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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6138788 | 6957015 | I | 6138788-4 | 20090323 | 20090331 | EXP | PHHY2009FI10653 | NOVARTIS PHARMACEUTICALS CORP. | M | Y | 20090331 | FINLAND |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6138788 | 1011359250 | PS | STALEVO 100 | 1 | 8 X 150 MG DAILY | 021485 | |||||
| 6138788 | 1011359251 | C | LEVODOPA | 2 | DURING NIGHT | ||||||
| 6138788 | 1011359252 | C | MADOPAR QUICK | 2 | DURING DAY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6138788 | 1011359252 | DRUG EFFECT DECREASED |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6138788 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6138788 | DRUG EFFECT DECREASED |
| 6138788 | DYSPNOEA |
| 6138788 | HYPOVENTILATION |
| 6138788 | PANIC REACTION |
| 6138788 | TREMOR |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |