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» Rudolph Joseph Maier, MD - Comment
Rudolph Joseph Maier, MD - Comment
Document ID:
FDA-2011-N-0802-0002
Document Type:
Public Submission
Agency:
Food And Drug Administration
Received Date:
November 29 2011, at 12:00 AM Eastern Standard Time
Date Posted:
February 28 2012, at 12:00 AM Eastern Standard Time
Comment Start Date:
November 17 2011, at 12:00 AM Eastern Standard Time
Comment Due Date:
June 12 2012, at 11:59 PM Eastern Standard Time
Tracking Number:
80f758d7
View Document:
This is comment on Notice
Role of Naloxone in OpioidOverdose Fatality Prevention; Workshop; Request for Comments
View Comment
The ready availability of naloxone to reverse intended or unintended overdose of opioids is to be encouraged. It is likely to save many lives and isn't likely to present a risk to the public. I urge it's acceptance by the FDA
Related Comments
View All
Total:
37
Rudolph Joseph Maier, MD - Comment
Public Submission
Posted:
02/28/2012
ID:
FDA-2011-N-0802-0002
Comment Period Closed
Jun 12,2012 11:59 PM ET
Pain Treatment Topics (Pain-Topics.org) - Comment
Public Submission
Posted:
04/12/2012
ID:
FDA-2011-N-0802-0003
Comment Period Closed
Jun 12,2012 11:59 PM ET
mark eisenberg - Comment
Public Submission
Posted:
04/12/2012
ID:
FDA-2011-N-0802-0005
Comment Period Closed
Jun 12,2012 11:59 PM ET
Mary Kay Borgstrom - Comment
Public Submission
Posted:
04/12/2012
ID:
FDA-2011-N-0802-0006
Comment Period Closed
Jun 12,2012 11:59 PM ET
Jeffrey Joseph Cece - Comment
Public Submission
Posted:
04/12/2012
ID:
FDA-2011-N-0802-0007
Comment Period Closed
Jun 12,2012 11:59 PM ET
Rudolph Joseph Maier, MD - Comment
This is comment on Notice
Role of Naloxone in OpioidOverdose Fatality Prevention; Workshop; Request for Comments
View Comment
Related Comments
View AllPublic Submission Posted: 02/28/2012 ID: FDA-2011-N-0802-0002
Jun 12,2012 11:59 PM ET
Public Submission Posted: 04/12/2012 ID: FDA-2011-N-0802-0003
Jun 12,2012 11:59 PM ET
Public Submission Posted: 04/12/2012 ID: FDA-2011-N-0802-0005
Jun 12,2012 11:59 PM ET
Public Submission Posted: 04/12/2012 ID: FDA-2011-N-0802-0006
Jun 12,2012 11:59 PM ET
Public Submission Posted: 04/12/2012 ID: FDA-2011-N-0802-0007
Jun 12,2012 11:59 PM ET