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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472367 | 6325728 | F | 5472367-7 | 20060401 | 20070925 | 20070930 | EXP | US-SHR-US-2006-005215 | BERLEX | 36 | YR | F | Y | 20070928 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472367 | 1008989687 | PS | BETASERON | 1 | SUBCUTANEOUS | 8 MIU, EVERY 2D | VA3449A | ||||
| 5472367 | 1008989688 | C | VICODIN | 1 | 7.5 MG, UNK | ||||||
| 5472367 | 1008989689 | C | NAPROXEN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5472367 | 1008989687 | RELAPSING-REMITTING MULTIPLE SCLEROSIS |
| 5472367 | 1008989688 | PAIN |
| 5472367 | 1008989689 | PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5472367 | HO |
| 5472367 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5472367 | CHEST DISCOMFORT |
| 5472367 | EXOSTOSIS |
| 5472367 | FALL |
| 5472367 | INTERVERTEBRAL DISC DEGENERATION |
| 5472367 | INTERVERTEBRAL DISC PROTRUSION |
| 5472367 | LOSS OF CONSCIOUSNESS |
| 5472367 | MULTIPLE SCLEROSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5472367 | 1008989687 | 20030508 |