E01_02 Drug Interactions and Pharmacovigilance Flashcards
2017, 2018_Drug Interactions and Pharmacovigilance
The scope of pharmacovigilance covers the following areas of adverse effects of drugs except?
A. Assessment
B. Prevention
C. Treatment
D. Understanding
C. Treatment
Also Detection
2017_Drug Interactions and Pharmacovigilance
The reasons why premarketing trials cannot predict problems in drug prescribing is/are?
A. The effects of concomitant diseases and drugs are not normally studied.
A. The effects of concomitant diseases and drugs are not normally studied.
2017, 2018_Drug Interactions and Pharmacovigilance
Aim of pharmacovigilance covers the following:
A. Improvement of patient care and safety.
B. Cost effectiveness of drug prescribing
C. Effective communication to general public.
D. All of the above
D. All of the above
2017_Drug Interactions and Pharmacovigilance
The following statements is/are true of drug interactions:
B. These are interactions that can increase or decrease a drug’s efficacy.
B. These are interactions that can increase or decrease a drug’s efficacy.
2018_Drug Interactions and Pharmacovigilance
According to RA 8203, a counterfeit drug means
A. An imported drug that is not registered in the country
B. A medicinal product that has the correct ingredients but insufficient amount
C. A medicine that has the wrong constituents
D. AOTA
D. AOTA
2017_Drug Interactions and Pharmacovigilance
Medication errors cover the following events:
C. Product labeling and nomenclature
C. Product labeling and nomenclature
2017_Drug Interactions and Pharmacovigilance
Off label drug use can be motivated by:
A. Life threatening medical condition.
B. If pathologic/physiologic function of 2 diseases are similar.
C. Drugs not studied/approved for specific populations
D. All of the above
D. All of the above
2017_Drug Interactions and Pharmacovigilance
Based on the FDA advisory 2013-035 on treatment modalities outside standard medical care:
B. Food supplements without scientific basis are not considered standard of care.
B. Food supplements without scientific basis are not considered standard of care.
2017_Drug Interactions and Pharmacovigilance
Morbidity and mortality from poisoning cases can provide the following information:
A. Misuse and abuse of drugs
B. Counterfeit drugs
C. Substandard drugs
D. Adverse reactions
A. Misuse and abuse of drugs
2017_Drug Interactions and Pharmacovigilance
Direct pharmacodynamic drug interaction includes the following:
C. Drug-receptor reactions
C. Drug-receptor reactions
2017_Drug Interactions and Pharmacovigilance
The object drug has the following property/ies:
C. Low toxic/therapeutic ratio.
C. Low toxic/therapeutic ratio.
2017_Drug Interactions and Pharmacovigilance
Pharmaceutical drug interactions include the ff:
A. IV drug incompatibilities
B. Drug-container interaction
C. Drug-excipient interaction
D. All of the above.
D. All of the above
2017_Drug Interactions and Pharmacovigilance
Increasing awareness among clinicians on drug safety can be achieved through:
A. Access to reliable information
B. Communication with health professionals
C. Linking clinical findings with health policy
D. All of the above
D. All of the above
2017_Drug Interactions and Pharmacovigilance
The following is true of the effects brought about by drug interaction:
C. Potentiation means that the activity of one drug is increased by another drug that does not have the same activity.
C. Potentiation means that the activity of one drug is increased by another drug that does not have the same activity.
2017_Drug Interactions and Pharmacovigilance
Strategy/ies to avoid adverse drug interaction includes the following:
B. Be particularly careful when you prescribe to children, pregnant patients, elderly etc.
C. Review your patient regularly for all the drugs used.
D. All of the above
D. All of the above