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
119422567 11942256 7 F 20150609 20160816 20160125 20160823 EXP CA-ROCHE-1698074 ROCHE 60.99 YR M Y 0.00000 20160824 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
119422567 11942256 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062,S0068D,S0003B 103976 375 MG SOLUTION FOR INJECTION QOW
119422567 11942256 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0062,S0068D,S0003B 103976 SOLUTION FOR INJECTION
119422567 11942256 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0062,S0068D,S0003B 103976 SOLUTION FOR INJECTION
119422567 11942256 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0062,S0068D,S0003B 103976 SOLUTION FOR INJECTION
119422567 11942256 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0062,S0068D,S0003B 103976 375 MG SOLUTION FOR INJECTION QOW
119422567 11942256 6 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown UNK U 0
119422567 11942256 7 C SINGULAIR MONTELUKAST SODIUM 1 Unknown UNK U 0
119422567 11942256 8 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Unknown U 0
119422567 11942256 9 C VENTOLIN ALBUTEROL SULFATE 1 Unknown UNK U 0
119422567 11942256 10 C RAMIPRIL. RAMIPRIL 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119422567 11942256 1 Asthma
119422567 11942256 6 Product used for unknown indication
119422567 11942256 7 Product used for unknown indication
119422567 11942256 8 Product used for unknown indication
119422567 11942256 9 Product used for unknown indication
119422567 11942256 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119422567 11942256 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119422567 11942256 Blood pressure increased
119422567 11942256 Deafness unilateral
119422567 11942256 Drug ineffective
119422567 11942256 Ear infection
119422567 11942256 Fatigue
119422567 11942256 Lung disorder
119422567 11942256 Nasal congestion
119422567 11942256 Psoriasis
119422567 11942256 Pulmonary congestion
119422567 11942256 Urticaria

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
119422567 11942256 1 20150609 0
119422567 11942256 2 20160303 0
119422567 11942256 3 20160512 0
119422567 11942256 4 20160707 0
119422567 11942256 5 20160721 20160721 0