Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125494711 | 12549471 | 1 | I | 20160629 | 20160712 | 20160712 | EXP | IT-VALIDUS PHARMACEUTICALS LLC-IT-2016VAL002257 | VALIDUS | SESSA M., ROSSI C., MASCOLO A., GRASSI E., FIORENTINO S., SCAVONE C.,ET AL. SUSPECTED ADVERSE REACTIONS TO CONTRAST MEDIA IN CAMPANIA REGION (ITALY): RESULTS FROM 14 YEARS OF POST MARKETING SURVEILLANCE. EXPERT OPIN. DRUG SAF.. 2015;14(9):1341-1351 | 49.00 | YR | F | Y | 0.00000 | 20160711 | OT | IT | IT |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125494711 | 12549471 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | UNK | U | 16273 | ||||||||||
125494711 | 12549471 | 2 | C | LAMOTRIGINE. | LAMOTRIGINE | 1 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125494711 | 12549471 | 1 | Product used for unknown indication |
125494711 | 12549471 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125494711 | 12549471 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125494711 | 12549471 | Heart rate increased | |
125494711 | 12549471 | Hypotension | |
125494711 | 12549471 | Rash erythematous |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |