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
1035639024 10356390 24 F 201403 20160815 20140801 20160822 EXP CA-ROCHE-1444303 ROCHE 70.67 YR M Y 87.00000 KG 20160822 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
1035639024 10356390 1 PS XOLAIR OMALIZUMAB 1 Subcutaneous 225 MG, BIW (EVERY 2 WEEKS) U S0059B,S0065E,S0068D 103976 225 MG SOLUTION FOR INJECTION QOW
1035639024 10356390 2 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 3 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 6 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 7 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 8 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 9 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 10 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 11 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 12 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 13 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 14 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 15 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 16 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 17 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 18 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 19 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 20 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 21 SS XOLAIR OMALIZUMAB 1 Subcutaneous U S0059B,S0065E,S0068D 103976 SOLUTION FOR INJECTION
1035639024 10356390 22 SS DIOVAN HCT HYDROCHLOROTHIAZIDEVALSARTAN 1 Unknown U 0
1035639024 10356390 23 C SINGULAIR MONTELUKAST SODIUM 1 Unknown U 0
1035639024 10356390 24 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown U 0
1035639024 10356390 25 C UNIPHYL THEOPHYLLINE ANHYDROUS 1 Unknown U 0
1035639024 10356390 26 C ALVESCO CICLESONIDE 1 Unknown U 0
1035639024 10356390 27 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Unknown U 0
1035639024 10356390 28 C VENTOLIN ALBUTEROL SULFATE 1 Unknown U 0
1035639024 10356390 29 C GUAIFENESIN. GUAIFENESIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1035639024 10356390 1 Asthma
1035639024 10356390 22 Hypertension
1035639024 10356390 23 Product used for unknown indication
1035639024 10356390 24 Product used for unknown indication
1035639024 10356390 25 Product used for unknown indication
1035639024 10356390 26 Product used for unknown indication
1035639024 10356390 27 Product used for unknown indication
1035639024 10356390 28 Product used for unknown indication
1035639024 10356390 29 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
1035639024 10356390 HO
1035639024 10356390 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1035639024 10356390 Abdominal pain upper
1035639024 10356390 Asthma
1035639024 10356390 Blood glucose abnormal
1035639024 10356390 Blood pressure increased
1035639024 10356390 Bronchitis
1035639024 10356390 Cough
1035639024 10356390 Influenza
1035639024 10356390 Peripheral swelling
1035639024 10356390 Pneumonia
1035639024 10356390 Road traffic accident
1035639024 10356390 Stress
1035639024 10356390 Throat irritation
1035639024 10356390 Weight decreased
1035639024 10356390 Weight increased

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
1035639024 10356390 1 20130807 0
1035639024 10356390 2 20140508 0
1035639024 10356390 3 20140522 0
1035639024 10356390 4 20140828 0
1035639024 10356390 5 20141030 0
1035639024 10356390 6 20141113 0
1035639024 10356390 7 20141211 0
1035639024 10356390 8 20150108 0
1035639024 10356390 9 20150219 0
1035639024 10356390 10 20150304 0
1035639024 10356390 11 20150416 0
1035639024 10356390 12 20151015 0
1035639024 10356390 13 20151112 0
1035639024 10356390 14 20151126 0
1035639024 10356390 15 20160331 0
1035639024 10356390 16 20160418 0
1035639024 10356390 17 20160519 0
1035639024 10356390 18 20160613 0
1035639024 10356390 19 20160630 0
1035639024 10356390 20 20160802 0
1035639024 10356390 21 20160815 0
1035639024 10356390 22 201408 0