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Package Inserts

Known as: Insert, Package, Inserts, Package, Package Insert 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
To evaluate the safety‐related regulatory actions implemented by Japan's Pharmaceuticals and Medical Devices Agency (PMDA) in… 
Review
2016
Review
2016
Background Package inserts (PIs) should promote the safe and effective use of medicines. The comprehension of PIs is related to… 
Review
2013
Review
2013
* Abbreviations: BPCA — : Best Pharmaceuticals for Children Act FDA — : Food and Drug Administration MC — : Molluscum… 
2010
2010
OBJECTIVES Package inserts are the most frequent source of patient information about medicines aside from doctors and pharmacists… 
Review
2010
Review
2010
The Trial to Reduce Cardiovascular Endpoints with Aranesp Therapy (TREAT) (1) has prompted the Food and Drug Administration (FDA… 
2006
2006
German regulations demand an extensive package insert for drugs. However, to what extent the information given is used and what… 
Review
2003
Review
2003
Objective: To examine public opinion in Saudi Arabia regarding the technical drug package insert (PI) as a source of information… 
1989
1989
The health authorities of Belgium, a European country with a population of 10 million and 3 national languages, decided in 1984… 
1984
1984
  • Joubert PhD. Skene
  • 1984
  • Corpus ID: 32795502
One thousand questionnaires were distributed to private medical practitioners by representatives of a pharmaceutical company. The… 
1975
1975
The Food and Drug Administration (FDA), as the government regulatory agency responsible for labeling prescription drugs for safe…