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Chapter Review Steri
Chapter Review Sterile and Nonsterile Compounding
| The technique of mixing two ingredients of unequal quantities is: | Geometric dilution. |
| An ointment base that is anhydrous is: | Oleaginous |
| A single-unit container intended for parenteral administration only is: | Single-dose container. |
| An ointment that is white petrolatum based is: | Oleaginous |
| Oleaginous: | Oily or greasy. |
| An elixir is a: | Clear, sweetened, flavored hydroalcoholic containing water and alcohol. |
| A collodion is: | A topical dosage form containing proxylin and is dissolved in alcohol and ether. |
| The maximum time that can be assigned on the label of a repackaged medication: | 6 months. |
| A piggyback placed in comparison to the primary IV should be: | Higher than the primary IV. |
| In preparation of a 3-1 solution, the order of adding ingredients should be: | Fats, amino acids, and dextrose. |
| Laminar flow hoods should be certified: | Every 2 years. |
| The sensitivity of a class A is: | 6 mg. |
| The spatula that should be used in measuring corrosive ingredients: | A rubber spatula. |
| The term that refers to the space between the HEPA filter and the sterile product is called: | Direct Compounding Area (DCA). |
| The greatest capacity size of a capsule: | Size 0 |
| A pharmacy balance needs certified: | Every year; 12 months |
| The SDS must be provided to the patient when: | Dispensing a hazardous substance. |
| Amples differ from vials because: | Ampules require the use of a filter needle. |