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
126866711 12686671 1 I 20160818 20160825 20160825 EXP CA-ELI_LILLY_AND_COMPANY-CA201608009405 ELI LILLY AND CO 64.00 YR F Y 0.00000 20160825 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
126866711 12686671 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U U 21427 CAPSULE
126866711 12686671 2 SS HYDROMORPHONE HYDROMORPHONE 1 Unknown UNK, UNKNOWN U U 0
126866711 12686671 3 SS LYRICA PREGABALIN 1 Unknown UNK, UNKNOWN U U 0
126866711 12686671 4 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, BID U U 0 5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126866711 12686671 1 Product used for unknown indication
126866711 12686671 2 Product used for unknown indication
126866711 12686671 3 Product used for unknown indication
126866711 12686671 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126866711 12686671 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126866711 12686671 Condition aggravated
126866711 12686671 Costochondritis
126866711 12686671 Fatigue
126866711 12686671 Hypersomnia
126866711 12686671 Rheumatoid arthritis

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

no results found

Therapies reported

no results found