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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123766474 | 12376647 | 4 | F | 2016 | 20160624 | 20160517 | 20160701 | EXP | GB-SA-2016SA093253 | AVENTIS | 37.00 | YR | A | F | Y | 0.00000 | 20160701 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123766474 | 12376647 | 1 | PS | LANTUS | INSULIN GLARGINE | 1 | Unknown | VIAL | U | A4775 | 21081 | SOLUTION FOR INJECTION | |||||||
| 123766474 | 12376647 | 2 | C | L-THYROXINE | LEVOTHYROXINE | 1 | 0 | 225 | UG | QD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123766474 | 12376647 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123766474 | 12376647 | Hospitalisation | |
| 123766474 | 12376647 | Hyperglycaemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |