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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125208661 | 12520866 | 1 | I | 20160620 | 20160701 | 20160701 | EXP | US-SA-2016SA116434 | AVENTIS | 63.00 | YR | A | F | Y | 0.00000 | 20160701 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125208661 | 12520866 | 1 | PS | TOUJEO | INSULIN GLARGINE | 1 | Unknown | DOSE:40 UNIT(S) | UNKNOWN | 206538 | INJECTION | QD | |||||||
| 125208661 | 12520866 | 2 | SS | TOUJEO | INSULIN GLARGINE | 1 | Unknown | DOSE:10 UNIT(S) | UNKNOWN | 206538 | INJECTION | QD | |||||||
| 125208661 | 12520866 | 3 | SS | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 125208661 | 12520866 | 4 | C | SOLOSTAR | DEVICE | 1 | 0 | ||||||||||||
| 125208661 | 12520866 | 5 | C | SOLOSTAR | DEVICE | 1 | 0 | ||||||||||||
| 125208661 | 12520866 | 6 | C | AMIODARONE | AMIODARONE | 1 | 0 | ||||||||||||
| 125208661 | 12520866 | 7 | C | MULTAQ | DRONEDARONE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125208661 | 12520866 | 1 | Type 2 diabetes mellitus |
| 125208661 | 12520866 | 2 | Type 2 diabetes mellitus |
| 125208661 | 12520866 | 3 | Type 2 diabetes mellitus |
| 125208661 | 12520866 | 4 | Type 2 diabetes mellitus |
| 125208661 | 12520866 | 5 | Type 2 diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125208661 | 12520866 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125208661 | 12520866 | Atrial fibrillation | |
| 125208661 | 12520866 | Blood glucose increased | |
| 125208661 | 12520866 | Dehydration | |
| 125208661 | 12520866 | Diarrhoea | |
| 125208661 | 12520866 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |