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
125584012 12558401 2 F 20160618 20160715 20160714 20160715 EXP CO-ABBVIE-16P-036-1676468-00 ABBVIE 65.81 YR M Y 0.00000 20160715 CN 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
125584012 12558401 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
125584012 12558401 1 Hyperparathyroidism secondary

Outcome of event

Event ID CASEID OUTC COD
125584012 12558401 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125584012 12558401 Choking
125584012 12558401 Cough
125584012 12558401 Pneumonia bacterial
125584012 12558401 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
125584012 12558401 1 20160512 20160616 0