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
125902541 12590254 1 I 201605 20160721 20160725 20160725 EXP AR-ABBVIE-16P-007-1684621-00 ABBVIE 76.18 YR F Y 0.00000 20160725 CN COUNTRY NOT SPECIFIED AR

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
125902541 12590254 1 PS ZEMPLAR PARICALCITOL 1 Intravenous (not otherwise specified) UNKNOWN 20819 5 UG INJECTION TIW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125902541 12590254 1 Hyperparathyroidism secondary

Outcome of event

Event ID CASEID OUTC COD
125902541 12590254 OT
125902541 12590254 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125902541 12590254 Bronchitis
125902541 12590254 Fall
125902541 12590254 Pelvic fracture
125902541 12590254 Pneumonia

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
125902541 12590254 1 20150201 0