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
102827943 10282794 3 F 20160805 20140708 20160810 EXP JP-ROCHE-1431350 ROCHE 83.00 YR F Y 0.00000 20160810 MD JP JP

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
102827943 10282794 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous 103976 SOLUTION FOR INJECTION
102827943 10282794 2 C ADOAIR FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
102827943 10282794 3 C MEDROL METHYLPREDNISOLONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102827943 10282794 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
102827943 10282794 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
102827943 10282794 Asthma

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found