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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5080519 | 6111500 | I | 5080519-3 | 20060724 | 20060809 | EXP | 2006AL001981 | ACTAVIS ELIZABETH LLC | M | N | 20060808 | OT | DENMARK |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5080519 | 1007580235 | PS | DOXAZOSIN MESYLATE | 1 | ORAL | 5 MG; QD; PO | U | D | 75574 | ||
5080519 | 1007596249 | C | ALLOPURINOL | 1 | |||||||
5080519 | 1007596250 | C | THALIDOMIDE | 2 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5080519 | DS |
5080519 | HO |
5080519 | LT |
5080519 | OT |
Reactions reported
Event ID | PT |
---|---|
5080519 | STEVENS-JOHNSON SYNDROME |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5080519 | CR |
5080519 | FGN |
5080519 | HP |
5080519 | OTH |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5080519 | 1007580235 | 20060201 |