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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7008914 | 7608841 | I | 7008914-3 | 20100309 | 20100316 | 20100420 | PER | LMI-2010-00179 | LANTHEUS MEDICAL IMAGING | 29 | YR | F | N | 165 | LBS | 20100324 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7008914 | 1014761117 | PS | ABLAVAR | 1 | INTRAVENOUS | (10 ML),INTRAVENOUS BOLUS | Y | D | T827B | 20120701 | 21711 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7008914 | 1014761117 | ARTERIOGRAM CAROTID |
| 7008914 | 1014761117 | VERTIGO |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 7008914 | NAUSEA |
| 7008914 | THROAT TIGHTNESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 7008914 | HP |
| 7008914 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7008914 | 1014761117 | 20100309 | 20100309 |