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
8480346 8644647 I 8480346-0 20120616 20120620 20120630 EXP DE-TEVA-345230GER TEVA 51 YR F Y 96 KG 20120630 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
8480346 1020135298 SS PACLITAXEL 1 INTRAVENOUS
8480346 1020135302 C ALIZAPRIDE 2
8480346 1020135300 SS AVASTIN 1 INTRAVENOUS
8480346 1020135303 C CLEMASTINE 2 2 MILLIGRAM;
8480346 1020135304 C RANITIDINE HCL 1
8480346 1020135297 SS DOXORUBICIN HCL 1 INTRAVENOUS
8480346 1020135299 PS CARBOPLATIN 1 INTRAVENOUS 077269
8480346 1020135301 SS DEXAMETHASONE 1 12 MILLIGRAM; 081125

Indications of drugs used

Event ID DRUG SEQ INDI PT
8480346 1020135298 BREAST CANCER
8480346 1020135302 PREMEDICATION
8480346 1020135300 BREAST CANCER
8480346 1020135303 PREMEDICATION
8480346 1020135304 PREMEDICATION
8480346 1020135297 BREAST CANCER
8480346 1020135299 BREAST CANCER
8480346 1020135301 PREMEDICATION

Outcome of event

Event ID OUTC COD
8480346 HO

Reactions reported

Event ID PT
8480346 THROMBOSIS

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
8480346 1020135302 20120402
8480346 1020135303 20120402
8480346 1020135304 20120402
8480346 1020135297 20120402
8480346 1020135299 20120402
8480346 1020135301 20120402