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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248791 | 8486009 | I | 8248791-6 | 20111211 | 20120324 | 20120331 | EXP | PHEH2012US006728 | NOVARTIS PHARMACEUTICAL CORPORATION | 62 | YR | F | Y | 70.295 | KG | 20120328 | CN | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248791 | 1019282904 | C | CELEXA | 1 | |||||||
| 8248791 | 1019282905 | C | BACLOFEN | 1 | |||||||
| 8248791 | 1019282907 | C | OXYBUTYNIN | 1 | |||||||
| 8248791 | 1019282903 | PS | GILENYA | 1 | ORAL | 0.5 MG, QD | 022527 | ||||
| 8248791 | 1019282906 | C | LEVOTHYROXINE SODIUM | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8248791 | 1019282903 | MULTIPLE SCLEROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8248791 | LT |
| 8248791 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 8248791 | HEADACHE |
| 8248791 | ROAD TRAFFIC ACCIDENT |
| 8248791 | HYPERTENSION |
| 8248791 | LOSS OF CONSCIOUSNESS |
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 |
|---|---|---|---|---|---|
| 8248791 | 1019282903 | 20111115 | 20111211 | 27 | DAY |