Lec 17 - Indiana Food, Drugs, and Cosmetics Flashcards
Written order for a drug or device for a patient in an inpatient institution
a. drug order
b. prescription
a. drug order
Written order for a drug or device for an outpatient
a. drug order
b. prescription
b. prescription
which of the following is NOT required on a drug order?
a. name and bed # of the patient
b. name and strength/size of the drug
c. amount to be dispense in quantity or days
d. written or electronic signature of practitioner
d. written or electronic signature of practitioner
(this is for prescriptions not drug orders)
which of the following is NOT needed on a prescription label?
a. Name, address, and phone number of the dispensing pharmacy
b. The name of the drug (trade or generic or both) in compliance with IC 16-42-22
c. Strength of the drug
d. The directions for use as provided in the prescription
e. For an animal, the owner’s name
c. Strength of the drug
required information for practitioner label (4)
- Directions for use of the drug
- Name and address of the practitioner
- Name of the patient
- If the drug is prescribed for an animal, the species of the animal
which of the following is NOT required on the practitioner label?
a. if for an animal, the owner’s name
b. directions for use of the drug
c. name of the patient
d. name and address of the practitioner
a. if for an animal, the owner’s name
(need the species, not owner’s name on practitioner label)
what does Indiana law say about anabolic steroids?
must be prescribed for a legitimate medical purpose, not for performance enhancing or hormonal manipulation not related to a medical necessity
mechanical storage devices can only be utilized in what 3 settings?
-Pharmacy that holds a permit issued by the Indiana BoP;
-Remote location under the jurisdiction of the Indiana BoP; or
-A licensed health care facility
T or F: designated Indiana BoP employees and all law enforcement officers in Indiana cannot make arrests without a warrant for suspected CS felony
F (they don’t need a warrant)
which of the following is TRUE about samples and coupons?
a. practitioners must ask for drug samples electronically
b. a drug sample is “a unit of a prescription drug that is intended to be sold”
c. community pharmacies cannot have drug samples at any time
d. starter packs are considered drug samples
c. community pharmacies cannot have drug samples at any time
(a. is in writing; b. is not intended for sale; d. is intended to be sold)
Two things Indiana specifies in addition to the PDMA
- You cannot remove a sample from its original packaging, repackage it, and then sell it/exchange it.
- You cannot deliver a drug sample to someone after its expiration date
we CANNOT substitute a generic for a brand name when a prescription is written by:
a. physicians
b. optometrists
c. veterinarians
d. podiatrists
e. dentists
f. APRNs
c. veterinarians
the “dispense as written” and “may substitute” lines are not required on _______ or _______ prescriptions
electronic; verbal
for Medicaid and CHIP patients, the pharmacist must substitute the product that results in lowest price unless: (2 things)
- “Brand medically necessary” is written or electronically transmitted in practitioner’s own handwriting; or
- Orally stating that a generic equivalent may not be substituted, and subsequently forwarding a covering prescription that has “Brand Medically Necessary” included
if a pharmacist substitutes a generic equivalent for a brand name, how would it be listed on the prescription label?
“_______ generic for _______”
(ex. lisinopril generic for zestril)
which book is used for biosimilar products substitution?
a. orange book
b. purple book
c. blue book
d. green book
b. purple book
biosimilar products can be substituted if it meets what 4 criteria?
- The product has been determined to be interchangeable by the FDA (purple book)
- The prescribing practitioner has indicated “may substitute”
- The pharmacist has informed the customer of the substitution
- After completing the substitution, the prescriber is informed of the name and manufacturer of the biologic product dispensed
which of the following is FALSE about a pharmacist or naloxone entity who dispenses the naloxone?
a. must register biannually with the state department or local health department
b. instruct the individual receiving the product to summon emergency services right away
c. provide education and training on drug overdose response and treatment
d. provide drug addiction treatment and referral information
a. must register biannually with the state department or local health department
(annually)
