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
125669982 12566998 2 F 20160609 20160824 20160718 20160826 EXP VE-ABBVIE-16P-178-1678171-00 ABBVIE 68.79 YR F Y 0.00000 20160826 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
125669982 12566998 1 PS ZEMPLAR PARICALCITOL 1 Unknown UNKNOWN 20819 INJECTION
125669982 12566998 2 C VITAMIN B12 CYANOCOBALAMIN 1 0
125669982 12566998 3 C FOLIC ACID. FOLIC ACID 1 0
125669982 12566998 4 C BROMAZEPAM BROMAZEPAM 1 0
125669982 12566998 5 C NIFEDIPINE. NIFEDIPINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125669982 12566998 1 Nephropathy
125669982 12566998 2 Product used for unknown indication
125669982 12566998 3 Product used for unknown indication
125669982 12566998 4 Product used for unknown indication
125669982 12566998 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125669982 12566998 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125669982 12566998 Cardiac failure

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
125669982 12566998 1 20080701 20151001 0