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
119523393 11952339 3 F 20160901 20160126 20160902 EXP CA-ROCHE-1700114 ROCHE 73.00 YR F Y 0.00000 20160902 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
119523393 11952339 1 PS HERCEPTIN TRASTUZUMAB 1 Intravenous (not otherwise specified) THERAPY DURATION: 1 DAY U 103792 736 MG SOLUTION FOR INFUSION Q3W
119523393 11952339 2 SS HERCEPTIN TRASTUZUMAB 1 Intravenous (not otherwise specified) THERAPY DURATION: 1 DAY U 103792 552 MG SOLUTION FOR INFUSION Q3W
119523393 11952339 3 SS HERCEPTIN TRASTUZUMAB 1 Intravenous (not otherwise specified) THERAPY DURATION: 1 DAY U 103792 8 MG/KG SOLUTION FOR INFUSION Q3W
119523393 11952339 4 SS HERCEPTIN TRASTUZUMAB 1 Intravenous (not otherwise specified) THERAPY DURATION: 1 DAY U 103792 552 MG SOLUTION FOR INFUSION Q3W
119523393 11952339 5 SS PERJETA PERTUZUMAB 1 Intravenous (not otherwise specified) THERAPY DURATION: 1 DAY U 125409 840 MG Q3W
119523393 11952339 6 SS PERJETA PERTUZUMAB 1 Intravenous (not otherwise specified) THERAPY DURATION: 1 DAY U 125409 420 MG Q3W
119523393 11952339 7 SS PERJETA PERTUZUMAB 1 Intravenous (not otherwise specified) U 125409 420 MG Q3W
119523393 11952339 8 SS PERJETA PERTUZUMAB 1 Intravenous (not otherwise specified) THERAPY DURATION: 1 DAY U 125409 420 MG Q3W
119523393 11952339 9 SS CARBOPLATIN. CARBOPLATIN 1 Intravenous (not otherwise specified) THERAPY DURATION: 1 DAY U 0 476 MG Q3W
119523393 11952339 10 SS CARBOPLATIN. CARBOPLATIN 1 Intravenous (not otherwise specified) THERAPY DURATION: 1 DAY U 0 694 MG Q3W
119523393 11952339 11 SS CARBOPLATIN. CARBOPLATIN 1 Intravenous (not otherwise specified) THERAPY DURATION: 1 DAY U 0 476 MG Q3W
119523393 11952339 12 SS DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) U 0 Q3W
119523393 11952339 13 SS DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) U 0 119 MG Q3W
119523393 11952339 14 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Unknown 0
119523393 11952339 15 C COVERSYL PERINDOPRIL 1 0
119523393 11952339 16 C DECADRON DEXAMETHASONE 1 Unknown 0
119523393 11952339 17 C KYTRIL GRANISETRON HYDROCHLORIDE 1 Unknown 0
119523393 11952339 18 C METFORMIN METFORMIN HYDROCHLORIDE 1 0
119523393 11952339 19 C ANCEF CEFAZOLIN SODIUM 1 Unknown 0
119523393 11952339 20 C CEFADROXIL. CEFADROXIL 1 0
119523393 11952339 21 C GRAVOL DIMENHYDRINATE 1 0
119523393 11952339 22 C HEPARIN SODIUM. HEPARIN SODIUM 1 Unknown 0
119523393 11952339 23 C HUMULIN R INSULIN HUMAN 1 0
119523393 11952339 24 C K-DUR POTASSIUM CHLORIDE 1 0
119523393 11952339 25 C MAGNESIUM GLUCEPTATE MAGNESIUM GLUCEPTATE 1 Oral 0
119523393 11952339 26 C MAGNESIUM GLUCONATE MAGNESIUM GLUCONATE 1 0
119523393 11952339 27 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 0
119523393 11952339 28 C POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 0
119523393 11952339 29 C SODIUM BICARBONATE. SODIUM BICARBONATE 1 0
119523393 11952339 30 C ROSUVASTATIN. ROSUVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119523393 11952339 1 Breast cancer
119523393 11952339 5 Breast cancer
119523393 11952339 9 Breast cancer
119523393 11952339 12 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
119523393 11952339 LT
119523393 11952339 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119523393 11952339 Cellulitis
119523393 11952339 Clostridium difficile infection
119523393 11952339 Diarrhoea
119523393 11952339 Enterocolitis infectious

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found