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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4919806 | 5922618 | F | 1 | 4919806-5 | 20050601 | 20060131 | 20060216 | EXP | JP_051007866 | ELI LILLY AND COMPANY | 83 | YR | F | N | 38 | KG | 20060208 | OT | JAPAN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4919806 | 1006965057 | PS | EVISTA | 1 | ORAL | 60 MG, DAILY, (1/D), ORAL | U | D | 20815 | ||
4919806 | 1007012311 | C | EPADEL (ETHYL ICOSAPENTATE) | 2 | |||||||
4919806 | 1007012312 | C | DIOVAN ^CIBA-GEIGY^ (VALSARTAN) | 2 | |||||||
4919806 | 1007012314 | C | LEVOTOMIN (LEVOMEPROMAZINE MALEATE) | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4919806 | 1006965057 | OSTEOPOROSIS POSTMENOPAUSAL |
Outcome of event
Event ID | OUTC COD |
---|---|
4919806 | HO |
Reactions reported
Event ID | PT |
---|---|
4919806 | ANAEMIA |
4919806 | SMALL INTESTINAL HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4919806 | FGN |
4919806 | HP |
4919806 | OTH |
4919806 | SDY |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4919806 | 1006965057 | 20050407 | 20050506 |