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
100942614 10094261 4 F 20160823 20140422 20160830 EXP BR-ROCHE-1347162 ROCHE 0.00 F Y 70.00000 KG 20160830 CN BR BR

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
100942614 10094261 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous 1 DF, QMO U 103976 1 DF SOLUTION FOR INJECTION /month
100942614 10094261 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous 150 MG, QMO U 103976 150 MG SOLUTION FOR INJECTION /month
100942614 10094261 3 C CAPTOPRIL. CAPTOPRIL 1 Unknown UNK (STARTED 5 YEARS AGO) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100942614 10094261 1 Asthma
100942614 10094261 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
100942614 10094261 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100942614 10094261 Asthmatic crisis
100942614 10094261 Blood pressure increased
100942614 10094261 Breath sounds abnormal
100942614 10094261 Diabetes mellitus
100942614 10094261 Visual impairment
100942614 10094261 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found