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
106534584 10653458 4 F 2013 20160711 20141216 20160720 EXP CA-ROCHE-1253615 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
106534584 10653458 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous 103976 300 MG SOLUTION FOR INJECTION QOW
106534584 10653458 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous 103976 225 MG SOLUTION FOR INJECTION QOW
106534584 10653458 3 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
106534584 10653458 4 C ALVESCO CICLESONIDE 1 0
106534584 10653458 5 C SINGULAIR MONTELUKAST SODIUM 1 0
106534584 10653458 6 C PREDNISONE. PREDNISONE 1 0
106534584 10653458 7 C BRICANYL TERBUTALINE SULFATE 1 0
106534584 10653458 8 C LEVAQUIN LEVOFLOXACIN 1 0
106534584 10653458 9 C CLAVULIN AMOXICILLINCLAVULANIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106534584 10653458 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
106534584 10653458 OT
106534584 10653458 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
106534584 10653458 Abdominal pain
106534584 10653458 Abnormal faeces
106534584 10653458 Bronchitis
106534584 10653458 Cough
106534584 10653458 Cystic fibrosis
106534584 10653458 Forced expiratory volume decreased
106534584 10653458 Weight increased

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
106534584 10653458 1 20081113 0
106534584 10653458 2 20090514 0