The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126876962 12687696 2 F 20160822 20160826 20160825 20160829 EXP VE-ABBVIE-16P-178-1710931-00 ABBVIE 63.73 YR F Y 0.00000 20160829 MD COUNTRY NOT SPECIFIED VE

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126876962 12687696 1 PS ZEMPLAR PARICALCITOL 1 Intravenous (not otherwise specified) 5 MCG/ML 447398E02 20819 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126876962 12687696 1 Nephropathy

Outcome of event

Event ID CASEID OUTC COD
126876962 12687696 DE
126876962 12687696 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126876962 12687696 Cardiac disorder

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126876962 12687696 1 20121001 20160818 0