+ Site Statistics
+ Search Articles
+ PDF Full Text Service
How our service works
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ Translate
+ Recently Requested

Are Food and Drug Administration prescription drug safety plans working? A case study of isotretinoin

Are Food and Drug Administration prescription drug safety plans working? A case study of isotretinoin

Pharmacoepidemiology and Drug Safety 22(12): 1258-1262

Please choose payment method:

(PDF emailed within 0-6 h: $19.90)

Accession: 051625335

Download citation: RISBibTeXText

PMID: 24115318

DOI: 10.1002/pds.3514

Related references

Reply letter: are FDA prescription drug safety plans working? A case study of isotretinoin. Pharmacoepidemiology and Drug Safety 23(4): 440-441, 2014

How does drug treatment for diabetes compare between Medicare Advantage prescription drug plans (MAPDs) and stand-alone prescription drug plans (PDPs)?. Health Services Research 48(3): 1057-1075, 2013

Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; policies, requirements, and administrative procedures. Food and Drug Administration, HHS. Final rule. Federal Register 64(232): 67720-67763, 2000

Transgender Patients, Isotretinoin, and US Food and Drug Administration-Mandated Risk Evaluation and Mitigation Strategies: A Prescription for Inclusion. JAMA Dermatology 152(5): 513-514, 2016

Off-label antidepressant prescription in pediatric outpatients based on China Food and Drug Administration and Food and Drug Administration regulations: a Chinese retrospective study. International Clinical Psychopharmacology 33(3): 172-179, 2018

The Prescription Drug User Fee Act: is a faster Food and Drug Administration always a better Food and Drug Administration?. Food and Drug Law Journal 60(2): 261-338, 2005

International Conference on Harmonisation; Electronic Transmission of Postmarket Individual Case Safety Reports for Drugs and Biologics, Excluding Vaccines; Availability of Food and Drug Administration Regional Implementation Specifications for ICH E2B(R3) Reporting to the Food and Drug Administration Adverse Event Reporting System. Notice of Availability. Federal Register 81(121): 40890-1, 2016

Food and Drug Administration Modernization Act of 1997; list of documents issued by the Food and Drug Administration that apply to medical devices regulated by the Center for Biologics Evaluation and Research. Food and Drug Administration, HHS. Notice. Federal Register 64(79): 20312-3, 1999

Medicare program; Medicare Advantage and prescription drug benefit programs: negotiated pricing and remaining revisions; prescription drug benefit program: payments to sponsors of retiree prescription drug plans. Final rule. Federal Register 77(8): 1877-1883, 2012

Prescription Drug Promotion from 2001-2014: Data from the U.S. Food and Drug Administration. Plos One 11(5): E0155035, 2017

High Prescription Drug Prices and the Influence of the Food and Drug Administration: In Response. Mayo Clinic Proceedings 79(4): 569-570, 2004

High prescription drug prices and the influence of the Food and Drug Administration. Mayo Clinic Proceedings 79(4): 569; Discussion 569-70, 2004

How the US Food and Drug Administration can solve the prescription drug shortage problem. American Journal of Public Health 103(5): E10-E14, 2013

Planning In The Food And Drug Administration For Regulation Of Prescription Drug Advertising. Current Therapeutic Research, Clinical and Experimental 7: 332-336, 1965

The Food and Drug Administration's regulation of prescription drug manufacturer speech: a First Amendment analysis. Food and Drug Law Journal 58(3): 365-437, 2003