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
127839141 12783914 1 I 20160919 20160927 20160927 EXP US-ELI_LILLY_AND_COMPANY-US201609007393 ELI LILLY AND CO 0.00 F Y 0.00000 20160926 CN 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
127839141 12783914 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown UNK UNK, UNKNOWN U U 21427 CAPSULE
127839141 12783914 2 SS LYRICA PREGABALIN 1 Unknown 100 MG, TID Y U N17614 0 100 MG TID
127839141 12783914 3 C COREG CARVEDILOL 1 Unknown UNK, UNKNOWN U 0
127839141 12783914 4 C TRAMADOL. TRAMADOL 1 Unknown UNK, UNKNOWN U 0
127839141 12783914 5 C FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0
127839141 12783914 6 C MOBIC MELOXICAM 1 Unknown UNK, UNKNOWN U 0
127839141 12783914 7 C HORIZANT GABAPENTIN ENACARBIL 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127839141 12783914 1 Product used for unknown indication
127839141 12783914 2 Back pain

Outcome of event

Event ID CASEID OUTC COD
127839141 12783914 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127839141 12783914 Dizziness
127839141 12783914 Fatigue
127839141 12783914 Oropharyngeal pain
127839141 12783914 Sinus congestion
127839141 12783914 Somnolence

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
127839141 12783914 2 201604 0