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
124224722 12422472 2 F 20160521 20160629 20160601 20160706 EXP PL-AMGEN-POLSP2016067743 AMGEN 65.00 YR E F Y 60.00000 KG 20160706 MD PL PL

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
124224722 12422472 1 PS NEULASTA PEGFILGRASTIM 1 Subcutaneous 60 MG, UNK Y 125031 60 MG UNKNOWN FORMULATION
124224722 12422472 2 C TAMOXIFEN TAMOXIFEN 1 UNK 0
124224722 12422472 3 C TAMOXIFEN TAMOXIFEN 1 0
124224722 12422472 4 C TAXOTERE DOCETAXEL 1 UNK 0
124224722 12422472 5 C DOXORUBICIN DOXORUBICIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124224722 12422472 1 Prophylaxis
124224722 12422472 2 Breast cancer
124224722 12422472 3 Metastases to lung

Outcome of event

Event ID CASEID OUTC COD
124224722 12422472 OT
124224722 12422472 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124224722 12422472 Dehydration
124224722 12422472 Diarrhoea
124224722 12422472 Drug ineffective
124224722 12422472 Febrile neutropenia

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
124224722 12422472 1 20160515 20160515 0