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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6763468 | 7418030 | F | 1 | 6763468-1 | 20100527 | 20100608 | EXP | TPA2010A03298 | TAKEDA PHARMACEUTICALS NORTH AMERICA. | 53 | YR | M | N | 20100607 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6763468 | 1013838629 | PS | ACTOS | 1 | ORAL | 45 MG, 1 IN 1 D, PER ORAL | D | D | 21073 | ||
6763468 | 1013871579 | SS | LANTUS | 1 | |||||||
6763468 | 1013871581 | C | LIPITOR | 1 | |||||||
6763468 | 1013871582 | C | DIOVAN | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6763468 | 1013838629 | TYPE 2 DIABETES MELLITUS |
6763468 | 1013871579 | TYPE 2 DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
6763468 | OT |
6763468 | RI |
Reactions reported
Event ID | PT |
---|---|
6763468 | CONVULSION |
6763468 | HYPOGLYCAEMIA |
6763468 | NO THERAPEUTIC RESPONSE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6763468 | CR |
6763468 | HP |
Therapies reported
no results found |