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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6749086 | 7377282 | I | 6749086-X | 20100312 | 20100601 | EXP | US-BAYER-201016566NA | BAYER HEALTHCARE PHARMACEUTICALS INC. | 80 | YR | F | Y | 20100601 | MD | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6749086 | 1013783509 | PS | ACARBOSE | 1 | ORAL | 020482 | |||||
| 6749086 | 1013783510 | SS | ACTOS | 1 | ORAL | ||||||
| 6749086 | 1013783511 | SS | GLIPIZIDE | 1 | ORAL | TOTAL DAILY DOSE: 10 MG |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6749086 | 1013783509 | DIABETES MELLITUS |
| 6749086 | 1013783510 | DIABETES MELLITUS |
| 6749086 | 1013783511 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6749086 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6749086 | BLOOD GLUCOSE DECREASED |
| 6749086 | GLAUCOMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |