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
126664432 12666443 2 F 20160730 20160819 20160818 20160823 EXP US-ROCHE-1810286 ROCHE 36.82 YR F Y 68.10000 KG 20160823 MD US US

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
126664432 12666443 1 PS Pertuzumab PERTUZUMAB 1 Intravenous (not otherwise specified) U 125409 SOLUTION FOR INFUSION
126664432 12666443 2 SS Pertuzumab PERTUZUMAB 1 Intravenous (not otherwise specified) CYCLE 5 U 125409 420 MG SOLUTION FOR INFUSION Q3W
126664432 12666443 3 SS Trastuzumab TRASTUZUMAB 1 Intravenous (not otherwise specified) U 103792 136 MG SOLUTION FOR INFUSION /wk
126664432 12666443 4 SS NAB-PACLITAXEL PACLITAXEL 1 Intravenous (not otherwise specified) U 0 153 MG /wk
126664432 12666443 5 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126664432 12666443 1 HER-2 positive breast cancer
126664432 12666443 3 HER-2 positive breast cancer
126664432 12666443 4 HER-2 positive breast cancer

Outcome of event

Event ID CASEID OUTC COD
126664432 12666443 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126664432 12666443 Chest discomfort
126664432 12666443 Dyspnoea

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
126664432 12666443 2 20160715 0
126664432 12666443 3 20160729 0
126664432 12666443 4 20160729 0