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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124617665 | 12461766 | 5 | F | 2016 | 20160727 | 20160613 | 20160808 | EXP | US-SA-2016SA104991 | AVENTIS | 80.00 | YR | E | F | Y | 0.00000 | 20160808 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124617665 | 12461766 | 1 | PS | LANTUS | INSULIN GLARGINE | 1 | Unknown | DOSE:10 UNIT(S) | 5F452A | 21081 | SOLUTION FOR INJECTION | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124617665 | 12461766 | 1 | Diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124617665 | 12461766 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124617665 | 12461766 | Blood pressure increased | |
| 124617665 | 12461766 | Dizziness | |
| 124617665 | 12461766 | Fatigue | |
| 124617665 | 12461766 | Feeling hot | |
| 124617665 | 12461766 | Gait disturbance | |
| 124617665 | 12461766 | Heart rate decreased | |
| 124617665 | 12461766 | Hypersomnia | |
| 124617665 | 12461766 | Injection site pain | |
| 124617665 | 12461766 | Malaise | |
| 124617665 | 12461766 | Unevaluable event | |
| 124617665 | 12461766 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |