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
126681511 12668151 1 I 20160718 20160818 20160819 20160819 EXP VE-ABBVIE-16P-178-1705720-00 ABBVIE 57.51 YR F Y 0.00000 20160819 OT COUNTRY NOT SPECIFIED VE

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
126681511 12668151 1 PS ZEMPLAR PARICALCITOL 1 Intravenous (not otherwise specified) UNKNOWN 20819 INJECTION
126681511 12668151 2 C PREDNISONE. PREDNISONE 1 0
126681511 12668151 3 C OLMESARTAN OLMESARTAN 1 0
126681511 12668151 4 C ERYTHROPOIETIN ERYTHROPOIETIN 1 0
126681511 12668151 5 C HEPARIN HEPARIN SODIUM 1 0
126681511 12668151 6 C FOLIC ACID. FOLIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126681511 12668151 1 Product used for unknown indication
126681511 12668151 2 Product used for unknown indication
126681511 12668151 3 Product used for unknown indication
126681511 12668151 4 Product used for unknown indication
126681511 12668151 5 Product used for unknown indication
126681511 12668151 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126681511 12668151 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126681511 12668151 Pneumonia
126681511 12668151 Sepsis

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
126681511 12668151 1 20160201 0