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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6387737 | 7149581 | I | 6387737-2 | 20090714 | 20090930 | EXP | APP200900466 | APP PHARMACEUTICALS | 52 | YR | M | N | 20090929 | LW | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6387737 | 1012374796 | PS | SENSORCAINE | 1 | INTRA-ARTICULAR | CONTINUOUS VIA PUMP, INTRA-ARTICULAR | D | D | 18304 | ||
| 6387737 | 1012432503 | SS | PAIN PUMP | 2 | D | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6387737 | 1012374796 | MUSCULOSKELETAL PAIN |
| 6387737 | 1012432503 | MUSCULOSKELETAL PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6387737 | DS |
Reactions reported
| Event ID | PT |
|---|---|
| 6387737 | JOINT INJURY |
| 6387737 | JOINT RANGE OF MOTION DECREASED |
| 6387737 | MUSCULOSKELETAL DISCOMFORT |
| 6387737 | MUSCULOSKELETAL DISORDER |
| 6387737 | MUSCULOSKELETAL PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6387737 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6387737 | 1012374796 | 20061024 | |||
| 6387737 | 1012432503 | 20061024 |