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
100084992 10008499 2 F 20140325 20140313 20140331 EXP JP-ELI_LILLY_AND_COMPANY-JP201403001486 ELI LILLY AND CO 65.00 YR M Y 0.00000 20140330 N CN 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
100084992 10008499 1 PS Gemcitabine Hydrochloride 1 INTRAVENOUS 1000 MG/M2, UNK D 20509 1000 MG/M**2
100084992 10008499 2 C CISPLATIN 1 INTRAVENOUS 36 MG/M2, UNK D 0 36 MG/M**2
100084992 10008499 3 C TS 1 1 UNKNOWN 100 MG, UNK D 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100084992 10008499 1 Gallbladder cancer stage IV
100084992 10008499 2 Gallbladder cancer stage IV
100084992 10008499 3 Gallbladder cancer stage IV

Outcome of event

Event ID CASEID OUTC COD
100084992 10008499 OT
100084992 10008499 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100084992 10008499 Decreased appetite
100084992 10008499 Hypercalcaemia
100084992 10008499 Leukocytosis
100084992 10008499 Pulmonary embolism

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

no results found

Therapies reported

no results found