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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4524409 | 5697497 | I | 4524409-0 | 20040923 | 20040923 | 20041117 | PER | 2004S1002871 | MYLAN PHARMACEUTICALS INC. | 73 | YR | M | N | 20041018 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4524409 | 1005480447 | PS | APOKYN | 1 | SUBCUTANEOUS | 0.2 MG AS TEST DOSE, SUBCUTANEOUS,ONE DOSE | U | U | 21264 | ||
| 4524409 | 1005501996 | C | TRIMETHOBENZAMIDE | 2 | |||||||
| 4524409 | 1005501997 | C | CARBIDOPA AND LEVODOPA | 1 | |||||||
| 4524409 | 1005501998 | C | MULTIVITAMIN | 1 | |||||||
| 4524409 | 1005501999 | C | HERBALS | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4524409 | 1005480447 | MOBILITY DECREASED |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4524409 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4524409 | BLOOD PRESSURE DIASTOLIC INCREASED |
| 4524409 | BLOOD PRESSURE SYSTOLIC DECREASED |
| 4524409 | FLUSHING |
| 4524409 | HYPERHIDROSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4524409 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4524409 | 1005480447 | 20040923 |