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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5117572 | 6139095 | F | 5117572-4 | 20060914 | 20060918 | 20060929 | EXP | AU-ROCHE-463632 | ROCHE | 37 | YR | F | Y | 50.4 | KG | 20060929 | MD | AUSTRALIA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5117572 | 1007716896 | PS | PEGASYS | 1 | UNKNOWN | ||||||
| 5117572 | 1007716897 | C | MOCLOBEMIDE | 2 | |||||||
| 5117572 | 1007716898 | C | OROXINE | 2 | |||||||
| 5117572 | 1007716899 | C | PANAFEN | 2 | REPORTED AS PANAFEN PLUS. DOSAGE REGIMEN REPORTED AS ONE TABLET. |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5117572 | 1007716896 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5117572 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5117572 | INJECTION SITE REACTION |
| 5117572 | THROAT TIGHTNESS |
| 5117572 | URTICARIA |
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 |
|---|---|---|---|---|---|
| 5117572 | 1007716896 | 20060914 | 20060914 | 1 | DAY |
| 5117572 | 1007716897 | 20060615 | |||
| 5117572 | 1007716898 | 19940615 | |||
| 5117572 | 1007716899 | 20050615 |