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
125492151 12549215 1 I 20160704 20160712 20160712 EXP IT-ELI_LILLY_AND_COMPANY-IT201607001258 ELI LILLY AND CO 0.00 A F Y 0.00000 20160711 CN IT IT

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
125492151 12549215 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 21427 CAPSULE
125492151 12549215 2 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 30 MG, UNKNOWN U C599849 21427 30 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125492151 12549215 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125492151 12549215 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125492151 12549215 Abdominal pain upper
125492151 12549215 Breath odour
125492151 12549215 Confusional state
125492151 12549215 Constipation
125492151 12549215 Diarrhoea
125492151 12549215 Dizziness
125492151 12549215 Eating disorder
125492151 12549215 Eructation
125492151 12549215 Hyperhidrosis
125492151 12549215 Malaise
125492151 12549215 Mouth swelling
125492151 12549215 Nausea
125492151 12549215 Paraesthesia
125492151 12549215 Paraesthesia oral
125492151 12549215 Peripheral swelling
125492151 12549215 Pyrexia
125492151 12549215 Somnolence
125492151 12549215 Swelling face
125492151 12549215 Tremor
125492151 12549215 Vision blurred

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
125492151 12549215 2 20160628 20160702 0