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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577634 | 6517021 | I | 5577634-4 | 20071204 | 20071221 | 20071231 | EXP | PHBS2007IT21376 | NOVARTIS PHARMACEUTICALS CORP. | 34 | YR | M | Y | 20071229 | OT | ITALY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577634 | 1009349347 | PS | FAMVIR | 1 | ORAL | 750/D | 020363 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5577634 | 1009349347 | HERPES ZOSTER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5577634 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5577634 | ANGER |
| 5577634 | DIARRHOEA |
| 5577634 | HALLUCINATION |
| 5577634 | TACHYCARDIA |
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 |
|---|---|---|---|---|---|
| 5577634 | 1009349347 | 20071203 | 20071205 | 4320 | MIN |