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
125776012 12577601 2 F 20160518 20160819 20160720 20160831 EXP CA-ELI_LILLY_AND_COMPANY-CA201606009895 ELI LILLY AND CO 66.00 YR F Y 0.00000 20160831 CN CA CA

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
125776012 12577601 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 30 MG, UNKNOWN U C563371 21427 30 MG CAPSULE QD
125776012 12577601 2 C MULTI VITAMIN VITAMINS 1 Unknown UNK, UNKNOWN 0
125776012 12577601 3 C ASCORBIC ACID. ASCORBIC ACID 1 Unknown UNK, UNKNOWN 0
125776012 12577601 4 C COBALAMIN COBALAMIN 1 Unknown UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125776012 12577601 1 Pain

Outcome of event

Event ID CASEID OUTC COD
125776012 12577601 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125776012 12577601 Dysgeusia
125776012 12577601 Gastrointestinal stromal tumour
125776012 12577601 Nausea
125776012 12577601 Somnolence
125776012 12577601 Ultrasound abdomen abnormal
125776012 12577601 Vomiting

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
125776012 12577601 1 20160516 0