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
126585841 12658584 1 I 20160412 0 20160816 20160816 DIR 68.00 YR M N 88.50000 KG 20160722 N PH 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
126585841 12658584 1 PS CISPLATIN. CISPLATIN 1 Intravenous (not otherwise specified) D N 0 200 MG 1X
126585841 12658584 2 SS DOXORUBICIN DOXORUBICIN 1 Intravenous (not otherwise specified) D N 0 50 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126585841 12658584 1 Osteosarcoma
126585841 12658584 2 Osteosarcoma

Outcome of event

Event ID CASEID OUTC COD
126585841 12658584 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126585841 12658584 Dysphagia
126585841 12658584 Mucosal inflammation
126585841 12658584 Neutropenia
126585841 12658584 Pain

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

Event ID CASEID RPSR COD
126585841 12658584 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126585841 12658584 1 20160330 20160330 0
126585841 12658584 2 20160330 20160404 0