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
125226501 12522650 1 I 20160620 20160701 20160701 EXP BR-ELI_LILLY_AND_COMPANY-BR201606008255 ELI LILLY AND CO 0.00 M Y 54.50000 KG 20160701 CN BR BR

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
125226501 12522650 1 PS HUMALOG INSULIN LISPRO 1 Subcutaneous UNK UNK, UNKNOWN U 20563 INJECTION
125226501 12522650 2 SS HUMALOG INSULIN LISPRO 1 Subcutaneous UNK UNK, UNKNOWN U C433518E 20563 INJECTION
125226501 12522650 3 C HYDROCORTISONE. HYDROCORTISONE 1 Unknown UNK, UNKNOWN U 0
125226501 12522650 4 C NORTRIPTYLINE NORTRIPTYLINE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125226501 12522650 1 Type 1 diabetes mellitus
125226501 12522650 3 Adrenal disorder

Outcome of event

Event ID CASEID OUTC COD
125226501 12522650 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125226501 12522650 Adrenal disorder
125226501 12522650 Blood glucose increased
125226501 12522650 Drug ineffective
125226501 12522650 Fatigue
125226501 12522650 Feeling abnormal
125226501 12522650 Incorrect product storage
125226501 12522650 Irritability
125226501 12522650 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
125226501 12522650 1 2013 20160620 0