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
127770851 12777085 1 I 20160913 20160923 20160923 20160923 EXP CO-ABBVIE-16P-036-1737176-00 ABBVIE 52.81 YR M Y 0.00000 20160923 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
127770851 12777085 1 PS ZEMPLAR PARICALCITOL 1 Unknown POST DIALYSIS D UNKNOWN 20819 5 UG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127770851 12777085 1 Hyperparathyroidism secondary

Outcome of event

Event ID CASEID OUTC COD
127770851 12777085 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127770851 12777085 Cardiac arrest
127770851 12777085 Respiratory distress
127770851 12777085 Tachycardia

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
127770851 12777085 1 20150831 20160913 0