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
126799872 12679987 2 F 201001 20160828 20160824 20160908 EXP HU-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-122697 RANBAXY 24.00 YR F Y 0.00000 20160908 OT GB HU

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
126799872 12679987 1 PS CARBOPLATIN. CARBOPLATIN 1 Unknown UNK Y 77926
126799872 12679987 2 SS ETOPOSIDE. ETOPOSIDE 1 Unknown UNK Y 0
126799872 12679987 3 SS IFOSFAMIDE. IFOSFAMIDE 1 Unknown UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126799872 12679987 1 Disease progression
126799872 12679987 2 Disease progression
126799872 12679987 3 Disease progression

Outcome of event

Event ID CASEID OUTC COD
126799872 12679987 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126799872 12679987 Bone marrow failure
126799872 12679987 Drug intolerance

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
126799872 12679987 1 20100107 20100111 0
126799872 12679987 2 20100107 20100111 0
126799872 12679987 3 20100107 20100111 0