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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7585049 | 8017836 | I | 7585049-2 | 20110620 | 20110621 | 20110630 | EXP | NL-ASTRAZENECA-2011SE37755 | AZPRODUW00 | 78 | YR | F | Y | 20110630 | MD | NETHERLANDS |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7585049 | 1016911387 | C | DICLOFENAC SODIUM | 1 | ORAL | ||||||
| 7585049 | 1016911389 | C | DICLOABAK OOGDRUPPELS | 2 | OPHTHALMIC | 1 MG/ML FLACON 10 ML, 1 GGT DROPS THREE TIMES A DAY | |||||
| 7585049 | 1016911388 | C | DEXAMYTREX OOGDRUPPELS FLACON | 2 | OPHTHALMIC | ||||||
| 7585049 | 1016911386 | C | PROPRANOLOL | 1 | ORAL | ||||||
| 7585049 | 1016911385 | PS | OMEPRAZOLE | 1 | ORAL | 019810 | |||||
| 7585049 | 1016911390 | C | VASELINECETOMACROGOLCREME FNA | 2 | CUTANEOUS |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7585049 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7585049 | CIRCULATORY COLLAPSE |
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 |
|---|---|---|---|---|---|
| 7585049 | 1016911387 | 20110520 | 20110615 | 27 | DAY |
| 7585049 | 1016911389 | 20110520 | |||
| 7585049 | 1016911388 | 20110520 |