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
114419924 11441992 4 F 20140817 20160815 20150901 20160818 EXP JP-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-056579 ELI LILLY AND CO 66.00 YR M Y 0.00000 20160818 CN DE 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
114419924 11441992 1 PS CETUXIMAB CETUXIMAB 1 Intravenous (not otherwise specified) UNK UNK, UNKNOWN U 125084
114419924 11441992 2 SS CISPLATIN. CISPLATIN 1 Intravenous (not otherwise specified) UNK UNK, UNKNOWN U U 0
114419924 11441992 3 SS 5 FU FLUOROURACIL 1 Intravenous (not otherwise specified) UNK UNK, UNKNOWN U U 0
114419924 11441992 4 SS MONILAC LACTULOSE 1 Oral UNK UNK, UNKNOWN U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114419924 11441992 1 Squamous cell carcinoma of head and neck
114419924 11441992 2 Squamous cell carcinoma of head and neck
114419924 11441992 3 Squamous cell carcinoma of head and neck
114419924 11441992 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
114419924 11441992 LT
114419924 11441992 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114419924 11441992 Blood alkaline phosphatase increased
114419924 11441992 Decreased appetite
114419924 11441992 Dermatitis acneiform
114419924 11441992 Diarrhoea
114419924 11441992 Hypokalaemia
114419924 11441992 Hyponatraemia
114419924 11441992 Nausea
114419924 11441992 Neutrophil count decreased
114419924 11441992 Platelet count decreased
114419924 11441992 White blood cell count decreased

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
114419924 11441992 1 20140815 0