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
112388298 11238829 8 F 20131105 20160802 20150706 20160805 EXP CA-ROCHE-1603761 ROCHE 57.62 YR M Y 0.00000 20160805 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
112388298 11238829 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous 375 MG, BIW U S00062,S0002F 103976 375 MG SOLUTION FOR INJECTION QOW
112388298 11238829 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous 375 MG, BIW U S00062,S0002F 103976 375 MG SOLUTION FOR INJECTION QOW
112388298 11238829 6 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 7 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 8 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 9 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 10 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 11 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 12 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 13 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 14 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 15 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 16 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S00062,S0002F 103976 SOLUTION FOR INJECTION
112388298 11238829 17 C VENTOLIN ALBUTEROL SULFATE 1 0
112388298 11238829 18 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0
112388298 11238829 19 C ZENHALE FORMOTEROL FUMARATEMOMETASONE FUROATE 1 0
112388298 11238829 20 C SINGULAIR MONTELUKAST SODIUM 1 0
112388298 11238829 21 C CRESTOR ROSUVASTATIN CALCIUM 1 0
112388298 11238829 22 C NORVASC AMLODIPINE BESYLATE 1 0
112388298 11238829 23 C ATIVAN LORAZEPAM 1 0
112388298 11238829 24 C TRAZODONE TRAZODONE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112388298 11238829 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
112388298 11238829 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112388298 11238829 Blood pressure increased
112388298 11238829 Oxygen saturation decreased
112388298 11238829 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
112388298 11238829 1 20130716 0
112388298 11238829 2 20131105 0
112388298 11238829 3 20131203 0
112388298 11238829 4 20141014 0
112388298 11238829 5 20141028 0
112388298 11238829 6 20141125 0
112388298 11238829 7 20150120 0
112388298 11238829 8 20150623 0
112388298 11238829 9 20150915 0
112388298 11238829 10 20151027 0
112388298 11238829 11 20151124 0
112388298 11238829 12 20160105 0
112388298 11238829 13 20160119 0
112388298 11238829 14 20160301 0
112388298 11238829 15 20160719 0
112388298 11238829 16 20160802 0