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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5074868 | 6102048 | I | 5074868-2 | 20060214 | 20060802 | 20060809 | EXP | PHRM2006FR02234 | NOVARTIS PHARMACEUTICALS CORP. | 23 | YR | F | Y | 20060809 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5074868 | 1007557892 | PS | GYNERGENE-CAFEINE | 2 | ORAL | 9000 | |||||
| 5074868 | 1007557893 | SS | ACTRON /FRA/ | 2 | ORAL | ||||||
| 5074868 | 1007557894 | SS | RIVOTRIL | 2 | ORAL |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5074868 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5074868 | DRUG DEPENDENCE |
| 5074868 | HEADACHE |
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 |
|---|---|---|---|---|---|
| 5074868 | 1007557892 | 20060214 | |||
| 5074868 | 1007557893 | 20060214 | |||
| 5074868 | 1007557894 | 20060214 |