chap 4 Flashcards
The U.S. Food and Drug Administration regulates:
- Prescribing of drugs by MDs and NPs
- The official labeling for all prescription and over-the-counter drugs
- Off-label recommendations for prescribing
- Pharmaceutical educational offerings
- The official labeling for all prescription and over-the-counter drugs
The U.S. Food and Drug Administration approval is required for:
- Medical devices, including artificial joints
- Over-the-counter vitamins
- Herbal products, such as St John’s wort
- Medical devices, including artificial joints
An Investigational New Drug is filed with the U.S. Food and Drug Administration:
- When the manufacturer has completed phase III trials
- When a new drug is discovered
- Prior to animal testing of any new drug entity
- Prior to human testing of any new drug entity
- Prior to human testing of any new drug entity
Phase IV clinical trials in the United States are also known as:
- Human bioavailability trials
- Postmarketing research
- Human safety and efficacy studies
- The last stage of animal trials before the human trials begin
- Postmarketing research
Off-label prescribing is:
- Regulated by the U.S. Food and Drug Administration
- Illegal by NPs in all states (provinces)
- Legal if there is scientific evidence for the use
- Regulated by the Drug Enforcement Administration
- Legal if there is scientific evidence for the use
The U.S. Drug Enforcement Administration:
- Registers manufacturers and prescribers of controlled substances
- Regulates NP prescribing at the state level
- Sanctions providers who prescribe drugs off-label
- Provides prescribers with a number they can use for insurance billing
- Registers manufacturers and prescribers of controlled substances
Drugs that are designated Schedule II by the U.S. Drug Enforcement Administration:
- Are known teratogens during pregnancy
- May not be refilled; a new prescription must be written
- Have a low abuse potential
- May be dispensed without a prescription unless regulated by the state
- May not be refilled; a new prescription must be written
Precautions that should be taken when prescribing controlled substances include:
- Faxing the prescription for a Schedule II drug directly to the pharmacy
- Using tamper-proof paper for all prescriptions written for controlled drugs
- Keeping any pre-signed prescription pads in a locked drawer in the clinic
- Using only numbers to indicate the amount of drug to be prescribed
- Using tamper-proof paper for all prescriptions written for controlled drugs
Strategies prescribers can use to prevent misuse of controlled prescription drugs include:
- Use of chemical dependency screening tools
- Firm limit-setting regarding prescribing controlled substances
- Practicing “just say no” to deal with patients who are pushing the provider to prescribe controlled substances
- All of the above
- All of the above
Behaviors predictive of addiction to controlled substances include:
- Stealing or borrowing another patient’s drugs
- Requiring increasing doses of opiates for pain associated with malignancy
- Receiving refills of a Schedule II prescription on a regular basis
- Requesting that only their own primary care provider prescribe for them
- Stealing or borrowing another patient’s drugs
Medication agreements or “Pain Medication Contracts” are recommended to be used:
- Universally for all prescribing for chronic pain
- For patients who have repeated requests for pain medication
- When you suspect a patient is exhibiting drug-seeking behavior
- For patients with pain associated with malignancy
- Universally for all prescribing for chronic pain
A prescription needs to be written for:
- Legend drugs
- Most controlled drugs
- Medical devices
- All of the above
- All f the above