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
114032573 11403257 3 F 20120726 20160816 20150821 20160824 EXP CA-ROCHE-1623324 ROCHE 54.86 YR F 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
114032573 11403257 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U 103976 150 MG SOLUTION FOR INJECTION
114032573 11403257 2 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 0
114032573 11403257 3 C PULMICORT TURBUHALER BUDESONIDE 1 0
114032573 11403257 4 C NASOCORT BUDESONIDE 1 0
114032573 11403257 5 C VENTOLIN ALBUTEROL SULFATE 1 Unknown COUPLE OF TIMES A DAY BUT OTHER DAYS MORE FREQUENTLY, QD 0 QD
114032573 11403257 6 C VENTOLIN ALBUTEROL SULFATE 1 Unknown 3 TIMES PER DAY 0 TID
114032573 11403257 7 C PREDNISONE. PREDNISONE 1 Unknown 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114032573 11403257 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
114032573 11403257 OT
114032573 11403257 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
114032573 11403257 Asthenia
114032573 11403257 Asthma
114032573 11403257 Decreased activity
114032573 11403257 Dyspnoea
114032573 11403257 Dyspnoea exertional
114032573 11403257 Fatigue
114032573 11403257 Lower respiratory tract infection
114032573 11403257 Pulmonary mass

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
114032573 11403257 1 20120726 0