Best answer
Quiz yourself by thinking what should be in
each of the black spaces below before clicking
on it to display the answer.
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| The FDA requires how many phases of testing humans? | 3 phases.
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| The main purpose of Phase 2 clinical trials is | effectiveness
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| several hundred to several thousand people | Phase 3 clinical trial generally have...
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| After a patent has expired for a med, other mfg may copy the drug and release it under | generic name
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| A script to dispense Plan B | is required for pt under 17yrs of age
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| MedWatch | The FDA reporting system for adverse effects that occur from use of approved drugs
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| A tech could be prosecuted for misconduct if incorrectly labeled a prescription | is negligence
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| The first digit 5 digits of the NDC | is mfg
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| The last digit of NDC are indicative. | the package size
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| Federal law requires pharmacies to have available for inspection | Copy 3 of DEA form 222 for 2 yrs.
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| Which book is used for FDAs list of approved generic equivalents | Orange Book
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| Scheduled C2 | meperidine
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| HIPAA | privacy rules are observed for PHI
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| Must be administered in a glass IV container | Nitroglycerin
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| the sale of this drug is restricted by CMEA | Claritin-D24
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| CMEA allows what max amount sold per month | 15
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| Of all the Recalls, the most important in all involving: Dr, pharmacy, pt due to drug potential/serious harm | Class 1 Recall
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| Accutane | associated with iPLEDGE
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| Whom and how receives Copy 2 of DEA Form 222 | it is forwarded to DEA
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| Exempt Narcotics | are DEA Schedule C5
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| They are regulated for dosage units sold within 48hrs | Exempt Narcotics
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| Federal law requires pharmacies to keep | Copy 3 of DEA Form 222
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| MedWatch Form 3500 | reports adverse reactions to drugs
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