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
125156172 12515617 2 F 20160522 20160701 20160630 20160701 EXP CO-ABBVIE-16P-036-1664569-00 ABBVIE 66.12 YR F Y 0.00000 20160701 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
125156172 12515617 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
125156172 12515617 1 Hyperparathyroidism secondary

Outcome of event

Event ID CASEID OUTC COD
125156172 12515617 DE
125156172 12515617 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125156172 12515617 Anal incontinence
125156172 12515617 Cardio-respiratory arrest
125156172 12515617 Urinary tract infection

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
125156172 12515617 1 20150511 20160311 0