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
126097651 12609765 1 I 20160720 20160801 20160801 EXP US-CIPLA LTD.-2016US10109 CIPLA 0.00 Y 0.00000 20160801 OT US US

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
126097651 12609765 1 PS Irinotecan IRINOTECAN 1 Unknown 65 MG/M2 ON WEEKS 1, 2, 4, AND 5 U 77219 65 MG/M**2
126097651 12609765 2 SS CELECOXIB. CELECOXIB 1 Oral 400 MG, BID, 3 DAYS PRIOR TO CHEMOTHERAPY AND STOPPED 1 WEEK BEFORE SURGERY U 0 400 MG BID
126097651 12609765 3 SS CISPLATIN. CISPLATIN 1 Intravenous (not otherwise specified) 30 MG/M2 ON WEEKS 1, 2, 4, AND 5 U 0 30 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126097651 12609765 1 Oesophageal carcinoma
126097651 12609765 2 Oesophageal carcinoma
126097651 12609765 3 Oesophageal carcinoma

Outcome of event

Event ID CASEID OUTC COD
126097651 12609765 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126097651 12609765 Febrile neutropenia
126097651 12609765 Sepsis

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

no results found

Therapies reported

no results found