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
127869521 12786952 1 I 20160408 20160922 20160928 20160928 EXP GB-ELI_LILLY_AND_COMPANY-GB201609008093 ELI LILLY AND CO 59.00 YR M Y 133.00000 KG 20160928 CN GB GB

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
127869521 12786952 1 PS Insulin Human INSULIN HUMAN 1 Unknown UNK UNK, UNKNOWN U U 18780
127869521 12786952 2 SS LYXUMIA LIXISENATIDE 1 Subcutaneous 10 UG, QD 359.583 UG U U UNK 0 10 UG QD
127869521 12786952 3 SS TOUJEO INSULIN GLARGINE 1 Unknown UNK UNK, UNKNOWN U U UNKNOWN 0
127869521 12786952 4 C MORPHINE MORPHINE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127869521 12786952 1 Product used for unknown indication
127869521 12786952 2 Type 2 diabetes mellitus
127869521 12786952 3 Product used for unknown indication
127869521 12786952 4 Abdominal pain upper

Outcome of event

Event ID CASEID OUTC COD
127869521 12786952 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127869521 12786952 Death

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
127869521 12786952 2 20160303 0
127869521 12786952 3 20160105 0