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
106731044 10673104 4 F 20140415 20160831 20141224 20160907 EXP CA-ROCHE-1433914 ROCHE 50.95 YR M Y 0.00000 20160907 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
106731044 10673104 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0068D 103976 150 MG SOLUTION FOR INJECTION
106731044 10673104 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0068D 103976 SOLUTION FOR INJECTION
106731044 10673104 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0068D 103976 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106731044 10673104 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
106731044 10673104 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106731044 10673104 Asthma
106731044 10673104 Blood pressure increased
106731044 10673104 Dysphagia
106731044 10673104 Fatigue
106731044 10673104 Feeling abnormal
106731044 10673104 Lung infection
106731044 10673104 Malaise
106731044 10673104 Muscle strain
106731044 10673104 Nasopharyngitis
106731044 10673104 Productive cough
106731044 10673104 Sputum discoloured
106731044 10673104 Throat tightness

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
106731044 10673104 1 20140415 0
106731044 10673104 2 20160809 0
106731044 10673104 3 20160831 0