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
125844423 12584442 3 F 20160802 20160722 20160817 EXP JP-SA-2016SA129665 AVENTIS 0.00 E M Y 0.00000 20160817 OT JP JP

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
125844423 12584442 1 PS TAXOTERE DOCETAXEL 1 Unknown U UNKNOWN 20449 75 MG/M**2 /cycle
125844423 12584442 2 SS CISPLATIN. CISPLATIN 1 Unknown U UNKNOWN 0 75 MG/M**2 /cycle
125844423 12584442 3 SS 5-FU FLUOROURACIL 1 Unknown U UNKNOWN 0 750 MG/M**2 /cycle

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125844423 12584442 1 Oesophageal carcinoma
125844423 12584442 2 Oesophageal carcinoma
125844423 12584442 3 Oesophageal carcinoma

Outcome of event

Event ID CASEID OUTC COD
125844423 12584442 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125844423 12584442 Altered state of consciousness
125844423 12584442 Hyperammonaemic encephalopathy
125844423 12584442 Neutrophil count decreased

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

no results found

Therapies reported

no results found