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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5374941 | 6175836 | F | 5374941-5 | 20061101 | 20070619 | 20070629 | EXP | GB-GILEAD-2006-0010698 | 185049848 | F | Y | 20070629 | MD | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5374941 | 1008647748 | PS | TRUVADA | 1 | 021752 | ||||||
5374941 | 1008647749 | C | EFAVIRENZ | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5374941 | OT |
Reactions reported
Event ID | PT |
---|---|
5374941 | FOCAL GLOMERULOSCLEROSIS |
5374941 | GLOMERULONEPHRITIS PROLIFERATIVE |
5374941 | RENAL FAILURE |
5374941 | SYSTEMIC LUPUS ERYTHEMATOSUS |
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 |
---|---|---|---|---|---|
5374941 | 1008647748 | 20050201 | 20061109 | ||
5374941 | 1008647749 | 20050201 |