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
115952942 11595294 2 F 2013 20160720 20151006 20160726 EXP CA-ROCHE-1641632 ROCHE 49.14 YR M Y 0.00000 20160726 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
115952942 11595294 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous 103976 300 MG SOLUTION FOR INJECTION
115952942 11595294 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous 103976 300 MG SOLUTION FOR INJECTION
115952942 11595294 3 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 0
115952942 11595294 4 C NASONEX MOMETASONE FUROATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115952942 11595294 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
115952942 11595294 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115952942 11595294 Drug ineffective
115952942 11595294 Sinusitis
115952942 11595294 Weight decreased
115952942 11595294 Weight increased

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
115952942 11595294 1 20111222 0
115952942 11595294 2 20160630 20160630 0