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
117969222 11796922 2 F 201604 20160706 20151203 20160708 PER US-ELI_LILLY_AND_COMPANY-US201511009747 ELI LILLY AND CO 0.00 F Y 0.00000 20160708 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
117969222 11796922 1 PS HUMALOG INSULIN LISPRO 1 Unknown UNK 20563 INJECTION
117969222 11796922 2 SS HUMALOG INSULIN LISPRO 1 Unknown UNK 20563 INJECTION
117969222 11796922 3 SS HUMALOG INSULIN LISPRO 1 Unknown UNK UNK, UNKNOWN 20563 INJECTION
117969222 11796922 4 SS HUMALOG INSULIN LISPRO 1 Unknown 25 U, TID (20 TO 25 UNITS) C522514E 20563 25 IU INJECTION TID
117969222 11796922 5 C LANTUS INSULIN GLARGINE 1 Unknown UNK, UNKNOWN U 0
117969222 11796922 6 C TOUJEO INSULIN GLARGINE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117969222 11796922 1 Product used for unknown indication
117969222 11796922 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
117969222 11796922 Blood glucose increased
117969222 11796922 Hypoacusis
117969222 11796922 Incorrect dose administered
117969222 11796922 Injection site haemorrhage

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
117969222 11796922 2 20151123 0
117969222 11796922 4 201604 0