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Iowa 2014 pharmacy law EXAM

Quiz yourself by thinking what should be in each of the black spaces below before clicking on it to display the answer.
        Help!  

Question
Answer
Display of license - what is required?   show
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What info is available for public inspection for each person licensed by the board?   show
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Family planning clinic - is it regulated by Iowa code (155a)?   show
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Control substance -definition   show
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show Pharmacist designated on a pharmacy license as the pharmacist who has the authority and responsibility for the pharmacy's compliance with the laws and rules pertaining to the practice of pharmacy  
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show 1.apply to the board-subject to approval 2.register during training 3.must meet standards - registrations may be revoked, suspended or denied if in violation of the laws in any state relating to prescription drugs, controlled substances or non rx drugs.  
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Pharmacist-intern - definition   show
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show any pharmacist licensed to practice pharmacy whose license is current and in good standing.  
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show no  
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show 1.licensed pharmacist 2. responsible for initialing and dating competencies obtained by intern and for completing affidavits for number of hours and dates for intern's training 3. responsible for all functions performed by intern  
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how many interns may preceptor supervise concurrently?   show
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show establish competency and identification,tracking and disciplinary action for violations  
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who is ultimately responsible for the actions of a pharmacy tech?   show
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show complete application for registration within 30 days of accepting employment in an Iowa pharmacy (board shall receive an application before 30 days expire)  
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technician training   show
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show 12 month to complete ICPT or PTCB Pharmacy Technician Certification Board (PTCB ) and the Institute for the Certification of Pharmacy Technicians (ICPT).  
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pharmacist license - components   show
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show The NDC is a unique 10-digit identifier assigned to each medication. It has 3 segments: The Labeler code identifies the company that manufactures or distributes the drug. The Product segment identifies the strength, dosage form, and formulation. The Packa  
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show Orphan drugs are for rare diseases, which means the disease effects less than 200,000 people in the US. The Orphan Drug Act of 1983 is meant to encourage companies to development drugs for these diseases.  
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purpose of Phase 3 clinical studies   show
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A drug is found to be under-strength, although it is not used to treat a life-threatening disease. What type of recall will be required?   show
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show It is legally owned by the pharmacy and should not be given to the patient. A copy of the prescription should be offered if the patient requests it.  
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show The excipient is the inactive substance that carries the active ingredients, and they do not need to be identical for a drug to be a pharmaceutical equivalent.  
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Which of the following would not be a privacy violation under HIPPA? I. Leaving message re:rx with the patient's spouse. II. Allowing a pharm sales rep to review patient's rx files III. Mailing a prescription reminder to a patient in a sealed envelope.   show
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there is evidence that a new drug could create a risk to the human fetus based on investigational studies. However,benefits of the drug may justify use of the drug in pregnant women despite risks. What pregnancy category would this drug be classified in?   show
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show Schedule I controlled substances are those with a high potential for abuse, no accepted medical use, and a lack of accepted safety information.  
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show anabolic steroids and marinol(Morphine is a Schedule II controlled substance)  
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tech check tech program   show
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show Required hours of internship 1500 hours total: 1250 hours - college based clinical program 250 hours - under the supervision of a preceptor in a licensed pharmacy  
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show Permanent closing Change of ownership,location,pic Sale/transfer of drugs on closing/change ownership Change of legal name Theft or significant loss of controlled Disasters etc affecting strength, purity, or labeling of drugs, medications, devices,  
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show A pharmacist shall report in writing to the board within 10 days a change of name, address, or place of employment  
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notification to the board : wholesaler   show
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validity of rx based on:   show
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show The date of issue Name and address of patient Name, strength, and quantity of drug, medicine, or device Directions for use Name, address, and written signature of practitioner DEA # if controlled substance  
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What additional items are required on a faxed prescription?   show
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What 2 items are not required on an oral prescription called in?   show
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show 12 refills during 18 month (in practice- only 12 month)  
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show rxt is unable to contact MD with reasonable effort may create patient suffering RXT informs the patient or the patient's agent at the time of dispensing, and the practitioner re: reauthorization is required rx may be refilled once till authorization  
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CS : SCHEDULES FIORINAL   show
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show UP TO 60 DAYS IF PATIENT IS IN LTCF OR TERMINALLY ILL . DOCUMENT DATE, QTY DISPENSED , QTY REMAINING, ID OF DISPENSING PHARMACIST ON THE BACK OF RX  
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show UP TO 72HRS - IF LATER- OBTAIN NEW RX  
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show ONLY IF PHARMACY CLOSED ONLY AUTHORIZED PERSON WRITTEN DR ORDER PLACED INSIDE LOG MAINTAINED  
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show Yes (ephedrine, PSE, and PPA are schedule V)  
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show 18 months non-CS , 6 months limit on rx in controlled substance C-III to C-V C-II- NA  
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Does state allow sale of C-V preps OTC?   show
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show Yes- C-II to C-IV  
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Marijuana schedule   show
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show Dronabinol (Tetrahydrocannabinol (THC) ) C-III (state)  
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Ephedrine, phenylpropanolamine, pseudoephedrine CS SCHEDULE? ELECTRONIC REAL TIME RECORDS?   show
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show 3600 MG IN 24HRS 1 PACKAGE IN 24 HRS 7500 MG IN 30DS  
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show Purchaser must be at least 18 years of age and present a government‐issued photo ID, including proof of age  Pharmacist is responsible for verifying name and that photo on the ID matches the purchaser  
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RESTRICTIONS ON SALE Ephedrine, phenylpropanolamine, pseudoephedrine -CAN MORE THAN 7500 MG BE SOLD IN 30DS?   show
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Ephedrine, phenylpropanolamine, pseudoephedrine   show
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Ephedrine, phenylpropanolamine, pseudoephedrine PTS PRINT OUT AVAILABLE?   show
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CS registration   show
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show C-IV  
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Lomotil (diphenoxylate w/ atropine) Promethazine/codeine elixir(PHENERGAN)   show
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CAN C-II RXS BE FAXED TO PHARMACY?   show
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show 1. Narcotic CII to be compounded for direct parenteral (IV, IM, SC, epidural) administration to a patient 2. For resident of a long‐term care facility 3. For a hospice patient  
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adding 1000 mg of codeine to tylenol with codeine compound 120/12mg/5ml makes final mix schedule ...   show
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show OBRA-90 -DOCUMENT SUCH REFUSAL , NO OBLIGATION TO COUNSEL IF DOCUMENTED REFUSAL  
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MID LEVEL PRACTITIONERS ARE..   show
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C-V   show
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C-V   show
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C-V   show
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C-V   show
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OTC SALE OF C-V: QTY,WHO?   show
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show CODEINE CONTAINING (ROBITUSSIN AC ) MAX 4OZ=120ML IN 48HRS  
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morphin-CS?   show
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show PHARMACY MAY SEND AT ANY TIME TO REVERSE DISTRIBUTOR, REVERSE DISTRIBUTOR MUST ISSUE DEA-222 FORM TO PHARMACY  
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DEA-41 FORM   show
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show NAME,DOSAGE FORM,STRENGTH, QUANTITY, DATE WHEN SENT to reverse distributor  
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show ONCOLOGY AND HAZARDOUS -COMPOUNDED UNDER VERTICAL LAMINAR FLOW IN CLASS II BIOLOGY SAFETY CABINET  
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show TREATMENT OF ADDICTION/PRESCRIBING CS C-II (IE METHADONE) APPLICANT FILLS DEA FORM 363  
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TO PROVIDE MAINTENANCE AND ADDICTION TREATMENT PRESCRIBER MUST:   show
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PRESCRIBE CS CIII-V FOR ADDICTION TREATMENT DR.MUST:   show
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BUPRENEX USE :   show
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3-DAY RULE (OR 72 HOUR RULE)   show
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show PATIENT MUST BE REGISTERED IN ADDICTION TREATMENT PROGRAM  
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REFILLS   show
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show CONTINUOUS QUALITY IMPROVEMENT PROGRAM  
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show INCORRECT DRUG INCORRECT DRUG STRENGTH INCORRECT DOSAGE FORM DRUG RECEIVED BY WRONG PATIENT INADEQUATE OR INCORRECT PACKAGING, LABELING OR DIRECTIONS ANY INCIDENT RELATED TO RX DISPENSED THAT HAS POTENTIAL TO RESULT IN SERIOUS HARM TO THE PATIENT  
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show EACH PHARMACY AND PIC - POLICIES AND PROCEDURES ,TRAINING ,ANALYZING DATA COLLECTED - AN MIN ANNUAL MEETING WITH RELATED PERSONNEL  
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show PERSONNEL TRAINED TO INFORM PHARMACIST ON DUTY NOTIFYING PATIENT OR CAREGIVER NOTIFYING PRESCRIBER COMMUNICATING DIRECTIONS TO CORRECT THE ERROR COMMUNICATING INSTRUCTIONS FOR MINIMIZING ANY NGATIVE IMPACT  
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CQI RECORDS   show
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show AUTHORIZED PHARMACIST MEANS IOWA LICENSED PHARMACIST WHO HAS MET THE REQUIREMENTS  
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WHAT ARE THE REQUIREMENTS FOR VACCINE ADMINISTRATION   show
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show PROTOCOL SIGNED BY LICENSED IOWA PRESCRIBER SHALL EXPIRE NO LATER THAN 1 YEAR FROM EFFECTIVE DATE BE EFFECTIVE FOR PATIENTS WHO HAVE NO CONTRAINDICATIONS AND MEET CDC (CENTRE FOR DISEASE CONTROL AND PREVENTION) CRITERIA  
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IN CASE OF SERIOUS COMPLICATION RE VACCINE ADMINISTRATION   show
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if closing pharmacy -notify who -time frame   show
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show RX DRUGS TRANSFERED-COMPLETE INVENTORY AS OF CLOSE OF BUSINESS.=ENDING INVENTORY =ADDITIONAL OR STARTING INVENTORY FOR RECEIVING PHARMACY  
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CLOSING PHARMACY - INVENTORY (CONT.)   show
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show RECORDS PERTAINING TO TRANSFER OF CS -SELLER TO BUYER- ON THE DATE OF SALE  
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show WITHING 10 DAYS -RETURN PHARMACY LICENSE CERTIFICATE, STATE CSA REGISTRATION CERTIFICATE- TO BOARD WITHIN 10 DAYS- RETURN DEA CERTIFICATE, UNUSED DEA CII ORDER FORMS(DEA222) - TO DEA OFFICE  
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CLOSING PHARMACY   show
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show PHARMACEUTICAL CARE- PROMOTE HEALTH,PREVENT DISEASE,OPTIMIZE DRUG THERAPY, DRUG THERAPY PROBLEMS-IDENTFY,PREVENT,RESOLVE DRUG THERAPY PLAN-ASSESS ,EVALUATE,MONITOR,SUGGEST  
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PHARMACY OPERATIONS - RESPONSIBILITY   show
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PRACTICE FUNCTIONS, VERIFICATIONS   show
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show PHARMACY SUPPORT PERSON  
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show DISPLAY VIVBLE TO PUBLIC ORIGINAL LICENSE AND CERTIFICATES OF RENEWAL (COPY) ,BADGE=FIRST NAME,PHARMACIST  
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show PERMANENT LOG OF INITIALS OR ID CODES KEPT FOR MIN 2 YEARS, AVAIL FOR BOARD INSPECTIONS, FOR TEMPORARY STAFF-DATES AND SHIFTS WORKED ALSO. APPLIES TO RXT,INTERNS,TECHS,PSP  
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show REFRIGIRATION-WITH THERMOMETER SINK WITH HOT/COLD WATER LOCATED WITHING PHARMACY DEPARTMENT SECURE BARRIER IN ABSENCE OF RXT LIGHT,VENTILATION,TEMPERATURE, HUMIDITY- MAINTAINED TO PROPER STORE DRUGS ORDERLY AND CLEAN  
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BULK COUNTING MACHINES   show
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show NOTIFY BOARD AT LEAST 30 DAYS PRIOR TO COMMENCEMENT (APPLIES TO PREMISES CURRENTLY OCCUPIED OR INSTALLATION OF STERILE COMPOUNDING FACILITY) PRIOR OR DURING OR AT TEMPORARY LOCATION- ON SITE INSPECTION BY BOARD MAY BE REUIRED  
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show DIFENOXIN (LYSPAFEN) HEROIN(DIACETHYLMORPHIN) MARIJUANA LSD (LYSERGIC ACID DIETHYLAMIDE) PEYOTE DIHYDROMORPHINE MESCALINE  
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show ALPRAZOLAM(XANAX) STADOL,TORBUGESIC,TORBUTROL(BUTORPHANOL) CHLORALHYDRATE(NOCTEC) CLONAZEPAM(CLONOPIN) BARBITAL(BARBITONE) CHLORDIAZEPOXIDE(LIBRIUM,SK-LYGEN) DIAZEPAM(VALIUM, VALRELEASE) CLORAZEPATE(TRANXENE) REDUX(DEXFENFLURAMINE)  
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show PROPOXIFEN WITH OTHER INGREDIENTS:(DARVON,DALENE,PROPOCET,DARVOCET) DICHLORALPHENAZONE(MIDRIN) MOTOFEN(ATROPIN 25MCG/DIFENOXIN 1MG ESTAZOLAM(PROSOM, DOMNAMID,EURODIN,NUCTALON) ETHCHLORVYNOL(PLACIDYL) FENFLURAMINE(PONDIMIN,PONDERAL)  
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C-IV CONT   show
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C-IV CONT   show
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show ALFENTANIL(ALFENTA) AMOBARBITAL(AMYTAL,TUINAL) COCA LEAVES COCAINE AMPHETHAMINE(DEXEDRINE,BIPHETAMINE) CODEINE DEXTROPROPOXIPHENE,BULK NON DOSAGE FORM DIHYDROCODEINE(DIDRATE,PARZONE) DIPHENOXYLATE FENTANYL(SUBLIMAZE,DURAGEZIC,INNOVAR)  
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C-II CONT   show
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C-II CONT   show
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C-II CONT   show
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AMDS -AUTOMATED MEDICATION DISTRIBUTION SYSTEMS   show
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AUTOMATED PHARMACY SYSTEM   show
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show LOCATED IN THE PHARMACY  
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DECENTRALIZED AMDS   show
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OUTPATIENT AMDS   show
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show LICENSED PHARMACY STAFFED BY ONE OR MORE QUALIFIED CERTIFIED PHARMACY TECHNICIANS AT WHICH TELEPHARMACY SERVICES ARE PROVIDED THROUGH A LICENSED MANAGING PHARMACY  
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WHO IS IN CHARGE OF THE REMOTE SITE   show
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RESPONSIBILITIES OF PIC - AMDS   show
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show PIC  
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NOTIFICATION TO THE BOARD- RE: AMDS   show
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NOTICE TO THE BOARD RE AMDS SHOULD INCLUDE:   show
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show MANAGING PHARMACY - GENERAL PHARMACY LICENSE REMOTE DISPENSING SITE- LIMITED PHARMACY LICENSE (IT IS CONSIDERED AN EXTENSION OF MANAGING PHARMACY)  
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show NOT APPROVED IF WITHING SAME COMMUNITY OR 15 MILES OF MANAGING PHARMACY CONSIDER NEED FOR THIS SERVICE AND AVAILABILITY OF PHARMACISTS  
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INSPECTIONS OF AMDS   show
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HOW OFTEN TO TEST AMDS   show
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RANDOM VERIFICATION BY A PHARMACIST (DECENTRALIZED AMDS)   show
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show INCORRECT DRUG, DOSE, DOSAGE FORM ,OTHER ERRORS(INCLUDE DESCRIPTIONS)  
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CATEGORIES OR ERRORS IDENTIIED IN CENTRALIZED AMDS   show
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DO THESE AMDS ERRORS HAVE TO BE SUBMITTED TO THE BOARD?   show
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show IF THE AVERAGE ACCURACY DURING INITIAL 60 DAYS IS 99.7% FOR ALL DRUG DOSES DISPENSED  
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RANDOM VERIFICATION BY PHARMACIST (CENTRALIZED AMDS)   show
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IF AVERAGE ACCURACY OF AMDS IS NOT 99.7% FOR THE INITIAL 60 DAY PERIOD?   show
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show 1ST YEAR - QUARTERLY,AFTER 1 YEAR WHEN ACCURACY LESS THAN 99.7% WRITTEN REPORT INCLUDING CORRECTIVE ACTIONS  
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OUTPATIENT AMDS- VERIFICATION AND REPORTING   show
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REPORT ERRORS ID IN OUTPATIENT AMDS:   show
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show NO, ALL ORAL RX ORDERS SHOULD BE COMMUNICATED TO THE PHARMACIST  
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RX LABEL INFO FROM REMOTE SITE   show
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show LABEL AS SUCH: ATORVSTATIN, GENERIC FOR LIPITOR (BRAND)  
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show LABEL AS SUCH: LIPITOR FOR ATORVASTATIN  
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RECORDS AT REMOTE SITE -   show
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C-III   show
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show BUTABARBITAL( BUTISOL,BUTIBEL) BUTALBITAL(FIORINAL, BUTALBITAL WITH ASA) CODEINE AND ISOQUINOLINE ALCALOID (CODEINE WITH PAPAVERIN OR NOSCAPINE) CODEINE COMBINATION PRODUCTS (EMPIRIN, FIORINAL, TYLENOL ,ASA WITH CODEINE)  
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C-III CONT   show
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show NANDROLONE (DECABOLIN,DECA-DURABOLIN,DURABOLIN-50) METHYLTESTOSERONE (ANDROID,VIRILON,TESTRED,ORETON) NALORPHINE (NALLINE) NORETHANDROLONE(NILEVAR,SOLEVAR)  
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show OPIUM COMBINATION(PAREGORIC) PENTOBARBITAL AND NON CONTROLLED INGRIDIENTS PENTOBARBITAL SUPPOSITORY PHENDIMETRAZIL(BONTRIL) SECOBARBITAL WITH NON CONTROLLED SECOBARBITAL SUPPOSITORY TESTOSTERONE(ANDROID-T, ANDROLAN,DEPOTEST,DELATESTRYL)  
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show SEPARATE CS REGISTRATION REQUIRED FOR EACH LOCATION OF PRACTICE  
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DOCTOR WITH PRIVATE OFFICE WORKING AT A HOSPITAL- HOW MANY CS REGISTRATIONS?   show
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show CS C-I SHALL BE STORED IN SECURELY LOCKED SUBSTANTIALLY CONSTRUCTED CABINET CS C-II TO V MAY BE STORED IN SECURELY LOCKED SUBSTANTIALLY CONSTRUCTED CABINET OR MAY BE MIXED THROUGHOUT THE STOCK OF NONCONTROLLED SUBSTANCES TO OBSTRUCT THEFT OR DIVERSION  
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WHEN AND WHERE TO REPORT THEFT OR LOSS   show
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WHAT CAN BE ADDED BY A PHARMACIST TO CS RX?   show
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show PATIENT'S NAME CS PRESCRIBED (EXCEPT FOR GENERIC SUBSTITUTION NAME OR SIGNATURE OF PRESCRIBER  
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show DUE TO SHORT SUPPLY - WITHING 72 HOURS, AFTER 72 HRS- ONLY NEW RX FOR LTCF-OR TERMINALLY ILL- 60 DAYS  
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show IN MULTIPLE RX WITH START DATES FOR UP TO 90 DAYS  
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show PRESCRIBER CAN CALL OR FAX C-II RX PHARMACIST PREPARES WRITTEN OR PRINTED RECORD PHARMACIST RESPONSIBLE FOR VERIFYING PRESCRIBER IF NOT KNOWN DOCTOR RESPONSIBLE FOR PROVIDING WRITTEN SIGNED RX FOR EMERGENCY QTY TO BE DELIVERED TO PHARMACIST  
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show IMMEDIATE ADMIN REQUIRED NO APPROPRIATE ALTERNATIVE AVAILABLE PRESCRIBER UNABLE TO PROVIDE ELECTRONIC OR MANUALLY SIGNED WRITTEN RX  
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WHAT ADDITIONAL INFO WRITTEN ON THE FACE OF WRITTEN RX FOR EMERGENCY QTY?   show
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IF WRITTEN RX FOR EMERGENCY SUPPLY IS NOT DELIVERED WITHING 7 DAYS?   show
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CAN YOU REFILL C-II RX ?   show
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CAN YOU ALTER AUTHORIZED FILL DATES?   show
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HOW MANY MULTIPLE RXS FOR CONSECUTIVE FILLING ARE ALLOWED?   show
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CAN I FILL RX FAXED TO PHARMACY FOR C-III -V?   show
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show YES, BUT TOTAL QTY INCLUDING ORIGINAL RX SHOULD NOT EXCEED 6 MONTH SUPPLY AND NOT BE REFILLED MORE THAN 5 TIMES  
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show PHARMACIST OR INTERN UNDER SUPERVISION  
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show YES, BUT ONLY AFTER PHARMACIST FULFILLED PROFESSIONAL AND LEGAL RESPONSIBILITIES  
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WHEN SELLING C-V OTC ,RECORD WHAT?   show
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SELLING PSE,EPHEDRINE, PHENYLPROPANOLAMIE OTC - WHO CAN SELL AND HOW TO RECORD?   show
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WHAT PTS RECORD SHALL CONTAIN?   show
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WHAT ELSE IS REQUIRED IN THE PHARMACY CONCERNING SALE OF PSE,PPA,EPHE?   show
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INVENTORY OF C-II- HOW OFTEN AND HOW LONG TO KEEP RECORD OF?   show
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show PERPETUAL INVENTORY RECORD- MATCH ALL DRUGS RECIEVED WITH ALL RX FILLED - IF DISCREPANCY -NOTIFY PIC. PHYSICAL INVENTORY COUNT - ONCE A YEAR. RECORDS SHOULD MATCH/RECONCILED WITH PERPETUAL INVENTORY. MUST INCLUDE ID OF INDIVIDUAL PERFORMING INVENTORY  
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show BROWN+GREEN (SUPPLIER +DEA) -& BLUE(PURCHASER)  
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INVENTORY OF C-I AND C-II AND HYDROCODONE (SOLID ORAL,INJECTABLE )   show
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INVENTORY C-III,IV,V   show
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show 1.PREPARED ACCORDING TO LABELED INSTRUCT.EXPOSE TO POTENTIAL CONTAMIN. 2.CONTAINS NONSTERILE ING THAT MUST BE STERILIZED BEFORE ADMIN 3. BIOLOGIC,DIAGNOSTIC OR OTHER THAT REQ.TO BE STERILE WHEN ADMINISTERED  
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ANTE AREA   show
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ASEPTIC PROCEDURE   show
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BIOLOGICAL SAFETY CABINET   show
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show BASED ON RELIABLE LITERATURE SOURCES, MAINTAIN WRITTEN JUSTIFICATION OF STANDARDS OR, IF NOT AVAIL.-24 HOUR EXPIRY DATE  
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ADDITIONAL REFERENCE REQUIREMENT FOR COMPOUNDING STERILE PRODUCTS   show
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EXTRA PROCEDURE REQUIRED IN STERILE COMPOUNDING   show
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POLICIES AND PROCEDURES MANUAL   show
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show QUALITY ASSURANCE PROGRAM, SAMPLING, PREPARATION RECALL,HAZARDOUS PRODUCTS AND INFECTIOUS WASTE. HAS TO BE AVAILABLE FOR PERIODIC REVIEWS AND INSPECTION BY THE BOARD  
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LABEL REQUIREMENTS FOR STERILE PREPARTION   show
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show NAME AND QUANTITY OF ALL CONTENTS, INTERNAL CODE IDENTIFYING DATE AND TIME OF PREPARATION, AND UNIQUE ID OF PREPARER'S AND PHARMACIST'S, STABILITY,AUX LABELS  
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show ISO-5,3 OR LESS PRODUCTS,2 OR LESS ENTITIES(BAGS,VIALS) PREPARED BY OPENING AMPULE, PENETRATING STOPPER WITH STERILE NEEDLE AND TRANSFERRING TO ANOTHER FOR ADMIN.  
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STORAGE CONDITIONS FOR LOW RISK   show
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show MANUAL MEASURING AND MIXING 3 OR LESS MANUFACTURED PRODUCTS INCLUDING INF USION OR DILUTENT TO COMPOUND NUTRITIONAL SOLUTIONS  
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show ADMINISTRATION SHALL COMMENCE WITHING 12 HOURS OF THE START OF COMPOUNDING  
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show COMPOUNDED ASEPTICALLY UNDER LOW RISK CONDITIONS -MULTIPLE OR SMALL DOSES OF STERILE PRODUCTS ,MULTIPLE ADMINISTRATIONS OR MULTIPLE PATIENTS. COMPLEX ASEPTIC MANIPULATIONS, LONG PROCESS  
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show ROOM 30HOURS, COLD FOR 9 DAYS, SOLID FROZEN -25C FOR 45 DAYS  
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EXAMPLES OF MEDIUM RISK   show
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show PREPARATIONS THAT EITHER ARE CONTAMINATED OR AT RISK TO BE WHEN COMPOUNDED AND REQUIRES TERMINAL STERILIZATION  
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STORAGE CONDITIONS FOR HIGH RISK   show
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IMMEDIATE USE STERILE PREPARATIONS   show
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WHERE IMMEDIATE USE PREPARATIONS ARE UTILIZED?   show
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show VERTICAL FLOW CLASS II OR CLASS III BIOLOGICAL SAFETY CABINET (BSC) OR COMPOINDING SAFETY ISOLATOR (CAI)  
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POLICIES AND PROCEDURES FOR HAZ DRUGS PREP INCLUDE..   show
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PHARMACISTS VERIFICATION OF STERILE COMPOUNDS MUST INCLUDE..   show
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MEDIA-FILL TESTING BY PERSONNEL PERFORMED   show
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HOW OFTEN CLEAN ROOMS, LAMINAR AIRFLOW HOODS AND BARRIER ISOLATORS NEED TO BE CERTIFIED   show
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show AIR SAMPLING AND PRESSURE DIFFERENTIAL MONITORING  
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show LICENSED IN IOWA, MEET MIN STANDARDS OF TRAINING FOR MED USES OF RADIOACTIVE MATERIALS - SUBMIT AFFIDAVIT OF IT TO BOARD. COMPLETE 90 HRS COLLEGE TRAINING+160 hrs practical CLINICAL training .COMPLETE RESIDENCY.COMPLETE CERTIFICATE PROGRAM (ACPE)  
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show LICENSED IN IOWA, CERTIFIED BY BOARD OF PHARMACEUTICAL SPECIALTIES AS A BOARD CERTIFIED NUCLEAR PHARMACIST (BCNP) -SUBMIT AFFIDAVIT TO BOARD  
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show AT LEAST 25 FT SQUARE SEPARATE FROM NON RADIOACTIVE DRUGS FOR STORAGE AND PRODUCT DECAY  
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ADDITIONAL LABELS FOR INNER IMMEDIATE CONTAINER OF A RADIOACTIVE DRUG   show
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ADDITIONAL LABELS FOR OUTER CONTAINER   show
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show LAMINAR FLOW HOOD, DOSE CALIBRATOR, REFRIGERATOR, SINGLE CHANNEL SCINTILLATION COUNTER, MICROSCOPE, AUTOCLAVE,INCUBATOR ,RADIATION SURVEY METER.  
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IF A PHARMACISTS LICENSE IS SUSPENDED, SURRENDERED OR REVOKED ,WHEN CAN APPLICATION BE MADE TO REINSTATE   show
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WHAT IS REQUIRED TO REINSTATE LICENSE?   show
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show  
🗑
show  
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LABELING AND RECORDING OF POISONS   show
🗑
show  
🗑
show  
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DOCTOR WRITES RX FOR OTC PRODUCTS WITH DIFFERENT INSTRUCTIONS FROM THE BOX   show
🗑
show  
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IF OTC REPACKAGED - WHAT ARE LABELING REQUIREMENTS   show
🗑
show  
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INVESTIGATIONAL STATUS DRUGS - WHO CAN GIVE TO PATIENTS..   show
🗑
show  
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GENERAL PRACTITIONER WROTE RX FOR METHADONE FOR ADDICTION TREATMENT- IS IT ILLEGAL?   show
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I pass!!!!! no need to fill the rest:)):))   show
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Or sort by any of the columns using the down arrow next to any column heading.
If you know all the data on any row, you can temporarily remove it by tapping the trash can to the right of the row.

 
Embed Code - If you would like this activity on your web page, copy the script below and paste it into your web page.

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Created by: irina123
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