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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577640 | 6517026 | I | 5577640-X | 20071205 | 20071205 | 20071231 | EXP | US-BAYER-200717292NA | BAYER PHARMACEUTICALS CORPORATION | 52 | YR | F | Y | 66 | KG | 20071231 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577640 | 1009349364 | PS | MAGNEVIST | 1 | INTRAVENOUS | TOTAL DAILY DOSE: 13 ML UNIT DOSE: 13 ML | 71531A | 021037 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5577640 | 1009349364 | NUCLEAR MAGNETIC RESONANCE IMAGING |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5577640 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5577640 | DYSPHAGIA |
| 5577640 | DYSPNOEA |
| 5577640 | EYE IRRITATION |
| 5577640 | EYE SWELLING |
| 5577640 | FEELING HOT |
| 5577640 | URTICARIA |
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 |
|---|---|---|---|---|---|
| 5577640 | 1009349364 | 20071205 | 20071205 |