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
117173702 11717370 2 F 20131211 20160826 20151110 20160901 EXP CA-ROCHE-1657447 ROCHE 40.02 YR F Y 0.00000 20160901 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
117173702 11717370 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976 375 MG SOLUTION FOR INJECTION QOW
117173702 11717370 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976 375 MG SOLUTION FOR INJECTION QOW
117173702 11717370 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117173702 11717370 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
117173702 11717370 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117173702 11717370 Anxiety
117173702 11717370 Cellulitis
117173702 11717370 Dizziness
117173702 11717370 Dyspnoea
117173702 11717370 Nausea
117173702 11717370 Sensitivity to weather change
117173702 11717370 Stress

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
117173702 11717370 1 20131020 0
117173702 11717370 2 20131120 0
117173702 11717370 3 20131211 0