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
105238878 10523887 8 F 20140523 20160624 20141017 20160701 EXP CA-ROCHE-1475932 ROCHE 13.19 YR F Y 0.00000 20160701 MD 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
105238878 10523887 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062 103976 300 MG
105238878 10523887 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062 103976
105238878 10523887 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062 103976
105238878 10523887 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062 103976
105238878 10523887 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062 103976
105238878 10523887 6 C AVAMYS FLUTICASONE FUROATE 1 Nasal UNK U 0 SUSPENSION AND SOLUTION FOR SPRAY

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105238878 10523887 1 Asthma
105238878 10523887 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
105238878 10523887 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105238878 10523887 Asthma
105238878 10523887 Blood pressure diastolic decreased
105238878 10523887 Body temperature decreased
105238878 10523887 Chest pain
105238878 10523887 Middle insomnia
105238878 10523887 Rhinitis allergic
105238878 10523887 Varicella

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
105238878 10523887 1 20140116 0
105238878 10523887 2 20140228 0
105238878 10523887 3 20140523 0
105238878 10523887 4 20140620 0
105238878 10523887 5 20160401 0