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
1021302810 10213028 10 F 20140514 20150922 20140603 20150930 EXP CA-ROCHE-1411736 ROCHE 63.12 YR F Y 0.00000 20150930 N CN 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
1021302810 10213028 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous VIAL D S0021A 103976 375 MG QOW
1021302810 10213028 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous D S0021A 103976 375 MG
1021302810 10213028 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous D S0021A 103976
1021302810 10213028 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous D S0021A 103976
1021302810 10213028 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous D S0021A 103976
1021302810 10213028 6 SS XOLAIR OMALIZUMAB 1 Subcutaneous D S0021A 103976

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1021302810 10213028 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
1021302810 10213028 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1021302810 10213028 Adrenal disorder
1021302810 10213028 Aspergillus infection
1021302810 10213028 Asthma
1021302810 10213028 Bile duct obstruction
1021302810 10213028 Body temperature decreased
1021302810 10213028 Drug hypersensitivity
1021302810 10213028 Psoriasis

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
1021302810 10213028 1 20130904 0
1021302810 10213028 2 20140514 0
1021302810 10213028 3 20140805 0
1021302810 10213028 4 20141001 0
1021302810 10213028 5 20141029 0
1021302810 10213028 6 20141210 0