Kaduceus CW101- Unit 2 | PT 2
There are three classes of recalls:
Class 1 (CI): products that could cause serious harm or prove fatal
Class 2 (CII): products found to cause a temporary health problem
or pose a slight threat of serious harm
Class 3 (CIII): products that may have a minor defect or other
condition that would not harm the patient
Commonly known as narcotics, controlled substances are addictive.
They are derived from opium or opium-like substances. Opium comes
from the poppy seed plant and has analgesic effects that also affect
mood and behavior.
Some examples of substances created from opium
are codeine and morphine
Each type of narcotic is assigned a rating that depends on its
addictive and abuse potential.
There are five levels based on potential for abuse:
CI - Strongest potential for abuse; no medicinal use in the USA.
Examples: Marijuana, LSD, Heroine, Peyote, Methamphetamine
CII - Must be locked up because of high potential for abuse.
Examples: Cocaine, Ritalin, several amphetamines, dilaudid
CIII - Has abuse potential, but not like schedule II.
Examples: Combinations of hydrocodone and codeine products
CIV - Low potential for abuse.
Examples: Valium (diazepam), halcion (triazolam)
CV - Has the lowest abuse potential. Consists of preparation with
very limited amounts of controlled substance in each dose. It is kept
OTC in some states because of low potential abuse.
Examples: Lamotil and some cough syrups containing codeine
The U.S. Attorney assigns the schedule for a drug. Individual states
cannot establish the schedule under which a drug should be placed.
New scripts have up to eight different tamper-proof
security marks on them.
Prevents forgery and fraud
REMS: Risk Evaluation and Mitigation Strategy
No special prescribing requirement exists for Heroin
The DEA has three main registration forms:
Form 224: Dispensing controlled substances
Form 225: Manufacturing or distributing controlled substances
Form 363: To run a narcotic treatment program or compound narcotics
Form 222: Used for the purchasing and returning of outdated CII drugs
Form 41: Return to reverse distributor damaged, outdated or
unwanted controlled substances
Strict guidelines include:
Drugs rated CIII through CV can be refilled a maximum of five times
or within 6 months of the original order, whichever comes first
Records must be kept with the pharmacist’s initials and
the date the drug was dispensed
Pharmacies must physically cont schedule II drugs every two years
The Controlled Substance Act requires pharmacies to purchase
class-II controlled substances with DEA form 222. The pharmacy
obtains CII substances from a distributor and only one item may
be ordered per line when using DEA form 222.
Copy 1 and 2 are sent to the supplier
Copy 1: (original, brown) Retained by the supplier
Copy 2: (first carbon copy, green) Forwarded to the DEA
Copy 3: (second carbon copy, blue) Stays with the pharmacist (purchaser)
DEA Form 222 must be filled out with pen, typewriter, or an indelible
pencil and can be signed by the pharmacist who signed Form 224 or
the person who has been the legally designated Power of Attorney by
that pharmacist. Drugs must be checked in and an invoice stapled to
the completed DEA-222. Filing electronically is only possible for CV - CIII.
Pharmacy retains bottom copy
Invoices and forms must be kept onsite and made readily available
for inspection for 2 years. It is recommended that records of
invoices and forms are kept for 5 years.
Perpetual inventory. The pharmacist must validate all counts done by a
technician. Discrepancies are investigated by the DEA. Controlled
substance inventory must be performed every 2 years.
All controlled substances that are unwanted, unusable, or outdated
that are returned to the distributor. It prevents drug diversion, or the
intentional misuse of a drug intended for medical purposes or
recreational use of a prescription or a scheduled drug.
Original fill of CII through CV:
Written, oral, or fax
Emergency CII original fill:
Verbal order only in emergency situations
Refills of CII through CV:
CII - No refills
CIII and CIV - 5 times within 6 months
CV - No restrictions
CIII, CIV, and CV must have the remainder dispensed within 6 months.
CII must have remainder dispensed within 72 hours.
Transfer of prescriptions CII through CV may be transferred only
once. Write void on invalid prescription to inform that prescriptions
have been transferred.
Some states require Schedule V drugs to be dispensed by a pharmacist.
Controlled substances CII through CV may be mailed as long as the
contents are not identified on the packaging.
Contained in the Physician’s Desk Reference (PDR) in the doctor’s
office and Facts and Comparisons in the pharmacy.
Includes: Description, clinical pharmacology, indications and usage,
contraindications, warnings, precautions, drug abuse and dependence,
adverse reactions, dosage, and how its supplied. Box Warning is
also called Black Box Warning.
MedGuides: Printouts required for certain medications.
FDA established five categories to identify a drug’s potential harm
to a fetus or pregnant woman.
Category X - Not to be used during pregnancy.
Can produce the highest degree of teratogenicity.
Category A - No evidence of harm based on studies.
Category B-D - Various levels of risk.
Who can prescribe? The FDA and DEA have no
authority to determine prescribers.
Prescribers are licensed by their individual state board
Standard practitioners in all 50 states are physicians,
surgeons, doctors of osteopathy, dentists, podiatrists,
veterinarians, and optometrists
Pharmacy technicians take in prescriptions, interpret them and
fill them. Technicians cannot take phone orders. Pharmacists give
the final check and take verbal telephone orders and transfer
prescriptions to another pharmacy.
The information on a prescription label differs from a prescription
order. Two necessary components are pharmacy information
and patient information.
Special labeling sometimes is required because of adverse
effects or the possibility of teratogenicity to an unborn fetus.
Labels Include: Name, address, and phone number of the
pharmacy, name of prescriber and date prescription was filled;
prescription number and precautions.
License or DEA number of the prescriber is only required for a CII drug.
Medication taken from bulk packages and placed into blister
packs or unit-dosing devices must include:
Drug name
Strength and dosage form
Manufacturing and lot number
Expiration date
All prescribers must be registered with the DEA to write prescriptions
for controlled substances. Prescribers are given a nine-character
identification code, which is different for each prescriber.
The first two characters will be the letter A, B, F, or M, followed by
the first letter of the prescriber’s last name.
If the first character begins with the identifier P or R, they are typically
from a manufacturer, distributor, researcher, analytical lab, importer,
exporter, reverse distributor, or a narcotic treatment program.
The next seven digits are composed of numbers added together.
All prescription orders for controlled substances must be verified for authenticity
by the pharmacist. Confirmation of a prescriber’s DEA number may aid in verifying
the authenticity of a controlled substance prescription order.
Verifying a DEA Number:
Add the 1st, 3rd, and 5th digits together. (SUM 1)
Add the 2nd, 4th, and 6th digits together, then multiply by two. (SUM 2)
Add SUM 1 and SUM 2 together. (SUM 3)
The last digit of SUM 3 should match the 7th digit of the given DEA number.
Example Number: AP5836727
5 + 3 + 7 = 15
8 + 6 + 2 = 16 x 2 = 32
15 + 32 = 47
AP583672**7** = 4**7** ✓
Programs for opioid maintenance:
Methadone Maintenance Treatment (MMT)
Suboxone and Subtex
Risk management programs for prescription drugs:
iPledge Program
MSDS is a U.S. government-managed entity that oversees safety in
the workplace. Safety Data Sheets must be available for all chemicals.
Includes information on storage requirements, handling, and what
to do in case of a spill or contact with the eyes.
Their mission is to improve the safety and quality of care via the
accreditation of healthcare organizations. Areas of concern:
How look-alike and sound-alike drugs are identified
How communication, allergy notification, conflicting prescriptions.
verbal orders, and other areas that may create an avenue for errors handled
State Law: differs by state
Liabilities include: negligence or tort
Mistakes are made for many reasons
Consider purchasing malpractice insurance
Laws change regularly
There are three classes of recalls:
Class 1 (CI): products that could cause serious harm or prove fatal
Class 2 (CII): products found to cause a temporary health problem
or pose a slight threat of serious harm
Class 3 (CIII): products that may have a minor defect or other
condition that would not harm the patient
Commonly known as narcotics, controlled substances are addictive.
They are derived from opium or opium-like substances. Opium comes
from the poppy seed plant and has analgesic effects that also affect
mood and behavior.
Some examples of substances created from opium
are codeine and morphine
Each type of narcotic is assigned a rating that depends on its
addictive and abuse potential.
There are five levels based on potential for abuse:
CI - Strongest potential for abuse; no medicinal use in the USA.
Examples: Marijuana, LSD, Heroine, Peyote, Methamphetamine
CII - Must be locked up because of high potential for abuse.
Examples: Cocaine, Ritalin, several amphetamines, dilaudid
CIII - Has abuse potential, but not like schedule II.
Examples: Combinations of hydrocodone and codeine products
CIV - Low potential for abuse.
Examples: Valium (diazepam), halcion (triazolam)
CV - Has the lowest abuse potential. Consists of preparation with
very limited amounts of controlled substance in each dose. It is kept
OTC in some states because of low potential abuse.
Examples: Lamotil and some cough syrups containing codeine
The U.S. Attorney assigns the schedule for a drug. Individual states
cannot establish the schedule under which a drug should be placed.
New scripts have up to eight different tamper-proof
security marks on them.
Prevents forgery and fraud
REMS: Risk Evaluation and Mitigation Strategy
No special prescribing requirement exists for Heroin
The DEA has three main registration forms:
Form 224: Dispensing controlled substances
Form 225: Manufacturing or distributing controlled substances
Form 363: To run a narcotic treatment program or compound narcotics
Form 222: Used for the purchasing and returning of outdated CII drugs
Form 41: Return to reverse distributor damaged, outdated or
unwanted controlled substances
Strict guidelines include:
Drugs rated CIII through CV can be refilled a maximum of five times
or within 6 months of the original order, whichever comes first
Records must be kept with the pharmacist’s initials and
the date the drug was dispensed
Pharmacies must physically cont schedule II drugs every two years
The Controlled Substance Act requires pharmacies to purchase
class-II controlled substances with DEA form 222. The pharmacy
obtains CII substances from a distributor and only one item may
be ordered per line when using DEA form 222.
Copy 1 and 2 are sent to the supplier
Copy 1: (original, brown) Retained by the supplier
Copy 2: (first carbon copy, green) Forwarded to the DEA
Copy 3: (second carbon copy, blue) Stays with the pharmacist (purchaser)
DEA Form 222 must be filled out with pen, typewriter, or an indelible
pencil and can be signed by the pharmacist who signed Form 224 or
the person who has been the legally designated Power of Attorney by
that pharmacist. Drugs must be checked in and an invoice stapled to
the completed DEA-222. Filing electronically is only possible for CV - CIII.
Pharmacy retains bottom copy
Invoices and forms must be kept onsite and made readily available
for inspection for 2 years. It is recommended that records of
invoices and forms are kept for 5 years.
Perpetual inventory. The pharmacist must validate all counts done by a
technician. Discrepancies are investigated by the DEA. Controlled
substance inventory must be performed every 2 years.
All controlled substances that are unwanted, unusable, or outdated
that are returned to the distributor. It prevents drug diversion, or the
intentional misuse of a drug intended for medical purposes or
recreational use of a prescription or a scheduled drug.
Original fill of CII through CV:
Written, oral, or fax
Emergency CII original fill:
Verbal order only in emergency situations
Refills of CII through CV:
CII - No refills
CIII and CIV - 5 times within 6 months
CV - No restrictions
CIII, CIV, and CV must have the remainder dispensed within 6 months.
CII must have remainder dispensed within 72 hours.
Transfer of prescriptions CII through CV may be transferred only
once. Write void on invalid prescription to inform that prescriptions
have been transferred.
Some states require Schedule V drugs to be dispensed by a pharmacist.
Controlled substances CII through CV may be mailed as long as the
contents are not identified on the packaging.
Contained in the Physician’s Desk Reference (PDR) in the doctor’s
office and Facts and Comparisons in the pharmacy.
Includes: Description, clinical pharmacology, indications and usage,
contraindications, warnings, precautions, drug abuse and dependence,
adverse reactions, dosage, and how its supplied. Box Warning is
also called Black Box Warning.
MedGuides: Printouts required for certain medications.
FDA established five categories to identify a drug’s potential harm
to a fetus or pregnant woman.
Category X - Not to be used during pregnancy.
Can produce the highest degree of teratogenicity.
Category A - No evidence of harm based on studies.
Category B-D - Various levels of risk.
Who can prescribe? The FDA and DEA have no
authority to determine prescribers.
Prescribers are licensed by their individual state board
Standard practitioners in all 50 states are physicians,
surgeons, doctors of osteopathy, dentists, podiatrists,
veterinarians, and optometrists
Pharmacy technicians take in prescriptions, interpret them and
fill them. Technicians cannot take phone orders. Pharmacists give
the final check and take verbal telephone orders and transfer
prescriptions to another pharmacy.
The information on a prescription label differs from a prescription
order. Two necessary components are pharmacy information
and patient information.
Special labeling sometimes is required because of adverse
effects or the possibility of teratogenicity to an unborn fetus.
Labels Include: Name, address, and phone number of the
pharmacy, name of prescriber and date prescription was filled;
prescription number and precautions.
License or DEA number of the prescriber is only required for a CII drug.
Medication taken from bulk packages and placed into blister
packs or unit-dosing devices must include:
Drug name
Strength and dosage form
Manufacturing and lot number
Expiration date
All prescribers must be registered with the DEA to write prescriptions
for controlled substances. Prescribers are given a nine-character
identification code, which is different for each prescriber.
The first two characters will be the letter A, B, F, or M, followed by
the first letter of the prescriber’s last name.
If the first character begins with the identifier P or R, they are typically
from a manufacturer, distributor, researcher, analytical lab, importer,
exporter, reverse distributor, or a narcotic treatment program.
The next seven digits are composed of numbers added together.
All prescription orders for controlled substances must be verified for authenticity
by the pharmacist. Confirmation of a prescriber’s DEA number may aid in verifying
the authenticity of a controlled substance prescription order.
Verifying a DEA Number:
Add the 1st, 3rd, and 5th digits together. (SUM 1)
Add the 2nd, 4th, and 6th digits together, then multiply by two. (SUM 2)
Add SUM 1 and SUM 2 together. (SUM 3)
The last digit of SUM 3 should match the 7th digit of the given DEA number.
Example Number: AP5836727
5 + 3 + 7 = 15
8 + 6 + 2 = 16 x 2 = 32
15 + 32 = 47
AP583672**7** = 4**7** ✓
Programs for opioid maintenance:
Methadone Maintenance Treatment (MMT)
Suboxone and Subtex
Risk management programs for prescription drugs:
iPledge Program
MSDS is a U.S. government-managed entity that oversees safety in
the workplace. Safety Data Sheets must be available for all chemicals.
Includes information on storage requirements, handling, and what
to do in case of a spill or contact with the eyes.
Their mission is to improve the safety and quality of care via the
accreditation of healthcare organizations. Areas of concern:
How look-alike and sound-alike drugs are identified
How communication, allergy notification, conflicting prescriptions.
verbal orders, and other areas that may create an avenue for errors handled
State Law: differs by state
Liabilities include: negligence or tort
Mistakes are made for many reasons
Consider purchasing malpractice insurance
Laws change regularly