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
125294392 12529439 2 F 20160622 20160727 20160706 20160801 EXP US-ROCHE-1787702 ROCHE 41.76 YR M Y 81.72000 KG 20160801 CN US US

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
125294392 12529439 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous N UNKNOWN 103976 350 MG SOLUTION FOR INJECTION
125294392 12529439 2 SS KLONOPIN CLONAZEPAM 1 Oral AS REQUIRED U 17533 1 MG TABLET
125294392 12529439 3 C ALLEGRA FEXOFENADINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125294392 12529439 1 Chronic spontaneous urticaria
125294392 12529439 2 Anxiety

Outcome of event

Event ID CASEID OUTC COD
125294392 12529439 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125294392 12529439 Anxiety
125294392 12529439 Blood pressure fluctuation
125294392 12529439 Chest pain
125294392 12529439 Dizziness
125294392 12529439 Dyspnoea
125294392 12529439 Malaise
125294392 12529439 Myalgia
125294392 12529439 Nausea

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
125294392 12529439 1 20160615 0