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
127253421 12725342 1 I 201607 20160901 20160908 20160908 EXP JP-ELI_LILLY_AND_COMPANY-JP201609001501 ELI LILLY AND CO 65.00 YR M Y 0.00000 20160908 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
127253421 12725342 1 PS CYRAMZA RAMUCIRUMAB 1 Intravenous (not otherwise specified) 8 MG/KG, OTHER Y U 125477 8 MG/KG INJECTION
127253421 12725342 2 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127253421 12725342 1 Gastric cancer
127253421 12725342 2 Gastric cancer

Outcome of event

Event ID CASEID OUTC COD
127253421 12725342 HO
127253421 12725342 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127253421 12725342 Anaemia
127253421 12725342 Bone marrow failure
127253421 12725342 Jaundice
127253421 12725342 Malignant neoplasm progression
127253421 12725342 Platelet count decreased
127253421 12725342 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
127253421 12725342 1 201512 201607 0
127253421 12725342 2 201512 0