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
127760181 12776018 1 I 20160730 20160916 20160923 20160923 EXP IT-ELI_LILLY_AND_COMPANY-IT201609006307 ELI LILLY AND CO 58.41 YR F Y 0.00000 20160923 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
127760181 12776018 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Oral 1 DF, UNKNOWN U U 21427 1 DF CAPSULE
127760181 12776018 2 C SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) UNK, UNKNOWN U 0 POWDER FOR ORAL SUSPENSION
127760181 12776018 3 C SAMYR /00882301/ ADEMETIONINE 1 Oral 1 DF, UNKNOWN U 0 1 DF TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127760181 12776018 1 Product used for unknown indication
127760181 12776018 2 Product used for unknown indication
127760181 12776018 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127760181 12776018 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127760181 12776018 Drug intolerance
127760181 12776018 Hyperhidrosis
127760181 12776018 Loss of consciousness
127760181 12776018 Nausea
127760181 12776018 Presyncope
127760181 12776018 Urinary incontinence

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
127760181 12776018 1 20160730 20160730 0