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
112647652 11264765 2 F 20150502 20160629 20150713 20160707 EXP CA-ROCHE-1607367 ROCHE 34.66 YR F Y 0.00000 20160707 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
112647652 11264765 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous POWDER AND SOLVENT FOR SOLUTION FOR INJECTION U 103976 300 MG SOLUTION FOR INJECTION
112647652 11264765 2 SS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 Intravenous (not otherwise specified) U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112647652 11264765 1 Asthma
112647652 11264765 2 Dyspnoea

Outcome of event

Event ID CASEID OUTC COD
112647652 11264765 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
112647652 11264765 Asthma
112647652 11264765 Drug ineffective
112647652 11264765 Heart rate increased
112647652 11264765 Hypersensitivity
112647652 11264765 Lung infection
112647652 11264765 Nausea
112647652 11264765 White blood cell count increased

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
112647652 11264765 1 20140702 0