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
126088061 12608806 1 I 20160605 20160613 20160729 20160729 EXP CO-ABBVIE-16P-036-1652573-00 ABBVIE 60.70 YR F Y 0.00000 20160729 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
126088061 12608806 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
126088061 12608806 1 Hyperparathyroidism secondary

Outcome of event

Event ID CASEID OUTC COD
126088061 12608806 DE
126088061 12608806 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126088061 12608806 Cerebrovascular accident
126088061 12608806 Respiratory failure

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
126088061 12608806 1 20150831 20160603 0