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
125682691 12568269 1 I 20160701 20160715 20160718 20160718 EXP VE-ABBVIE-16P-178-1678158-00 ABBVIE 58.87 YR M Y 0.00000 20160718 CN 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
125682691 12568269 1 PS ZEMPLAR PARICALCITOL 1 Unknown UNKNOWN 20819 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125682691 12568269 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125682691 12568269 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125682691 12568269 Cardiac failure

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

no results found

Therapies reported

no results found