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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6699441 | 7368202 | I | 6699441-1 | 20100414 | 20100419 | 20100427 | EXP | JP-MERCK-1004USA03882 | MERCK HUMAN HEALTH DIVISION | 70 | YR | F | Y | 20100428 | MD | JAPAN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6699441 | 1013580834 | PS | JANUVIA | 1 | ORAL | ||||||
6699441 | 1013580835 | SS | AMARYL | 1 | ORAL | ||||||
6699441 | 1013580836 | SS | ACTOS | 1 | ORAL | ||||||
6699441 | 1013580837 | SS | LASIX | 1 | ORAL | ||||||
6699441 | 1013580838 | C | UNASYN | 1 | INTRAVENOUS | ||||||
6699441 | 1013580839 | C | THEODRIP | 2 | INTRAVENOUS |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6699441 | 1013580834 | DIABETES MELLITUS |
6699441 | 1013580835 | DIABETES MELLITUS |
6699441 | 1013580836 | DIABETES MELLITUS |
6699441 | 1013580837 | OEDEMA |
6699441 | 1013580838 | PNEUMONIA |
6699441 | 1013580839 | PNEUMONIA |
Outcome of event
Event ID | OUTC COD |
---|---|
6699441 | LT |
Reactions reported
Event ID | PT |
---|---|
6699441 | CARDIAC FAILURE |
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 |
---|---|---|---|---|---|
6699441 | 1013580834 | 20100407 | 20100414 | 8 | DAY |
6699441 | 1013580835 | 20010606 | |||
6699441 | 1013580836 | 20010606 | |||
6699441 | 1013580837 | 20061117 |