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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127802201 | 12780220 | 1 | I | 2016 | 20160921 | 20160926 | 20160926 | EXP | JP-ELI_LILLY_AND_COMPANY-JP201609007504 | ELI LILLY AND CO | 0.00 | M | Y | 0.00000 | 20160926 | CN | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127802201 | 12780220 | 1 | PS | HUMULIN 70/30 | INSULIN HUMAN | 1 | Subcutaneous | 8 IU, QD | U | U | 18780 | 8 | IU | INJECTION | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127802201 | 12780220 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127802201 | 12780220 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127802201 | 12780220 | Blood glucose increased | |
| 127802201 | 12780220 | Drug ineffective | |
| 127802201 | 12780220 | Expired device used | |
| 127802201 | 12780220 | Eye injury | |
| 127802201 | 12780220 | Hypoglycaemia | |
| 127802201 | 12780220 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |