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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6668640 | 7776549 | I | 6668640-7 | 20100217 | 20100319 | 20100401 | EXP | 2010AL001809 | ACTAVIS ELIZABETH LLC | 47 | YR | F | N | 20100331 | OT | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6668640 | 1013449361 | PS | TRAMADOL HYDROCHLORIDE | 1 | ORAL | 100 MG, TID, PO | N | D | 75960 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6668640 | 1013449361 | PROCEDURAL PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6668640 | DS |
Reactions reported
| Event ID | PT |
|---|---|
| 6668640 | DEHYDRATION |
| 6668640 | NAUSEA |
| 6668640 | RETCHING |
| 6668640 | VOMITING |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6668640 | CR |
| 6668640 | FGN |
| 6668640 | HP |
| 6668640 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6668640 | 1013449361 | 20100217 | 20100217 |