The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
8623744 8556691 F 8623744-4 20120425 20120817 20120827 EXP DE-TEVA-336755GER TEVA 57 YR F Y 72 KG 20120827 MD GERMANY

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
8623744 1020671040 SS LAPATINIB 1 ORAL 750 MILLIGRAM DAILY;
8623744 1020671041 SS TRASTUZUMAB 2 INTRAVENOUS H4059B01
8623744 1020671036 PS PACLITAXEL 1 Y036843AB 075297
8623744 1020671042 C GRANOCYTE 2
8623744 1020671034 SS DOXORUBICIN HYDROCHLORIDE 1 INTRAVENOUS 11G11DE
8623744 1020671039 SS CARBOPLATIN 1 INTRAVENOUS Y121686AA
8623744 1020671038 SS CARBOPLATIN 1 Y121686AA
8623744 1020671035 SS DOXORUBICIN HYDROCHLORIDE 1 INTRAVENOUS 4.7143 MILLIGRAM DAILY; 11G11DE
8623744 1020671037 SS PACLITAXEL 1 INTRAVENOUS 11.4286 MG/M2 DAILY; Y036843AB 075297
8623744 1020671043 C CIPROFLOXACIN HCL 1 1000 MILLIGRAM DAILY;

Indications of drugs used

Event ID DRUG SEQ INDI PT
8623744 1020671040 BREAST CANCER
8623744 1020671041 BREAST CANCER
8623744 1020671036 BREAST CANCER
8623744 1020671034 BREAST CANCER
8623744 1020671038 BREAST CANCER

Outcome of event

Event ID OUTC COD
8623744 HO

Reactions reported

Event ID PT
8623744 STOMATITIS

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
8623744 1020671040 20120315
8623744 1020671041 20120315 20120425
8623744 1020671036 20120315 20120502 47 DAY
8623744 1020671042 20120426 20120429
8623744 1020671034 20120315 20120502 47 DAY
8623744 1020671039 20120516 47 DAY
8623744 1020671038 20120315 20120502 47 DAY
8623744 1020671035 20120516 47 DAY
8623744 1020671037 20120516 47 DAY
8623744 1020671043 20120419 20120420