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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6733438 | 7394053 | I | 6733438-8 | 20100301 | 20100511 | 20100520 | EXP | FR-KINGPHARMUSA00001-K201000576 | KINGPHARMUSA00001 | 80 | YR | M | Y | 20100520 | CN | FRANCE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6733438 | 1013719538 | PS | ALTACE | 1 | ORAL | UNK | 19901 | ||||
6733438 | 1013719539 | SS | ALTACE | 1 | ORAL | UNK | 019901 | ||||
6733438 | 1013719540 | SS | CORDARONE | 1 | ORAL | 200 MG, QD | |||||
6733438 | 1013719541 | SS | PREVISCAN | 2 | ORAL | UNK | |||||
6733438 | 1013719542 | SS | CARDENSIEL | 2 | ORAL | UNK | |||||
6733438 | 1013719543 | SS | ESOMEPRAZOLE | 2 | ORAL | UNK | |||||
6733438 | 1013719544 | SS | ROSUVASTATIN | 1 | ORAL | UNK |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6733438 | HO |
Reactions reported
Event ID | PT |
---|---|
6733438 | ECCHYMOSIS |
6733438 | ERYSIPELAS |
6733438 | ERYTHEMA |
6733438 | FEELING HOT |
6733438 | PAIN IN EXTREMITY |
6733438 | VASCULAR PURPURA |
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 |
---|---|---|---|---|---|
6733438 | 1013719538 | 20100101 | 20100202 | 33 | DAY |
6733438 | 1013719539 | 20100201 | 20100301 | ||
6733438 | 1013719540 | 20091001 | 20100322 | ||
6733438 | 1013719541 | 20091001 | 20100301 | ||
6733438 | 1013719542 | 20091001 | 20100322 | ||
6733438 | 1013719543 | 20090901 | 20100322 | ||
6733438 | 1013719544 | 20100101 | 20100322 |