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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4280585 | 4081353 | I | 4280585-9 | 20030101 | 20040120 | 20040101 | EXP | 2004195671BY | PFIZER INC. | UNK | N | 20040126 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4280585 | 1004564112 | PS | DOSTINEX | 1 | ORAL | 0.5 MG, BID, ORAL | U | D | 20664 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4280585 | 1004564112 | LACTATION DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4280585 | LT |
Reactions reported
| Event ID | PT |
|---|---|
| 4280585 | UTERINE HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4280585 | FGN |
| 4280585 | HP |
| 4280585 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4280585 | 1004564112 | 20030101 | 20030101 |