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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125494211 | 12549421 | 1 | I | 2006 | 20160630 | 20160712 | 20160712 | EXP | BR-ELI_LILLY_AND_COMPANY-BR201607000104 | ELI LILLY AND CO | 0.00 | M | Y | 82.00000 | KG | 20160712 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125494211 | 12549421 | 1 | PS | HUMULIN N | INSULIN HUMAN | 1 | Subcutaneous | UNK, PRN | U | U | 18780 | ||||||||
| 125494211 | 12549421 | 2 | SS | HUMALOG | INSULIN LISPRO | 1 | Subcutaneous | 12 IU, QD | U | U | 0 | 12 | IU | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125494211 | 12549421 | 1 | Product used for unknown indication |
| 125494211 | 12549421 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125494211 | 12549421 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125494211 | 12549421 | Blood glucose increased | |
| 125494211 | 12549421 | Chronic kidney disease | |
| 125494211 | 12549421 | Drug dose omission |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |