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
126906512 12690651 2 F 20160807 20160826 20160826 20160830 EXP VE-ABBVIE-16P-178-1710945-00 ABBVIE 72.50 YR F Y 0.00000 20160830 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
126906512 12690651 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
126906512 12690651 1 Nephropathy

Outcome of event

Event ID CASEID OUTC COD
126906512 12690651 OT
126906512 12690651 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126906512 12690651 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
126906512 12690651 1 20160126 20160804 0