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
118249602 11824960 2 F 20151118 20151229 20151210 20160101 EXP SE-ROCHE-1675667 ROCHE 49.00 YR F Y 0.00000 20160101 MD SE SE

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
118249602 11824960 1 PS XOLAIR OMALIZUMAB 1 Unknown BATCHNR EFTERSOKS 103976
118249602 11824960 2 SS XOLAIR OMALIZUMAB 1 BATCHNR EFTERSOKS 103976
118249602 11824960 3 C BETAPRED BETAMETHASONE SODIUM PHOSPHATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118249602 11824960 1 Asthma
118249602 11824960 2 Hypersensitivity

Outcome of event

Event ID CASEID OUTC COD
118249602 11824960 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118249602 11824960 Feeling hot
118249602 11824960 Swelling face
118249602 11824960 Throat irritation

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
118249602 11824960 1 20151117 0