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
121255904 12125590 4 F 201410 20160705 20160229 20160712 EXP CA-ROCHE-1717659 ROCHE 41.34 YR F Y 0.00000 20160712 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
121255904 12125590 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0060,S0060,S0062 103976 300 MG SOLUTION FOR INJECTION
121255904 12125590 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0060,S0060,S0062 103976 SOLUTION FOR INJECTION
121255904 12125590 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0060,S0060,S0062 103976 SOLUTION FOR INJECTION
121255904 12125590 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0060,S0060,S0062 103976 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121255904 12125590 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
121255904 12125590 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121255904 12125590 Asthenia
121255904 12125590 Asthma
121255904 12125590 Chest discomfort
121255904 12125590 Fatigue
121255904 12125590 Feeling abnormal
121255904 12125590 Headache
121255904 12125590 Lower respiratory tract infection
121255904 12125590 Nasopharyngitis
121255904 12125590 Pruritus
121255904 12125590 Vision blurred

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
121255904 12125590 1 20140415 0
121255904 12125590 2 20151229 0
121255904 12125590 3 20160126 0
121255904 12125590 4 20160419 0