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
125695301 12569530 1 I 20160707 0 20160718 20160718 DIR 24.35 YR M N 85.00000 KG 20160715 N MD 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
125695301 12569530 1 PS CARBOPLATIN. CARBOPLATIN 1 0 3300 MG
125695301 12569530 2 SS ETOPOSIDE (VP-16) ETOPOSIDE 1 0 2400 MG
125695301 12569530 3 SS IFOSFAMIDE. IFOSFAMIDE 1 0
125695301 12569530 4 SS TAXOL PACLITAXEL 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125695301 12569530 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125695301 12569530 Colitis
125695301 12569530 Enteritis
125695301 12569530 Febrile neutropenia
125695301 12569530 Haemoglobin decreased
125695301 12569530 Platelet count decreased

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

Event ID CASEID RPSR COD
125695301 12569530 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125695301 12569530 1 20160629 0
125695301 12569530 2 20160629 0
125695301 12569530 3 20160522 0
125695301 12569530 4 20160520 0