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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126081091 | 12608109 | 1 | I | 20160129 | 20160721 | 20160729 | 20160729 | EXP | IT-SA-2016SA134543 | AVENTIS | 33.00 | YR | A | M | Y | 0.00000 | 20160729 | MD | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126081091 | 12608109 | 1 | PS | LANTUS | INSULIN GLARGINE | 1 | Subcutaneous | U | UNK | 21081 | 27 | IU | QD | ||||||
| 126081091 | 12608109 | 2 | SS | NOVORAPID | INSULIN ASPART | 1 | Subcutaneous | U | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126081091 | 12608109 | 1 | Type 1 diabetes mellitus |
| 126081091 | 12608109 | 2 | Type 1 diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126081091 | 12608109 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126081091 | 12608109 | Feeling jittery | |
| 126081091 | 12608109 | Hypoglycaemia | |
| 126081091 | 12608109 | Malaise |
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 |
|---|---|---|---|---|---|---|
| 126081091 | 12608109 | 1 | 20150101 | 20160128 | 0 | |
| 126081091 | 12608109 | 2 | 20150101 | 20160129 | 0 |