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This deck focuses on Parenteral Medications, giving you a quick way to review the definitions, rules, and examples that matter most for NAPLEX.
Study Parenteral Medications in NAPLEX with focused flashcards that help you recognize the idea, recall the key rule, and apply it in practice-style prompts.
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What does the term "vesicant" mean for an IV medication if extravasation occurs?
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Can cause tissue necrosis and severe local injury. Vesicants damage tissues upon extravasation due to their irritant properties, leading to blistering and potential long-term injury.
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This deck focuses on Parenteral Medications, giving you a quick way to review the definitions, rules, and examples that matter most for NAPLEX.
Work through these flashcards in short sessions. Try to answer each prompt before flipping the card, then revisit any cards you miss until the explanation feels automatic.
Answer: Can cause tissue necrosis and severe local injury. Vesicants damage tissues upon extravasation due to their irritant properties, leading to blistering and potential long-term injury.
Answer: Container intended for one-time use for a single patient/procedure. USP <797> specifies single-dose containers to prevent microbial growth by limiting use to one entry, ensuring sterility for individual patient needs.
Answer: 0.22 μm. The 0.22 μm size effectively removes bacteria and small particles from aqueous solutions without impeding flow.
Answer: mL/hr=hrmL. The formula derives the rate by dividing total volume by infusion time for consistent delivery.
Answer: 1.2 μm. Lipids require larger pores like 1.2 μm to pass through without being trapped, unlike smaller filters for aqueous solutions.
Answer: A CSP prepared for immediate administration with minimal delay. USP <797> defines immediate-use CSPs as those prepared aseptically outside controlled environments for administration starting within 4 hours to reduce microbial contamination risk.
Answer: Risk of benzyl alcohol toxicity (gasping syndrome). Benzyl alcohol in bacteriostatic water can cause metabolic acidosis and respiratory distress in neonates due to immature liver function.
Answer: It must not be given IM, SC, intrathecal, or epidural. The label restricts administration to IV to prevent adverse effects like tissue irritation or inefficacy associated with other routes.
Answer: 28 days after initial entry (unless manufacturer states otherwise). The 28-day BUD balances preservative efficacy against contamination risk, aligning with USP <797> guidelines unless shorter stability is indicated by the manufacturer.
Answer: Approximately 900 mOsm/L (institution-specific limits may vary). Osmolarity limits for PPN prevent vein irritation and phlebitis, with ~900 mOsm/L as a common threshold based on institutional protocols.
Answer: Sterile water for injection (SWFI). SWFI lacks preservatives like benzyl alcohol, reducing toxicity risks in vulnerable patients compared to bacteriostatic water.
Answer: To remove particulates (and sometimes air/microprecipitates) from the infusion. In-line filters capture contaminants to ensure infusion safety, particularly for solutions prone to particle formation.
Answer: 5 mL/hr. Dividing dose rate by concentration ensures the infusion delivers the ordered amount per hour.
Answer: 125 mL/hr. Dividing volume by time yields the rate, ensuring accurate delivery over the specified period.
Answer: Central venous access. Central access reduces extravasation risk by diluting vesicants in larger blood volumes, unlike peripheral veins.
Answer: Container that allows repeated entries and usually contains a preservative. USP <797> allows multiple-dose containers for repeated access due to preservatives that inhibit microbial growth, extending usability beyond single entry.
Answer: mL/hr=mg/mLmg/hr. The formula determines volume rate by dividing desired dose rate by solution concentration for therapeutic accuracy.
Answer: Preservative-free 0.9% sodium chloride (or preservative-free SWFI if specified). Preservatives can cause neurotoxicity in the CSF, so preservative-free diluents ensure safety for intrathecal routes.
Answer: gtt/min=minmL×gtt/mL. The formula accounts for drop factor to convert volume over time into countable drops per minute.
Answer: 5 g per 100 mL. D5W provides 5% dextrose by weight, equating to 5 grams per 100 mL for caloric support in parenteral nutrition.
Answer: 0.9% sodium chloride (normal saline). 0.9% sodium chloride matches plasma osmolarity at approximately 308 mOsm/L, minimizing cellular damage during infusion unlike hypotonic 0.45%.
Answer: 50 gtt/min. Multiplying volume by drop factor and dividing by minutes provides the precise manual adjustment rate.
Answer: IM. IM route allows slow absorption of oil-based formulations, providing sustained release unlike rapid IV dispersion.
Answer: 2 mg/mL. Dividing total drug amount by final volume gives concentration for dosing calculations.
Answer: Neurotoxicity; neuraxial products should be preservative-free. Preservatives in neuraxial medications can irritate neural tissues, leading to inflammation or damage in the spinal area.