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
94500302 9450030 2 F 20130724 20160810 20130809 20160817 EXP CA-ROCHE-1259616 ROCHE 36.11 YR F Y 0.00000 20160817 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
94500302 9450030 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976 300 MG SOLUTION FOR INJECTION QOW
94500302 9450030 2 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown U 0
94500302 9450030 3 C ALVESCO CICLESONIDE 1 Unknown U 0
94500302 9450030 4 C SINGULAIR MONTELUKAST SODIUM 1 Unknown U 0
94500302 9450030 5 C REACTINE (CANADA) CETIRIZINE HYDROCHLORIDE 1 Unknown U 0
94500302 9450030 6 C ATROVENT IPRATROPIUM BROMIDE 1 Unknown U 0
94500302 9450030 7 C VENTOLIN ALBUTEROL SULFATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
94500302 9450030 1 Asthma
94500302 9450030 2 Product used for unknown indication
94500302 9450030 3 Product used for unknown indication
94500302 9450030 4 Product used for unknown indication
94500302 9450030 5 Product used for unknown indication
94500302 9450030 6 Product used for unknown indication
94500302 9450030 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
94500302 9450030 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
94500302 9450030 Abdominal discomfort
94500302 9450030 Pneumonia

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
94500302 9450030 1 20130724 0