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
125657891 12565789 1 I 20160605 20160714 20160718 20160718 EXP AR-ABBVIE-16P-007-1677767-00 ABBVIE 70.25 YR F Y 0.00000 20160718 CN COUNTRY NOT SPECIFIED AR

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
125657891 12565789 1 PS ZEMPLAR PARICALCITOL 1 Intravenous (not otherwise specified) UNKNOWN 20819 5 UG INJECTION TIW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125657891 12565789 1 Chronic kidney disease

Outcome of event

Event ID CASEID OUTC COD
125657891 12565789 OT
125657891 12565789 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125657891 12565789 Cardiac arrest

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
125657891 12565789 1 20140102 0