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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124213372 | 12421337 | 2 | F | 20160409 | 20160713 | 20160531 | 20160721 | EXP | US-SA-2016SA101362 | AVENTIS | 79.00 | YR | E | F | Y | 0.00000 | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124213372 | 12421337 | 1 | PS | LANTUS SOLOSTAR | INSULIN GLARGINE | 1 | Unknown | DOSE:35 UNIT(S) | 6F2925A | 21081 | QD | ||||||||
| 124213372 | 12421337 | 2 | SS | LANTUS SOLOSTAR | INSULIN GLARGINE | 1 | Unknown | DOSE:35 UNIT(S) | UNK | 21081 | QD | ||||||||
| 124213372 | 12421337 | 3 | C | SOLOSTAR | DEVICE | 1 | 6F2925A | 0 | |||||||||||
| 124213372 | 12421337 | 4 | C | LISINOPRIL. | LISINOPRIL | 1 | 0 | 20 | MG | QD | |||||||||
| 124213372 | 12421337 | 5 | C | ATORVASTATIN | ATORVASTATIN | 1 | 0 | 20 | MG | QD | |||||||||
| 124213372 | 12421337 | 6 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | 0 | 10 | MG | QD | |||||||||
| 124213372 | 12421337 | 7 | C | ASPIRIN. | ASPIRIN | 1 | 0 | 81 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124213372 | 12421337 | 1 | Type 2 diabetes mellitus |
| 124213372 | 12421337 | 2 | Type 2 diabetes mellitus |
| 124213372 | 12421337 | 3 | Type 2 diabetes mellitus |
| 124213372 | 12421337 | 4 | Blood pressure increased |
| 124213372 | 12421337 | 5 | Blood cholesterol increased |
| 124213372 | 12421337 | 6 | Blood pressure increased |
| 124213372 | 12421337 | 7 | Cerebrovascular accident |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124213372 | 12421337 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124213372 | 12421337 | Drug dose omission | |
| 124213372 | 12421337 | Hospitalisation | |
| 124213372 | 12421337 | Product use issue |
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 |
|---|---|---|---|---|---|---|
| 124213372 | 12421337 | 1 | 2008 | 0 | ||
| 124213372 | 12421337 | 2 | 2008 | 0 | ||
| 124213372 | 12421337 | 3 | 2008 | 0 | ||
| 124213372 | 12421337 | 4 | 20140430 | 0 | ||
| 124213372 | 12421337 | 5 | 20140430 | 0 | ||
| 124213372 | 12421337 | 6 | 20140430 | 0 | ||
| 124213372 | 12421337 | 7 | 20140430 | 0 |