What does 3500 mean Governmental FDA ?
This is a page where explained definition of 3500 - acronym, abbreviation or shorthand form.
On this page you can see detailed information about 3500 as it is used in Governmental- FDA sector.
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3500 in Governmental FDA means:
FDA form for voluntary reporting of adverse events
3500 in Governmental FDA stands for: FDA form for voluntary reporting of adverse events, but what about the same or alike Acronyms?
Maybe you are also interested other acronyms like 3500 which are used with different definition and different situations? Here they are, below.
|Short form||Meaning||Category||Second Category|
|3500||Means||FDA form for voluntary reporting of adverse events||Governmental||FDA|
|3500A||Means||FDA form for mandatory reporting of adverse events||Governmental||FDA|
|FORM 3500||Means||Voluntary Reporting of Adverse Events||Governmental||FDA|
|FD-1932a||Means||FDA form, Veterinary Adverse Drug Reaction, lack of effectiveness, product defect report - Voluntary||Governmental||FDA|
|1932a||Means||FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--voluntary||Governmental||FDA|
|FD-1932a||Means||FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report - voluntary||Governmental||FDA|
|FAERS||Means||FDA Adverse Event Reporting System||Governmental||FDA|
|MEDWATCH||Means||FDA Safety Information and Adverse Event Reporting Program||Governmental||FDA|
|FD-1932||Means||FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory||Governmental||US Government|
|FD-1932||Means||FDA form, Veterinary Adverse Drug Reaction, lack of effectiveness, product defect report - Mandatory||Governmental||FDA|
|FORM 3500A||Means||Mandatory Reporting of Adverse Events||Governmental||FDA|
|VAERS||Means||Vaccine Adverse Events Reporting System||Medical||British Medicine|
|482||Means||FDA form for notice of inspection||Governmental||FDA|
|AEFI||Means||Adverse Events Following Immunization||Miscellaneous||Unclassified|
|AEP||Means||Adverse Events Profile||Medical||Hospitals|
|OAE||Means||Ontology of Adverse Events||Miscellaneous||Unclassified|
|ADE||Means||Adverse Drug Events||Medical||Drugs|
|AEFI||Means||Adverse Events Following Immunisation||Miscellaneous||Unclassified|
|FD-356V||Means||FDA form, New Animal Drug Application||Governmental||FDA|
|356V||Means||FDA form for new animal drug appication||Governmental||FDA|
|FD-356V||Means||FDA form for new animal drug application||Governmental||US Government|
|MACE||Means||Major Adverse Cardiac Events||Medical||Cardiology|
|WDAE||Means||Withdrawal Due to Adverse Events||Medical|
|NSAE||Means||Nurse Sensitive Adverse Events||Medical||Nursing|
|TEAE||Means||treatment emergent adverse events||Miscellaneous||Unclassified|