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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577642 | 6517028 | I | 5577642-3 | 20071210 | 20071220 | 20071231 | PER | DE-BAYER-200718497GPV | BAYER PHARMACEUTICALS CORPORATION | 41 | YR | F | Y | 73 | KG | 20071231 | MD | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577642 | 1009349366 | PS | MAGNEVIST | 1 | INTRAVENOUS | AS USED: 20 ML | 72532D | 019596 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5577642 | 1009349366 | MAMMOGRAM |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5577642 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5577642 | HEADACHE |
| 5577642 | NAUSEA |
| 5577642 | SOMNOLENCE |
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 |
|---|---|---|---|---|---|
| 5577642 | 1009349366 | 20071210 | 20071210 |