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
94350962 9435096 2 F 20130730 20130801 20160909 EXP US-ROCHE-1255178 ROCHE 0.00 M Y 0.00000 20160909 CN US US

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
94350962 9435096 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous UNKNOWN 103976 375 MG SOLUTION FOR INJECTION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
94350962 9435096 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
94350962 9435096 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
94350962 9435096 Asthma

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

no results found

Therapies reported

no results found