The Safety Rates Drug Report

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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
125724071 12572407 1 I 20160707 20160708 20160719 20160719 PER US-ELI_LILLY_AND_COMPANY-US201607003881 ELI LILLY AND CO 25.11 YR M Y 0.00000 20160719 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
125724071 12572407 1 PS HUMALOG INSULIN LISPRO 1 Unknown UNK, UNKNOWN 20563 INJECTION
125724071 12572407 2 SS HUMALOG INSULIN LISPRO 1 Unknown UNK, UNKNOWN C292707A 20563 INJECTION
125724071 12572407 3 C LANTUS INSULIN GLARGINE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125724071 12572407 1 Type 1 diabetes mellitus
125724071 12572407 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125724071 12572407 Anxiety
125724071 12572407 Hyperhidrosis
125724071 12572407 Incorrect product storage
125724071 12572407 Insomnia
125724071 12572407 Nervousness
125724071 12572407 Stress

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
125724071 12572407 1 1999 0