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
125507641 12550764 1 I 20160705 20160711 20160712 20160712 EXP CO-ABBVIE-16P-036-1674639-00 ABBVIE 23.23 YR M Y 0.00000 20160712 OT COUNTRY NOT SPECIFIED CO

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
125507641 12550764 1 PS ZEMPLAR PARICALCITOL 1 Intravenous (not otherwise specified) UNKNOWN 20819 10 UG SOLUTION FOR INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125507641 12550764 1 Hyperparathyroidism secondary

Outcome of event

Event ID CASEID OUTC COD
125507641 12550764 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125507641 12550764 Asthenia
125507641 12550764 Cardio-respiratory arrest
125507641 12550764 Tachyarrhythmia

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
125507641 12550764 1 20150818 20160307 0