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Pharm Tech Test 1

study guide for first test

QuestionAnswer
Provies incentives to promote research, approval, and marketing of drugs for rare diseases. Orphan Drug Act (1983)
Required pharmacists counsel Medicaid and Medicare patients on their medications Omnibus Budget Reconciliation Act (1990)
Protects consumers by reporting adverse drug reactions from these products Dietary Supplement and Nonprescription Drug Consumer Protection Act (2006)
Seperated drugs into two categories 1) Legend and 2) OTC Durham-Humphrey Amendment (1951)
Allows for both the extension of drug patent terms and quicker introduction of lower cost generic drugs Hatch-Waxman (1984)
Allows quicker approval of drugs needed for the treatment of life threatening conditions FDA Modernization Act (1997)
Prohibited False Claims about a drugs therapeutic effects Sherley Amendment (1911)
The purpose a drug is being used must be indicated on its labeling Alberty Food Products vs. US (1950)
Required the use of child proof packaging on prescription drugs Poison Prevention Packaging Act (1970)
acquired immunodeficiency syndrome AIDS
bowel movement BM
blood sugar BS
carcinoma CA
electrocardiogram EKG
as soon as possible ASAP
average wholesale price AWP
blood pressure BP
discontinue DC
Ethyl alcohol, ethynol EtOH
health maintenance organization HMO
isoniazid INH
keep vein open KVO
prescription drug legend
milliequivalent mEq
milk of magnesia MOM
nonsteroidal anti-inflammatory drug NSAID
nitroglycerin ntg
over the counter OTC
penicillin PCN
patient package insert PPI
temperature T
total parenteral nutrition TPN
NDC Section 1 identifies the drug manufacturer
NDC Section 2 Identifies the product name, strength, and dosage form
NDC Section 3 Identifies the package size
Parts of a Rx Label name, address and phone number of the pharmacy, name of the patient, prescription number, date of dispensing, expiration date, refills available, name strength and dosage form of medication, quantity of medication dispensed, directions for use
Drug Recall if drug causes severe adverse reaction or is improperly labeled by manufacturere, they are recalled
Drug Recall Class 1 exposure will cause severe health hazard or death
Drug Recall Class 2 exposure may cause temporary or medically reversible adverse health hazard
Drug Recall Class 3 exposure is not likely to cause an adverse health hazard
may be swallowed whole without chewing if a specific dose is required that isn't available as non-chewable tablet chewable tablet
the most popular dosage form available in various size, color, shape, and weight tablet
designed to be placed under tongue where the active ingredient is promptly absorbed into the blood stream sublingual tablet
must be shaken well before use and care must be given to affix a shake well auxillary label when dispensing suspension
frequently applied to oozing, weeping lesions because of their absorptive properties pastes
sweetened hydroalcoholic solutions and are probably most widely used. Popularity due to pleasant taste, relative stabliity and ease of preparation. Concentration of alcohol may vary but usually contains no more than 20% alcohol elixir
patches applied to the skin formulated to deliver a constant controlled dose of medication through the skin and into the blood stream. Sites of the application should be cleansed with alcohol and rotated transdermal patches
PHI Protected Health Information
3 examples of PHI name and address, SSN, payment history, medical history, account number, name and address of healthcare provider
Created by: LaurenH925
Popular Pharmacology sets

 

 



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