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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577641 | 6517027 | I | 5577641-1 | 20050101 | 20071226 | 20071231 | PER | US-BAYER-200717095NA | BAYER PHARMACEUTICALS CORPORATION | M | Y | 20071231 | LW | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577641 | 1009349365 | PS | MAGNEVIST | 1 | UNK | 019596 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5577641 | 1009349365 | NUCLEAR MAGNETIC RESONANCE IMAGING ABDOMINAL |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5577641 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5577641 | ANXIETY |
| 5577641 | ASTHENIA |
| 5577641 | COLLAGEN DISORDER |
| 5577641 | NEPHROGENIC SYSTEMIC FIBROSIS |
| 5577641 | PAIN |
| 5577641 | PHYSICAL DISABILITY |
| 5577641 | SKIN DISORDER |
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 |
|---|---|---|---|---|---|
| 5577641 | 1009349365 | 20050801 | 20050801 |