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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6771429 | 7437883 | I | 6771429-1 | 20100301 | 20100528 | 20100614 | EXP | AUR-APL-2010-01418 | AUROBINDO PHARMA USA | 45 | YR | M | N | 20100611 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6771429 | 1013874152 | PS | CITALOPRAM | 2 | ORAL | 20MG, DAILY, ORAL | D | D | 77031 | ||
| 6771429 | 1013906740 | C | ALLOPURINOL | 1 | |||||||
| 6771429 | 1013906741 | C | FLIXONASE | 2 | 77031 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6771429 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6771429 | DISCOMFORT |
| 6771429 | PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6771429 | FGN |
| 6771429 | HP |
| 6771429 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6771429 | 1013874152 | 20100301 |