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Celtoi Celtoi
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7 years ago
The FDA may require the manufacture of a drug to post a prominent “black box” warning when:
a.   The drug receives IND status (Investigational new drug)
b.   Following phase one human testing
c.   Unlabeled uses of the drug occur
d.   A problem may arise that may lead to death or severe injury if the medication is used
Textbook 
Prehospital Emergency Pharmacology

Prehospital Emergency Pharmacology


Edition: 7th
Authors:
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beiersdorf_191beiersdorf_191
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7 years ago
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Celtoi Author
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7 years ago
this is exactly what I needed
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Smart ... Thanks!
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2 hours ago
This site is awesome
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