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
126486601 12648660 1 I 20120625 20160804 20160812 20160812 EXP US-ELI_LILLY_AND_COMPANY-US201608003483 ELI LILLY AND CO 48.89 YR F Y 0.00000 20160812 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
126486601 12648660 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U U 21427 CAPSULE
126486601 12648660 2 SS WELLBUTRIN BUPROPION HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U U 0
126486601 12648660 3 SS ASPIRIN /00002701/ ASPIRIN 1 Unknown UNK, UNKNOWN 0
126486601 12648660 4 SS PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126486601 12648660 1 Product used for unknown indication
126486601 12648660 2 Product used for unknown indication
126486601 12648660 3 Product used for unknown indication
126486601 12648660 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126486601 12648660 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126486601 12648660 Abdominal pain upper
126486601 12648660 Hypersensitivity
126486601 12648660 Rash
126486601 12648660 Suicidal ideation

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

no results found

Therapies reported

no results found