This decision was released via conference call. You can listen to the call at 1-866-419-2678.
The actions were swift when the decision to ban the products came out. The FDA said that they were unaware of the unique needs of terminal patients and that they have immediately reinstated the manufacturing of 20 mg/ml morphine sulfate solution.
In the original decision, no representatives from hospice or palliative care organizations were included.
This particular omission is expected to be corrected in future summits.
The FDA said it was sorry for the disruption. They were not aware of the disruption in patient care the ruling would cause or that there was already a critical shortage in some lines of medications.
The FDA is interested of any drug shortages in your area including the management of patients. If there are any you can let them know by e-mailing them at drugshortages@fda.hhs.gov.
Reference: http://fda.com/
Published by Gary Davis
Retired Insurance CEO. Trained in medicine and medicines. Trained in mental health particularly manic depression as well as most illnesses (from medical underwriting. Business owner, business, marketing,... View profile
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- fda.com/
- 1-866-419-2678.
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