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
1132564810 11325648 10 F 20150611 20160830 20150731 20160902 EXP DE-ROCHE-1615088 ROCHE 0.00 A F Y 57.00000 KG 20160902 MD DE DE

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
1132564810 11325648 1 PS Trastuzumab TRASTUZUMAB 1 Subcutaneous U 103792 600 MG SOLUTION FOR INJECTION Q3W
1132564810 11325648 2 SS TAMOXIFEN TAMOXIFEN 1 Oral U 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1132564810 11325648 1 Breast cancer
1132564810 11325648 2 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
1132564810 11325648 OT
1132564810 11325648 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
1132564810 11325648 Chills
1132564810 11325648 Hot flush
1132564810 11325648 Impaired healing
1132564810 11325648 Injection site pain
1132564810 11325648 Injection site pruritus
1132564810 11325648 Pyrexia
1132564810 11325648 Vomiting
1132564810 11325648 Weight increased
1132564810 11325648 Wound infection

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
1132564810 11325648 1 20150414 20151110 0
1132564810 11325648 2 20150527 0