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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5483734 | 6616114 | I | 5483734-X | 20071004 | 20071009 | DIR | M | N | 204 | LBS | 20071005 | OT | N | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5483734 | 1009033692 | PS | PROLEUKIN | 1 | INTRAVENOUS | 55.5 MU IV Q 8 HOURS | D | ||||
5483734 | 1009049324 | SS | AVASTIN | 1 | INTRAVENOUS | 940 MG IV Q 2 WEEKS | |||||
5483734 | 1009049325 | C | CADUET | 1 | |||||||
5483734 | 1009049326 | C | AMBIEN | 1 | |||||||
5483734 | 1009049327 | C | OXYCONTIN | 1 | |||||||
5483734 | 1009049328 | C | LORTAB | 1 | |||||||
5483734 | 1009049329 | C | ATIVAN | 1 | |||||||
5483734 | 1009049331 | C | VICODIN | 1 | |||||||
5483734 | 1009049332 | C | ZOLOFT | 1 | |||||||
5483734 | 1009049333 | C | TIGAN | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5483734 | HO |
Reactions reported
Event ID | PT |
---|---|
5483734 | PANCREATITIS ACUTE |
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 |
---|---|---|---|---|---|
5483734 | 1009033692 | 20070927 | |||
5483734 | 1009049324 | 20070925 |