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
126028271 12602827 1 I 20160717 20160725 20160728 20160728 EXP CO-ABBVIE-16P-036-1686251-00 ABBVIE 66.46 YR M Y 65.00000 KG 20160728 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
126028271 12602827 1 PS ZEMPLAR PARICALCITOL 1 Intravenous (not otherwise specified) POST DIALYSIS UNKNOWN 20819 5 UG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126028271 12602827 1 Hyperparathyroidism secondary

Outcome of event

Event ID CASEID OUTC COD
126028271 12602827 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126028271 12602827 Cardio-respiratory arrest
126028271 12602827 Respiratory distress

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
126028271 12602827 1 20130725 20160715 0