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!
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show | display original license and evidence of current renewal publicly
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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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show | person enrolled in a college of pharmacy, actively pursuing pharmacy degree,or registered with the board for the purpose of obtaining instructions in the practice of pharmacy from a preceptor (includes foreign graduate)
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Pharmacist - preceptor | show 🗑
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can a pharmacist serve as preceptor while the pharmacist's license is the subject of disciplinary sanction? | show 🗑
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Preceptor requirements (board of pharmacy rules, 657-4.9(155A) | show 🗑
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how many interns may preceptor supervise concurrently? | show 🗑
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Pharmacy technician- purpose of registration | show 🗑
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show | Iowa licensed pharmacist who is on duty in Iowa -licensed pharmacy and who is responsible for supervising the tech's actions
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how to register to be a pharmacy technician? | show 🗑
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show | still needs an application for registration as a trainee withing 30 days prior to training on-site (including college based or ashp program or tech training through work experience)
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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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After a prescription has been filled and dispensed, who is the legal owner of the prescription? | show 🗑
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For a drug to be considered Pharmaceutically Equivalent, all of the following must be true EXCEPT | show 🗑
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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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Which of these would be classified as Schedule III controlled substances? I. Anabolic Steroids II. Marinol III. Morphine | show 🗑
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show | program established by PIC who has determined that one or more certified pharmacy techs are qualified to safely check work of other certified tech and provide final verification for rx dispensed for subsequent admin to patient in institutional setting
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required hours for internships | show 🗑
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notifications to the Board : pharmacy | show 🗑
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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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written rx should contain: | show 🗑
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What additional items are required on a faxed prescription? | show 🗑
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show | Written signature of practitioner
Address of the practitioner
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show | 12 refills during 18 month (in practice- only 12 month)
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when can rx be refilled whithout authorization: | show 🗑
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show | CS III
BUTALBITAL WITH ASPIRIN
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PARTIAL FILL FOR CS II - I.E.MORPHINE FOR TERMINALLY ILL PATIENT | show 🗑
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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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• Does state have controlled substance(s) drugs of concern schedule differently than the Feds CSA? If so which drugs? | show 🗑
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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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Does state have a CS Rx PMP | show 🗑
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Marijuana schedule | show 🗑
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show | Dronabinol (Tetrahydrocannabinol (THC) )
C-III (state)
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show | C-V
Records must be kept for 2 years.
Effective in 2010, purchase records shall be recorded in the real‐time electronic pseudoephedrine tracking system (PTS) called the National Precursor Log Exchange (NPLEx).
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Ephedrine, phenylpropanolamine, pseudoephedrine LIMIT? | show 🗑
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Ephedrine, phenylpropanolamine, pseudoephedrine WHO can purchase? | show 🗑
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show | Pseudoephedrine exceeding the maximum 7500mg / 30 days may be dispensed for a legitimate medical purpose with a prescription
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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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Pentazocine, ZOLPIDEM(AMBIEN) ZOLEPON(SONATA) Phentermine Soma (Carisoprodol) BUTORPHNOL (STADOL) | show 🗑
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Lomotil (diphenoxylate w/ atropine) Promethazine/codeine elixir(PHENERGAN) | show 🗑
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show | permitted ONLY if the pharmacist receives the original written, signed prescription before actual dispensing
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Exceptions (fax = original) | show 🗑
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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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show | NURSE PRACTITIONER, ANESTHETIC SPECIALIST,MIDWIFE,PHYSICIAN ASSISTANT.
LICENSED OR REGISTERED OR PERMITTED TO PRESCRIBE CONTROLLED SUBSTANCES
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show | OPIUM 100MG/100ML (KAOLIN PECTATE PG, KAOPECTALIN PG, PAREPECTOLIN)
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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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show |
PURCHASER SHOULD BE AT LEAST 18 YEARS OLD
OPIUM 240 ML/48 DOSAGE UNITS
OTHER C-V 120ML/24DOSAGE UNITS
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MAX AMOUNT OF CODEINE ALLOWED FOR SALE OTC IN 48HRS | show 🗑
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show | C-II
IF 0.5MG/ML-CS-III
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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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CISPLATIN COMPOUNDED UNDER: | show 🗑
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DEA 363 | show 🗑
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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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WHAT IS REPORTABLE UNDER CQI | show 🗑
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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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show | FILED CHRONOLOGICALLY BY DATE OF DISCOVERY
EVENTS SHALL BE DOCUMENTED AS SOON AS PRACTICABLE AND INCLUDE DESCRIPTION OF THE EVENT, DATE AND TIME OF DISCOVERY ,NAME OF STAFF PERSON THAT DISCOVERED EVENT
NAME OF ALL INDIVIDUALS RECORDING AND REVIEWING
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VACCINE ADMINISTRATION BY PHARMACISTS | show 🗑
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WHAT ARE THE REQUIREMENTS FOR VACCINE ADMINISTRATION | show 🗑
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OTHER REQUIREMENTS FOR VACCINE ADMINISTRATION | show 🗑
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show | NOTIFY PRESCRIBER WHO SIGNED PROTOCOL WITHIN 24 HOURS OF EVENT AND SUBMIT REPORT TO VAERS
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show | Pharmacy SHALL NOT execute sale or closing unless there is adequate time to notify :
PIC OF CLOSING PHARMACY(40DAYS) ,BOARD AND DEA (30DAYS),PATIENTS (30DS),PIC OF RECEIVING PHARMACY(30DS)
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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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CLOSING PHARMACY-RECORDS | show 🗑
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CLOSING PHARMACY - RETURN WHAT AND WHEN | show 🗑
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CLOSING PHARMACY | show 🗑
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UNIVERSAL PRACTICE STANDARTS | show 🗑
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show | THE PHARMACY AND PIC RESPONSIBLE FOR COMPLIANCE WITH FEDERAL AND STATE LAWS,RULES,REGULATIONS RELATING TO PHARMACY PRACTICE ND OPERATIONS
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PRACTICE FUNCTIONS, VERIFICATIONS | show 🗑
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show | PHARMACY SUPPORT PERSON
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PHARMACIST ID | show 🗑
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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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C-IV | show 🗑
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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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show | LORAZEPAM(ATIVAN)
FLURAZEPAM(DALMANE)
MIDAZOLAM(VERSED)
PEMOLINE(CYLERT)
MAZINDOL(SANOREX,MAZANOR)
MEPROBAMATE(MILTOWN,EQUANIL,
DEPROL,EQUAGESIC, MEPROSPAN)
PENTAZOCIN(TALWIN,TALWINNX,
TALWIN COMPOUND, TALACEN)
MODAFINIL(PROVIGIL,ALERTEC)
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show | OXAZEPAM(SERAX,SERENID-D)
PRAZEPAM(CENTRAX)
PHENOBARBITAL(LUMINAL,DONNATAL,
BELLERGAL-S)
PHENTERMIN(IONAMIN,FASTIN,ADIPEX-P,
OBE-NIX,ZANTRYL)
QUAZEPAM(DORAL,DORMALIN)
HALCION(TRIAZOLAM)
SIBUTRAMIN(MERIDIA)
TEMAZEPAM(RESTORIL)
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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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show | LONG ACTING METHADONE (LAAM,LEVO-ALPHACETYLMETHADOL,
LEVO-METHADYLACETATE)
METHADONE(METHADOSE,DOLOFIN,AMIDONE)
METHYLPHENIDATE(RITALIN)
MORPHINE(STATEX,MSCONTIN,ROXANOL,
DURAMORPH,RMS,MSIR)
OXYCODONE(OXYCONTINE,TYLOX,PERCOCET,
ROXYCODONE,ROXYCET)
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show | OPIUM(POPPY,RAW,TINCTURE,GRANULATED,POWDERED)
METHAMPHETAMINE(SPEED,CRANK,DESOXYNE,ICE, D-DESOXYEPHEDRINE)
POPPY STRAW CONCENTRATE
OXYMORPHONE(NYMORPHAN)
REMIFENTANIL(ULTIVA)
SUFENTANIL(SUFENTA)
PENTOBARBITAL(NEMBUTAL)
SECOBARBITAL(SECONAL)
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AMDS -AUTOMATED MEDICATION DISTRIBUTION SYSTEMS | show 🗑
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show | USES AMDS TO MONITOR AND CONTROL DISPENSING, AND PROVIDES FOR DUR AND COUNSELING VIA ELECTRONIC METHOD BETWEEN PHARMACY AND REMOTE DISPENSING SITE
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CENTRALIZED AMDS | show 🗑
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show | LOCATED WITHING INSTITUTION WHERE DRUGS ARE DISPENSED BUT OUTSIDE OF PHARMACY DEPARTMENT
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OUTPATIENT AMDS | show 🗑
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REMOTE DISPENSING SITE | show 🗑
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show | PIC OF MANAGING PHARMACY =PIC OF THE REMOTE SITE
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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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show | NAME,ADDRESS,LICENSE OF THE PHARMACY
LOCATION OF AMDS
ID OF PIC
NAME,MANUFACTURER,MODEL OF SYSTEM
DESCRIPTION OF CHANGE OR UPGRADE AND INTENDED USE OF THE AMDS
COPY OF THE QUALITY ASSURANCE PLAN
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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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show | MONTHLY INSPECTIONS, REPORTS TO BE AVAILABLE TO THE BOARD FOR A MIN OF 12 MONTH FROM DATE OF INSPECTION
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show | MIN EVERY 6 MONTH -DOCUMENT TESTING OF EACH SYSTEM, INCLUDING ELECTRONIC AUDIO VIDEO COMMINICATIONS COMPONENTS
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RANDOM VERIFICATION BY A PHARMACIST (DECENTRALIZED AMDS) | show 🗑
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CATEGORIES OF ERRORS IDENTIFIED IN DECENTRALIZED AMDS | show 🗑
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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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show | 5% OF ALL DRUG DOSES DISPENSED DAILY BY AMDS VERIFIED BY PHARMACIST
OR
100% OF ALL DRUG DOSES DISPENSED ON A SPECIFIC DAY EACH MONTH TO BE VERIFIED BY PHARMACIST
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show | 100% OF DRUG DOSES SHALL BE VERIFIED UNTIL 99.7% ACHIEVED FOR 60 CONSECUTIVE DAYS
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REPORTING OF ERRORS TO THE BOARD | show 🗑
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OUTPATIENT AMDS- VERIFICATION AND REPORTING | show 🗑
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show | INCORRECT DRUG,QUANTITY,DOSE,DOSAGE FORM, DIRECTIONS FOR USE,PATIENT NAME,OTHER LABEL INFO,COMPUTER ORDER ENTRY ERROR,OTHER (DESCRIBE)
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CAN A PHARMACY TECH AT REMOTE LOCATION RECIEVE ORAL RX ORDERS FROM PHYSICIANS? | show 🗑
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RX LABEL INFO FROM REMOTE SITE | show 🗑
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IF GENERIC SELECTED FOR BRAND- | show 🗑
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BRAND SELECTED FOR GENERIC PRESCRIBED | show 🗑
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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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show | DRONABINOL IN SOFT GELATIN CAPS IN SESAME OIL (MARINOL)
HYDROCODONE AND ISOQUINOLINE ALCALOID
HYDROCODONE COMBINATION PRODUCTS (TUSSIONEX,VICODIN,LORTAB,HYCODAN, ANEXSIA,TUSSEND)
LYSERGIC ACID AND LYSERGIC ACID AMIDE
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C-III CONT | show 🗑
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C-III CONT | show 🗑
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show | SEPARATE CS REGISTRATION REQUIRED FOR EACH LOCATION OF PRACTICE
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show | ONE FOR OFFICE LOCATION- PRESCRIBER IS NOT REQUIRED TO MAINTAIN SEPARATE CS REGISTRATION FOR HOSPITAL
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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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show | PATIENT'S ADDRESS (WITH VERIFICATION)
AFTER CONSULTING WITH DR- PHARMACIST MAY CHANGE:
DRUG STRENGTH
DOSAGE FORM
DRUG QTY
DIRECTIONS FOR USE
DATE THE RX WAS ISSUED
DR'S ADDRESS OR DEA REGISTRATION NUMBER
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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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show | "AUTHORIZATION FOR EMERGENCY DISPENSING"
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show | PHARMACIST SHALL NOTIFY THE BOARD AND THE DEA
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show | NO - ONLY MULTIPLE RXS WITH AUTHORIZED START DATES FOR MAX 90DAYS TOTAL
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show | NO -THE PHARMACIST SHALL NOT CONTACT THE PRESCRIBER FOR VERBAL AUTHORIZATION PRIOR TO DATE WRITTEN
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HOW MANY MULTIPLE RXS FOR CONSECUTIVE FILLING ARE ALLOWED? | show 🗑
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show | YES. WITHING 6 MONTH OF ISSUE AND NOT MORE THAN 5 TIMES
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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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WHO MAY DISPENSE OTC C-V ? | show 🗑
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CAN A CASHIER COMPLETE SALE OF C-V? | show 🗑
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show | IN THE BOUND RECORD BOOK WITH PAGES SEWN OR GLUED TO THE SPINE, RECORD
NAME/ADDRESS -PURCHASER
NAME AND ID OF SELLING PHARMACIST/INTERN
NAME/QTY OF C-V PURCHASED/
DATE OF PURCHASE
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SELLING PSE,EPHEDRINE, PHENYLPROPANOLAMIE OTC - WHO CAN SELL AND HOW TO RECORD? | show 🗑
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show | NAME,ADDRESS,SIGNATURE OF PURCHASER
PRODUCT:NAME/QTY-TOTAL MGS OF E,PSE,PPA
DATE/TIME
RPH/INTERN-ID
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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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COLORS OF DEA 222 | show 🗑
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INVENTORY OF C-I AND C-II AND HYDROCODONE (SOLID ORAL,INJECTABLE ) | show 🗑
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show | QTY COULD BE ESTIMATED , EXCEPT FOR HYDROCODONE SOLID ORAL AND INJECTABLE-EXACT COUNT
IF BOTTLE OPENED : >100 - EXACT COUNT
LIQUID ORAL HYDROCODONE CONTAINING PRODUCTS-MEASURED TO NEAREST INCREMENT OR ESTIMATE TO NEAREST QUARTER
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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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show | ISO CLASS 8 OR SUPERIOR AREA WHERE PREPARATIONS ARE MADE (INCLUD.LABEL GENERATING ,PERSONNEL HYGIENE ,ORDER ENTRY
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|
||||
show | METHOD THAT INVOLVES SEPARATE STERILIZATION OF PRODUCT AND PACKAGE,TRANSFER INTO AND CLOSURE OF CONTAINER UNDER AT LEAST ISO 5 CONDITIONS USING PROCEDURES TO PRECLUDE CONTAMININATION BY MICROORG DURING PROCESSING
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|
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BIOLOGICAL SAFETY CABINET | show 🗑
|
||||
show | BASED ON RELIABLE LITERATURE SOURCES, MAINTAIN WRITTEN JUSTIFICATION OF STANDARDS OR, IF NOT AVAIL.-24 HOUR EXPIRY DATE
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|
||||
show | 1.CURRENT REFERENCE RELATED TO STERILE PRODUCTS AND PREPARATIONS
2. GENERAL INFO REFERENCE
3. INJECTABLE DRUG COMPATABILITY REF
4. REFERENCE RELATED TO HAZARDOUS DRUGS
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|
||||
EXTRA PROCEDURE REQUIRED IN STERILE COMPOUNDING | show 🗑
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||||
show | WRITTEN POLICY AND PROCEDURES MANUAL
SHALL BE PREPARED, IMPLEMENTED,
MAINTAINED AND ADHERED TO
FOR COMPOUNDNG, DISPENSING,
DELIVERY,ADMINISTRATION,STORAGE,
AND USE OF STERILE PREPARATIONS.
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|
||||
WHAT IS INCLUDED IN POLIC AND PROC MANUAL? | show 🗑
|
||||
LABEL REQUIREMENTS FOR STERILE PREPARTION | show 🗑
|
||||
IF STERILE PRODUCT PREPARED AS BATCH -WHAT IS REQUIRED | show 🗑
|
||||
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 🗑
|
||||
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
🗑
|
||||
STORAGE CONDITIONS FOR MEDIUM RISK | show 🗑
|
||||
show | TPN FLUIDS, 3 OR MORE AMPULES OR VIALS INTO ONE FINAL STERILE CONTAINER, INFUSION DEVICES
🗑
|
||||
show | PREPARATIONS THAT EITHER ARE CONTAMINATED OR AT RISK TO BE WHEN COMPOUNDED AND REQUIRES TERMINAL STERILIZATION
🗑
|
||||
STORAGE CONDITIONS FOR HIGH RISK | show 🗑
|
||||
IMMEDIATE USE STERILE PREPARATIONS | show 🗑
|
||||
WHERE IMMEDIATE USE PREPARATIONS ARE UTILIZED? | show 🗑
|
||||
HOW HAZARDOUS DRUGS SHOULD BE COMPOUNDED? | show 🗑
|
||||
show | STORAGE AND HANDLING,
CAUTION LABELING,PREP AREA,
PROTECTIVE APPAREL,
TECHNIQUES,TRAINING,
WASTE,SPILLS
🗑
|
||||
show | VISUAL INSPECTION OF LABELING,PHYSICAL INTEGRITY, EXPECTED APPEARANCE,FINAL FILL AMOUNT
🗑
|
||||
MEDIA-FILL TESTING BY PERSONNEL PERFORMED | show 🗑
|
||||
show | EVERY 6 MONTH AND WHEN DEVICE IS RELOCATED
🗑
|
||||
show | AIR SAMPLING AND PRESSURE DIFFERENTIAL MONITORING
🗑
|
||||
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)
🗑
|
||||
show | LICENSED IN IOWA, CERTIFIED BY BOARD OF PHARMACEUTICAL SPECIALTIES AS A BOARD CERTIFIED NUCLEAR PHARMACIST (BCNP) -SUBMIT AFFIDAVIT TO BOARD
🗑
|
||||
WHAT ADDITIONAL AREA REQUIRED FOR NUCLEAR PHARMACY | show 🗑
|
||||
ADDITIONAL LABELS FOR INNER IMMEDIATE CONTAINER OF A RADIOACTIVE DRUG | show 🗑
|
||||
show | NAME OF RADIONICLIDE,CHEMICAL FORM,AMOUNT OF RADIOACTIVE MATERIAL CONTAINED IN MLLI OR MICROCURIES,IF LIQUID - VOLUME IN CUBIC CM,REQUESTED CALIBRATION TIME FOR THE AMOUNT CONTAINED
🗑
|
||||
show | LAMINAR FLOW HOOD,
DOSE CALIBRATOR,
REFRIGERATOR,
SINGLE CHANNEL SCINTILLATION
COUNTER,
MICROSCOPE,
AUTOCLAVE,INCUBATOR
,RADIATION SURVEY METER.
🗑
|
||||
IF A PHARMACISTS LICENSE IS SUSPENDED, SURRENDERED OR REVOKED ,WHEN CAN APPLICATION BE MADE TO REINSTATE | show 🗑
|
||||
show | NABP EXAMS - NAPLEX AND IOWA MPJE
🗑
|
||||
show |
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|
||||
show |
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|
||||
show |
🗑
|
||||
PATIENT ASK FOR LOMOTIL - | show 🗑
|
||||
show |
🗑
|
||||
show |
🗑
|
||||
REPACKAGING OF OTC - ALLOWED IN THE REGULAR PHARMACY? | show 🗑
|
||||
show |
🗑
|
||||
LEGEND DRUGS - IF SUBSTITUTION ALLOWED BY DOCTOR, CAN BE FILLED WITH; CHEMICALLY IDENTICAL, PHARMACEUTICALY IDENTICAL, PHARMACOLOGICALY IDENTICAL OR AS PRESCRIBED | show 🗑
|
||||
INVESTIGATIONAL STATUS DRUGS - WHO CAN GIVE TO PATIENTS.. | show 🗑
|
||||
FORGED RX REPORTED, INVESTIGATION STARTED, WHO CAN PHARMACIST ALLOW TO SEE ORIGINAL RX | show 🗑
|
||||
GENERAL PRACTITIONER WROTE RX FOR METHADONE FOR ADDICTION TREATMENT- IS IT ILLEGAL? | show 🗑
|
||||
I pass!!!!! no need to fill the rest:)):)) | show 🗑
|
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