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
108421907 10842190 7 F 20150128 20160705 20150220 20160707 EXP DE-ROCHE-1540490 ROCHE 65.00 YR F Y 86.50000 KG 20160707 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
108421907 10842190 1 PS Trastuzumab TRASTUZUMAB 1 Subcutaneous B0031,B1006 103792 600 MG Q3W
108421907 10842190 2 SS Trastuzumab TRASTUZUMAB 1 Subcutaneous B0031,B1006 103792 600 MG Q3W
108421907 10842190 3 SS DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) 0 75 MG/M**2 QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108421907 10842190 1 Breast cancer
108421907 10842190 3 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
108421907 10842190 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
108421907 10842190 Dizziness
108421907 10842190 Gastroenteritis
108421907 10842190 Hypertensive crisis
108421907 10842190 Palpitations
108421907 10842190 Panic attack
108421907 10842190 Pyrexia
108421907 10842190 Restlessness

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
108421907 10842190 1 20140520 20141202 0
108421907 10842190 2 20150115 20150511 0
108421907 10842190 3 20140519 20140915 0