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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4305204 | 4105690 | I | 4305204-4 | 20031201 | 20040116 | 20040223 | PER | SU-2004-002063 | SANKYO PHARMA INC. | 70 | YR | F | N | 20040217 | MD |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4305204 | 1004655658 | PS | BENICAR | 1 | ORAL | 40 MG QD PO | D | D | 21286 | ||
4305204 | 1004699065 | C | ASPIRIN | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4305204 | 1004655658 | HYPERTENSION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
4305204 | FLATULENCE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4305204 | CR |
4305204 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4305204 | 1004655658 | 20031201 |