What does CVADR mean?
CVADR means cardiovascular adverse drug reaction
This acronym/slang usually belongs to Medical & Science category.
What is the abbreviation for cardiovascular adverse drug reaction?
cardiovascular adverse drug reaction can be abbreviated as CVADR
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Most popular questions people look for before coming to this page
Q: A: |
What does CVADR stand for? CVADR stands for "cardiovascular adverse drug reaction". |
Q: A: |
How to abbreviate "cardiovascular adverse drug reaction"? "cardiovascular adverse drug reaction" can be abbreviated as CVADR. |
Q: A: |
What is the meaning of CVADR abbreviation? The meaning of CVADR abbreviation is "cardiovascular adverse drug reaction". |
Q: A: |
What is CVADR abbreviation? One of the definitions of CVADR is "cardiovascular adverse drug reaction". |
Q: A: |
What does CVADR mean? CVADR as abbreviation means "cardiovascular adverse drug reaction". |
Q: A: |
What is shorthand of cardiovascular adverse drug reaction? The most common shorthand of "cardiovascular adverse drug reaction" is CVADR. |
Abbreviations or Slang with similar meaning
- ADRSP - Adverse Drug Reaction Surveillance Program
- CADRMP - Canadian Adverse Drug Reaction Monitoring Program
- AADR - Acute Adverse Drug Reaction
- ADR - Adverse Drug Reaction
- ADRM - Adverse Drug Reaction Monitoring
- ADROIT - Adverse Drug Reaction On-Line Information Tracking
- CADRIS - Canadian Adverse Drug Reaction Information System
- IADR - Idiosyncratic Adverse Drug Reaction
- SADR - Serious Adverse Drug Reaction
- ADRU - Adverse Drug Reaction Unit
- ADRES - Adverse Drug Reaction Electronic System
- CADRAC - Canadian Adverse Drug Reaction Advisory Committee
- NADRAC - National Adverse Drug Reaction Advisory Committee
- SADRAC - Swedish Adverse Drug Reaction Advisory Committee
- UADR - Unexpected Adverse Drug Reaction
- ADRD - Adverse Drug Reaction Database
- ADRs - adverse drug reaction
- adrs - Adverse Drug Reaction Surveillance
- SADR - Suspected Adverse Drug Reaction
- 1932 - FDA form for veterinary adverse drug reaction, lack of effectiveness, product defect report--mandatory