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
109593293 10959329 3 F 201602 20160909 20150327 20160916 EXP CA-ROCHE-1556971 ROCHE 64.79 YR F Y 0.00000 20160916 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
109593293 10959329 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976 300 MG SOLUTION FOR INJECTION
109593293 10959329 2 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
109593293 10959329 3 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0
109593293 10959329 4 C SALBUTAMOL ALBUTEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109593293 10959329 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
109593293 10959329 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
109593293 10959329 Bronchitis
109593293 10959329 Inflammation
109593293 10959329 Lung disorder
109593293 10959329 Mental disorder

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
109593293 10959329 1 20140729 0