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
74622367 7462236 7 F 201203 20160826 20100709 20160831 EXP CA-ROCHE-GNE303759 ROCHE 60.77 YR F Y 0.00000 20160901 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
74622367 7462236 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062,S0001E 103976 150 MG SOLUTION FOR INJECTION
74622367 7462236 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062,S0001E 103976 SOLUTION FOR INJECTION
74622367 7462236 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062,S0001E 103976 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
74622367 7462236 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
74622367 7462236 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
74622367 7462236 Bronchitis
74622367 7462236 Cough
74622367 7462236 Pneumonia
74622367 7462236 Productive cough
74622367 7462236 Seasonal allergy
74622367 7462236 Sinusitis
74622367 7462236 Tremor

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
74622367 7462236 1 20090421 0
74622367 7462236 2 20160408 0
74622367 7462236 3 20160729 0