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
113226658 11322665 8 F 20130614 20160621 20150730 20160701 EXP CA-ROCHE-1614436 ROCHE 53.45 YR F Y 0.00000 20160701 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
113226658 11322665 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0059B,S0062 103976 375 MG SOLUTION FOR INJECTION QOW
113226658 11322665 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0059B,S0062 103976 SOLUTION FOR INJECTION
113226658 11322665 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0059B,S0062 103976 SOLUTION FOR INJECTION
113226658 11322665 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0059B,S0062 103976 SOLUTION FOR INJECTION
113226658 11322665 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0059B,S0062 103976 SOLUTION FOR INJECTION
113226658 11322665 6 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0059B,S0062 103976 SOLUTION FOR INJECTION
113226658 11322665 7 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0059B,S0062 103976 SOLUTION FOR INJECTION
113226658 11322665 8 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0059B,S0062 103976 SOLUTION FOR INJECTION
113226658 11322665 9 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0059B,S0062 103976 SOLUTION FOR INJECTION
113226658 11322665 10 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
113226658 11322665 11 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0
113226658 11322665 12 C SINGULAIR MONTELUKAST SODIUM 1 0
113226658 11322665 13 C VENTOLIN ALBUTEROL SULFATE 1 0
113226658 11322665 14 C AVAMYS FLUTICASONE FUROATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113226658 11322665 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
113226658 11322665 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113226658 11322665 Asthenia
113226658 11322665 Asthma
113226658 11322665 Blood pressure decreased
113226658 11322665 Bronchitis
113226658 11322665 Dyspnoea
113226658 11322665 Eczema
113226658 11322665 Erythema
113226658 11322665 Fall
113226658 11322665 Fatigue
113226658 11322665 Heart rate increased
113226658 11322665 Hypersensitivity
113226658 11322665 Hyposmia
113226658 11322665 Infection
113226658 11322665 Influenza
113226658 11322665 Injection site erythema
113226658 11322665 Injection site oedema
113226658 11322665 Injection site pain
113226658 11322665 Injection site pruritus
113226658 11322665 Joint dislocation
113226658 11322665 Myalgia
113226658 11322665 Nasal discharge discolouration
113226658 11322665 Pruritus
113226658 11322665 Pyrexia
113226658 11322665 Rash

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
113226658 11322665 1 20130319 0
113226658 11322665 2 20130614 0
113226658 11322665 3 20140108 0
113226658 11322665 4 20140417 0
113226658 11322665 5 20140514 0
113226658 11322665 6 20150102 0
113226658 11322665 7 20150119 0
113226658 11322665 8 20150914 0
113226658 11322665 9 20160404 0