled as 'well-closed'. Upon inspection, the pharmacist notices a small amount of powder residue at the bottom of the container. While this might not be ideal, what is the PRIMARY expectation that this 'well-closed' container has still met?
A pharmacist receives a bulk shipment of tablets in a container that is labeled as 'well-closed'. Upon inspection, the pharmacist notices a small amount of powder residue at the bottom of the container. While this might not be ideal, what is the PRIMARY expectation that this 'well-closed' container has still met?
Flashcards
Posology
Posology
Deals with the dose or quantity of drug needed to produce a therapeutic effect.
Dose
Dose
The amount of drug administered at one time.
Dosage Determination
Dosage Determination
Determining the amount, frequency, and number of doses for a patient.
Young's Rule
Young's Rule
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Clark's Rule
Clark's Rule
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Fried's Rule
Fried's Rule
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Dilling's Formula
Dilling's Formula
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Body Surface Area Method
Body Surface Area Method
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Enteric Coating
Enteric Coating
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Additive (in Dosage Forms)
Additive (in Dosage Forms)
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Vehicle (in Dosage Forms)
Vehicle (in Dosage Forms)
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Disintegrating Agents
Disintegrating Agents
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Diluents
Diluents
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Colouring Agent
Colouring Agent
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Flavouring agent
Flavouring agent
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Container (Pharmaceutical)
Container (Pharmaceutical)
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Child Dose Calculation
Child Dose Calculation
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Dose by Body Surface Area
Dose by Body Surface Area
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Dose by Body Weight
Dose by Body Weight
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Steps for Dosage Calculation
Steps for Dosage Calculation
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Purpose of Dosage Forms
Purpose of Dosage Forms
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Dosage Forms protect drugs from
Dosage Forms protect drugs from
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Dosage Forms protect drugs from gastric acid
Dosage Forms protect drugs from gastric acid
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Fillers/Diluents
Fillers/Diluents
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Container Rigidity
Container Rigidity
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Container Inertness
Container Inertness
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Environmental Protection
Environmental Protection
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Moisture Retention
Moisture Retention
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Leak Prevention
Leak Prevention
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Well-Closed Container
Well-Closed Container
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Tight Container
Tight Container
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Single-Dose Container
Single-Dose Container
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Study Notes
Posology
- Posology involves the dose or quantity of a drug administered to achieve a therapeutic effect.
- Drug dose refers to the amount of medicinal preparation or radiation given at one time.
- Dosage involves determining the amount, frequency, and number of medicine doses for a specific patient.
Dosage Calculation for Children
- Various rules are employed to calculate dosages for infants and children.
- These methods provide approximate dosages.
- Children may exhibit greater susceptibility to certain drugs compared to adults.
Young's Rule (for Children Aged 1 to 12)
- Formula: Child dose = (age in years / age(years) + 12) multiplied by adult dose
- Example: If an adult dose is 100mg for a child weighing 40kg, the child’s dose using Young's Rule is 37mg.
Clark's Rule (for Children Under 2 Years)
- Formula: Child dose = (Weight in pounds / 150) multiplied by adult dose
- Example: If an adult dose of medication is 30mg for a child who weighs 30lbs, the child’s dose is 6mg.
Fried's Rule (for Infants Up to 1 Year)
- Formula: Infant dose = (Age in months/150) multiplied by the adult dose
- Example: If a physician orders 50mg of diphenhydramine orally every six hours PRN for a four-year-old child, the dose using Fried’s Rule is 16mg of diphenhydramine.
Dilling's Formula
- Formula: Child dose = (Age in years/20) multiplied by adult dose.
- If an adult dose is 100mg for a child weighing 40kg, the child’s dose using Dilling's Formula is 35mg.
Square Meter Surface Area Method
- The square meter surface area method provides a more reliable dosage calculation.
- The average body surface area for adults is 1.73 m².
- Child's dose calculation: Body surface area of child (m²) / 1.73 multiplied by adult dose.
- BSA (m²) can be derived from the square root of: Height (cm) multiplied by Weight (kg) / 3,600
Calculation of Doses for Adults
- Physiological functions, including metabolic rate and kidney functions, often correlate with body surface area.
- Drug doses can use the amount of drug/m² multiplied by body surface area.
- Individual dose can be calculated using the formula: Amount of drug/m² multiplied by Body surface area in m².
- Individual's dose is often given in mg/kg multiplied by body weight in kg.
Dosage Form Necessity
- Many drugs are administered in small (milligram) quantities, necessitating precise weighing.
- Low dosage of potent drugs requires solid forms such as tablets and capsules, prepared with fillers or diluents to increase size for easy handling.
- Dosage forms ensure safe and convenient administration of accurate drug doses
- Dosage forms protect the drug from destructive elements like atmospheric oxygen, moisture, oxidation, hydrolysis, and reduction, often with coatings
- Enteric coatings protect drugs from degradation by gastric acid after oral administration, dissolving in alkaline pH instead
- Dosage forms can mask bitter, salty or offensive taste or odors through capsules or flavored syrups.
- Dosage forms allow for insoluble or unstable drugs to be administered as liquid suspensions
- Dosage forms enable drugs to be administered in clear liquid solutions
- Dosage forms permit rate-controlled and sustained drug release, such as controlled-release tablets
- Dosage forms enable drug action through topical application, e.g., creams and transdermal patches
- Dosage forms facilitate drug action via insertion into body cavities, like suppositories
- Dosage forms achieve drug action by direct delivery into the bloodstream or body tissues via injections.
- Dosage forms enable drug action through inhalation therapy using inhalation aerosols
Additives in Dosage Forms
- Dosage form action and form depends on the additives included
- Additives refer to non-drug components with specific functions within the formulation
Classifications of Additives included in Formulations
- Vehicles refer to solid, semisolid, or liquid materials that assist in drug formulation.
- Solvents, aqueous or non-aqueous, are used to dissolve drugs.
- Bases are semi-solid vehicles that incorporate drug substances in formulations like ointments, pastes, and suppositories..
- Diluents increase bulk or reduce drug concentration.
- Disintegrating agents facilitate disintegration of ingested dosage forms into smaller particles.
- Colouring agents enhance the dosage form's appearance with appropriate color.
- Flavouring agents give a pleasant flavour, especially important in liquid dosage forms.
- Sweetening agents impart a sweet taste to preparations.
- Manufacturing additives improve the manufacturing process
Dosage Form Packaging
- Proper packaging, labeling, and storage maintain pharmaceutical product stability and effectiveness.
- Specifications vary for parenteral, non-parenteral, pressurized, and bulk containers made of glass, plastic, and metal.
- A container serves as a device that holds the pharmaceutical preparation.
Container Features
- Containers should be rigid to withstand normal handling and prevent damage.
- Container material must not react unfavorably with the contents.
- Containers should protect contents from environmental deterioration caused by oxygen and moisture.
- Containers should prevent moisture loss
- Containers must prevent leakage of contents.
- Containers must impede the entry of dirt, chemicals, or microbial contamination.
- Containers should be sterilizable without altering its integrity.
- Containers should provide protection from light when necessary.
- Ideally, the container should not absorb medicaments or additives from the contents.
- The container should not impart anything to the contents.
- The container must be easy to label.
- The container must be pharmaceutically elegant
Container Types classified by Protection Ability
- Well-closed containers protect contents from external solids and loss, functioning under normal handling, storage, and shipping conditions.
- Tight containers protect contents from external liquid, solid, and vapor contamination, preventing changes due to efflorescence, deliquescence, or evaporation.
- Hermetically sealed containers prevent air and gases from passing through, maintaining sterility for sterile preparations.
- Light-resistant containers protect contents from photochemical deterioration, using amber glass or opaque plastic.
- Temper-evident containers feature a mechanism that reveals irreversible opening.
- Child-resistant containers are designed to be difficult for children to open.
Container Types classified by Number of Doses
- Single-dose containers provide a single dose of medication, are not resealable to maintain sterility, e.g., ampoules.
- Multi-dose containers allow successive dose withdrawals without compromising the strength or purity of the remaining contents and are hermetically sealed, e.g., vials.
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Description
Explore pediatric dosage calculations using Young's, Clark's, and Fried's Rules. Learn about body surface area methods for accurate medication dosing in children. Examples included.