Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7914837 | 8245045 | I | 7914837-5 | 20110518 | 20111108 | 20111115 | EXP | MX-SANOFI-AVENTIS-2011SA073420 | SANOFI-AVENTIS | 82 | YR | F | Y | 20111115 | CN | MEXICO |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7914837 | 1018049388 | PS | LANTUS | 1 | SUBCUTANEOUS | NOWN | 021081 | ||||
| 7914837 | 1018049390 | C | ANTIHYPERTENSIVES | 2 | UNKNOWN | ||||||
| 7914837 | 1018049391 | C | ALL OTHER THERAPEUTIC PRODUCTS | 2 | UNKNOWN | ||||||
| 7914837 | 1018049389 | SS | AMARYL | 1 | ORAL | NOWN | 020496 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7914837 | 1018049388 | TYPE 2 DIABETES MELLITUS |
| 7914837 | 1018049389 | TYPE 2 DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7914837 | HO |
| 7914837 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 7914837 | ACUTE PULMONARY OEDEMA |
| 7914837 | ACUTE RESPIRATORY FAILURE |
| 7914837 | LOSS OF CONSCIOUSNESS |
| 7914837 | DYSPNOEA |
| 7914837 | CHEST PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7914837 | 1018049388 | 20030101 | 20110518 | 8 | YR |
| 7914837 | 1018049390 | 19960101 | |||
| 7914837 | 1018049391 | 20110518 | 20110518 | ||
| 7914837 | 1018049389 | 20030101 | 20110518 | 8 | YR |