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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6251392 | 6992424 | I | 6251392-2 | 20090407 | 20090626 | 20090630 | EXP | D0061557A | GLAXOSMITHKLINE | 71 | F | Y | 62 | KG | 20090630 | PH | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6251392 | 1011815415 | PS | VALTREX | 1 | ORAL | 500MG VARIABLE DOSE | 020487 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6251392 | 1011815415 | HERPES VIRUS INFECTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6251392 | DS |
Reactions reported
| Event ID | PT |
|---|---|
| 6251392 | AORTIC ARTERIOSCLEROSIS |
| 6251392 | ASCITES |
| 6251392 | DIAPHRAGMATIC DISORDER |
| 6251392 | EFFUSION |
| 6251392 | INDURATION |
| 6251392 | INGUINAL HERNIA |
| 6251392 | LIVER DISORDER |
| 6251392 | PLEURAL EFFUSION |
| 6251392 | SCOLIOSIS |
| 6251392 | SPINAL OSTEOARTHRITIS |
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 |
|---|---|---|---|---|---|
| 6251392 | 1011815415 | 20070601 |