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
120826083 12082608 3 F 201604 20160815 20160217 20160819 EXP CA-ROCHE-1712507 ROCHE 29.03 YR F Y 0.00000 20160819 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
120826083 12082608 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0066B 103976 300 MG SOLUTION FOR INJECTION
120826083 12082608 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0066B 103976 SOLUTION FOR INJECTION
120826083 12082608 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0066B 103976 SOLUTION FOR INJECTION
120826083 12082608 4 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 0
120826083 12082608 5 C VENTOLINE ALBUTEROL 1 0
120826083 12082608 6 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
120826083 12082608 7 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120826083 12082608 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
120826083 12082608 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120826083 12082608 Asthma
120826083 12082608 Bronchitis
120826083 12082608 Forced expiratory volume decreased
120826083 12082608 Headache
120826083 12082608 Lung disorder
120826083 12082608 Nasal congestion
120826083 12082608 Peripheral swelling

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
120826083 12082608 1 20150721 0
120826083 12082608 2 20160112 0
120826083 12082608 3 20160503 0