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
98004664 9800466 4 F 20160712 20140107 20160720 EXP CA-ROCHE-1330001 ROCHE 0.00 F Y 0.00000 20160720 OT CA CA

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
98004664 9800466 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976 300 MG
98004664 9800466 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976
98004664 9800466 3 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown U 0
98004664 9800466 4 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98004664 9800466 1 Asthma
98004664 9800466 3 Product used for unknown indication
98004664 9800466 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
98004664 9800466 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
98004664 9800466 Gait disturbance
98004664 9800466 General physical health deterioration
98004664 9800466 Influenza
98004664 9800466 Malaise
98004664 9800466 Pain in extremity
98004664 9800466 Road traffic accident

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
98004664 9800466 1 20110428 0
98004664 9800466 2 20140120 0