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
118663806 11866380 6 F 2012 20160908 20151224 20160915 EXP CA-ROCHE-1680862 ROCHE 69.44 YR F Y 57.00000 KG 20160915 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
118663806 11866380 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous U S0078,S0062,S0066B,S0003B 103976 300 MG SOLUTION FOR INJECTION
118663806 11866380 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0078,S0062,S0066B,S0003B 103976 300 MG SOLUTION FOR INJECTION /month
118663806 11866380 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0078,S0062,S0066B,S0003B 103976 300 MG SOLUTION FOR INJECTION /month
118663806 11866380 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0078,S0062,S0066B,S0003B 103976 SOLUTION FOR INJECTION
118663806 11866380 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0078,S0062,S0066B,S0003B 103976 SOLUTION FOR INJECTION
118663806 11866380 6 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0078,S0062,S0066B,S0003B 103976 300 MG SOLUTION FOR INJECTION
118663806 11866380 7 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0078,S0062,S0066B,S0003B 103976 600 MG SOLUTION FOR INJECTION
118663806 11866380 8 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0078,S0062,S0066B,S0003B 103976 300 MG SOLUTION FOR INJECTION
118663806 11866380 9 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown U 0
118663806 11866380 10 C SINGULAIR MONTELUKAST SODIUM 1 Unknown U 0
118663806 11866380 11 C NASACORT TRIAMCINOLONE ACETONIDE 1 Unknown U 0
118663806 11866380 12 C ATIVAN LORAZEPAM 1 0
118663806 11866380 13 C FOSAMAX ALENDRONATE SODIUM 1 Unknown U 0
118663806 11866380 14 C BRICANYL TERBUTALINE SULFATE 1 Unknown U 0
118663806 11866380 15 C DECADRON DEXAMETHASONE 1 Unknown U 0
118663806 11866380 16 C AMOXIL AMOXICILLIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118663806 11866380 1 Asthma
118663806 11866380 9 Product used for unknown indication
118663806 11866380 10 Product used for unknown indication
118663806 11866380 11 Product used for unknown indication
118663806 11866380 13 Product used for unknown indication
118663806 11866380 14 Product used for unknown indication
118663806 11866380 15 Product used for unknown indication
118663806 11866380 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118663806 11866380 HO
118663806 11866380 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118663806 11866380 Asthma
118663806 11866380 Cough
118663806 11866380 Dyspnoea exertional
118663806 11866380 Gastroenteritis
118663806 11866380 Incorrect dose administered
118663806 11866380 Influenza
118663806 11866380 Nasal congestion
118663806 11866380 Nasal discharge discolouration
118663806 11866380 Nasopharyngitis
118663806 11866380 Pain
118663806 11866380 Pruritus
118663806 11866380 Respiratory tract infection
118663806 11866380 Tooth infection
118663806 11866380 Urticaria
118663806 11866380 Vaginal infection
118663806 11866380 Wheezing

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
118663806 11866380 1 20060928 0
118663806 11866380 2 20090528 0
118663806 11866380 3 20100309 0
118663806 11866380 4 20160309 0
118663806 11866380 5 20160505 0
118663806 11866380 6 20160601 0
118663806 11866380 7 20160719 0
118663806 11866380 8 20160824 0