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
102344765 10234476 5 F 20160829 20140613 20160902 EXP CA-ROCHE-1417834 ROCHE 0.00 F Y 0.00000 20160902 OT 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
102344765 10234476 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062 103976 150 MG SOLUTION FOR INJECTION
102344765 10234476 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062 103976 SOLUTION FOR INJECTION
102344765 10234476 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062 103976 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102344765 10234476 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
102344765 10234476 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
102344765 10234476 Asthma
102344765 10234476 Drug effect decreased
102344765 10234476 Dyspnoea
102344765 10234476 Forced expiratory volume decreased
102344765 10234476 Malaise
102344765 10234476 Middle insomnia
102344765 10234476 Sinusitis
102344765 10234476 Weight decreased

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
102344765 10234476 1 20140325 0
102344765 10234476 2 20150423 0
102344765 10234476 3 20160302 0