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
98478707 9847870 7 F 20140115 20160915 20140128 20160921 EXP CA-ROCHE-1339789 ROCHE 41.01 YR F Y 0.00000 20160922 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
98478707 9847870 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976 225 MG SOLUTION FOR INJECTION QOW
98478707 9847870 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976 SOLUTION FOR INJECTION
98478707 9847870 3 C SINGULAIR MONTELUKAST SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98478707 9847870 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
98478707 9847870 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
98478707 9847870 Alopecia
98478707 9847870 Asthma
98478707 9847870 Chest discomfort
98478707 9847870 Dysphonia
98478707 9847870 Dyspnoea
98478707 9847870 Fall
98478707 9847870 Fatigue
98478707 9847870 Loss of consciousness
98478707 9847870 Malaise
98478707 9847870 Respiratory disorder
98478707 9847870 Sensitivity to weather change
98478707 9847870 Tremor
98478707 9847870 Upper limb fracture

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
98478707 9847870 1 20140109 0
98478707 9847870 2 20160518 0