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
125656901 12565690 1 I 20120418 20121025 20160718 20160718 EXP GB-PFIZER INC-1470995 PFIZER 59.00 YR M Y 79.00000 KG 20160718 OT AU AU

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
125656901 12565690 1 PS CALCIUM FOLINATE LEUCOVORIN CALCIUM 1 Intravenous (not otherwise specified) 790 MG, FREQ: 2 WEEK; INTERVAL: 1 UNK 8107 790 MG
125656901 12565690 2 SS FLUOROURACIL. FLUOROURACIL 1 Intravenous bolus 790/473 MG, EVERY 2 WEEKS, 2/52 U UNK 0
125656901 12565690 3 SS IRINOTECAN HCL IRINOTECAN HYDROCHLORIDE 1 Intravenous (not otherwise specified) 355 MG, FREQ: 2 WEEK; INTERVAL: 1 U UNK 20571 355 MG
125656901 12565690 4 C PANADOL /00020001/ 2 1 G, UNK 0 1 G

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125656901 12565690 1 Colon cancer
125656901 12565690 2 Colon cancer
125656901 12565690 3 Colon cancer
125656901 12565690 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125656901 12565690 OT
125656901 12565690 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125656901 12565690 Febrile neutropenia

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
125656901 12565690 1 20120131 0
125656901 12565690 2 20120131 0
125656901 12565690 3 20120131 0