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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6919448 | 7537112 | I | 6919448-6 | 20100613 | 20100803 | 20100811 | EXP | B0668240A | GLAXOSMITHKLINE | 57 | YR | F | Y | 20100811 | CN | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6919448 | 1014394019 | PS | LAMICTAL | 1 | ORAL | 25MG PER DAY | UNKNOWN | 020241 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6919448 | 1014394019 | BIPOLAR DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6919448 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6919448 | ALANINE AMINOTRANSFERASE INCREASED |
| 6919448 | ASTHENIA |
| 6919448 | C-REACTIVE PROTEIN INCREASED |
| 6919448 | LYMPHOPENIA |
| 6919448 | PRURITUS |
| 6919448 | RASH ERYTHEMATOUS |
| 6919448 | RASH MACULO-PAPULAR |
| 6919448 | RASH MORBILLIFORM |
| 6919448 | RASH SCARLATINIFORM |
| 6919448 | TOXIC SKIN ERUPTION |
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 |
|---|---|---|---|---|---|
| 6919448 | 1014394019 | 20100520 | 20100615 | 27 | DAY |