In each blank, try to type in the
word that is missing. If you've
typed in the correct word, the
blank will turn green.
If your not sure what answer should be entered, press the space bar and the next missing letter will be displayed. When you are all done, you should look back over all your answers and review the ones in red. These ones in red are the ones which you needed help on. Question: Which law made requirements for OTC products?Answer: FDA-Food, Drug, and Cosmetic Question: When a drug is in the process of being made or discovered, this application must be filed with the FDA to prove and safety before becoming commercially available. Answer: NDA- New Drug Question: contains decomposed substanceAnswer: adulterated Question: the label may be or misleadingAnswer: mis-branding Question: The Durham-Humphrey is also called theAnswer: drug amendment Question: proper and directions are absent
Answer: mis-branding Question: manufacturer name and of business absentAnswer: mis-branding Question: stock label fails to say "warning-may be forming" if med is habit formingAnswer: mis-branding Question: has been packaged under unsanitary conditionsAnswer: adulterated Question: product has different or purity than whats indicated on labelAnswer: Question: What is the that requires manufacturers to dispense medications with labels to the patient?Answer: Kefauver-Harris Question: What are requirements for manufacturers as outlined by the Kefauver-Harris ? Answer: 1. requires manufacturers to annually
2. be inspected every 2 years
3. report any drug interactions Question: all medication on the U.S market to be pure, safe, and effectiveAnswer: -Harris Amendment Question: PPI's are regulated by the FDA. What are ?Answer: Patient Inserts Question: PPI's MUST be to patients receiving what medications?Answer: oral contraceptives
estrogen
progestin
isotetinoin (accutane)
intrauterine ( IUD's)
inhalers Question: on the PPI MUST include:Answer: product description
indications for (when/ and what it interacts with)
warnings (extreme side-effects)
precautions (less sever side-effects)
Dose (how much and how often) Question: The Occupational and Safety Act of 1970 gave rise Answer: OSHA- Occupational and Health Administration Question: What does OSHA do?Answer: ensures job safety and an injury system for job related injuries or illnesses Question: OSHA requires the toAnswer: post the number to poison control
have a reference guide for
must have Material Safety Data Sheets (MSDS) for any "hazardous materials" in pharmacy Question: The Poison Prevention Packaging Act was to Answer: accidental poisonings in children Question: The Poison Prevention Act pharmacies toAnswer: use resistant containers Question: Exceptions to the Answer: medical meds
written requests from DRs or patients
Question: According to the PPA, OTC meds Answer: be labeled "package not resistant" of the package is not child-resistant. Question: Examples of medication from the PPA include:Answer: nitroglycerin sublingual (for chest pain)
betamethasone, , methylprednisolone (<85 mg), oral contraceptives, pancrelipase, cholestyramine Question: A Log must include: Answer: date of sale
name and address of and quantity of poison dispensed
full name of dispenser Question: Poisonous substances must be with: Answer: complete name of poison
the word boldly imprinted on label
place of business of the seller
proper directions of use Question: What is of Ipecac and how much should be ingested?Answer: used in the emergency treatment of kinds of poisoning
15ml or 1 tablespoon Question: What does Charcoal do?Answer: absorbs and eliminates poison in the body
(not to be taking with Syrup of Ipecac as this will not work or make the person vomit) Question: Who the Controlled Substances Act of 1970? And what do they do?Answer: The DEA- regulates use and distributes drugs with high abuse potential and/or into one of the five schedules Question: Every pharmacy must make a complete inventory of controlled substances every ___ years and kept on record for ___ .Answer: two, Question: A DEA contains how many letter and numbers?Answer: Two letters, numbers Question: DEA letters Answer: start with A, B or M for letter is Drs initial to last name Question: Is this DEA valid? Why?
BB10066123Answer: Do math and . Question: Can CII medications be ? Answer: No, new prescription is with every fill Question: CIII and CIV scripts cannot be filled more than ___ times in a ____ month period.Answer: Five, Six (also CVs) Question: CII and CIV can be filled verbally with what exception? Answer: A written script verbal. Question: CV meds can be without script is state allows but this mustAnswer: be in the CV log. Question: Schedule I medications Answer: not accepted for medical use in the U.S
lack of accepted safety use under medical supervision, and a high for abuse Question: Some examples of CI meds :Answer:
lysergic acid (LSD)
marijuana
peyote
methaqualone (Ecstasy) Question: II medications Answer: have a high for abuse which may lead to sever psychological or physical dependence. Question: Some examples of CII meds : Answer: hydromorphone
methadone
meperidone
oxycodone
fentanyl
morphine
opium
codeine
hydrocodone Question: Schedule III Answer: has a potential for abuse, less than CI and CII. May lead to moderate or low physical dependence or high dependence. Question: Some of CIII meds include:Answer: products containing not more than 90 milligrams of codeine per dosage unit --Tylenol 3 & 4, Question: IV medicationsAnswer: low potential for Question: Some of CIV meds include: Answer: Xanax, Klonopin, , Ativan, Restoril Question: V medicationsAnswer: have a low potential for abuse, contain limited quantities of narcotics Question: Some examples of CV meds : Answer: Robitussin AC
Phenergan w/ codeine
Ezogabine
cough preparations containing note more than 200 mg of per 100 ml or per 100 grams Question: of Pharmacy Technician duties:Answer: -varies by state
cannot take verbal scripts
cannot give consultations
cannot take or transfer Question: Drugs are ifAnswer: it was improperly made or labeled and severe adverse reactions Question: I drug recall:Answer: exposure will cause extreme health hazards or Question: Class II drug :Answer: exposure may cause temporary health Question: Class III drug :Answer: not likely to cause health Question: OBRA is also as theAnswer: Omnibus Act of 1990 Question: The of OBRA: Answer: directed toward pharmacists but require technician quality of drug therapy and saves healthcare costs
(requires pharmacists to give consultations) Question: OBRA counseling that must include:Answer: name and description of form, dose, route of administration, and duration of therapy
special directions, precautions
side effects and ways to prevent
techniques for self-monitoring
storage
refill info
action to take if missed dose |
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