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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5849745 | 6735315 | I | 5849745-7 | 20080725 | 20080818 | DIR | 57 | YR | M | N | 103.1 | KG | 20080816 | PH | N | Y | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5849745 | 1010323935 | PS | SIMVASTATIN | 1 | ORAL | 80 MG HS PO | Y | D | 1873914 | 20090801 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5849745 | 1010323935 | HYPERLIPIDAEMIA |
Outcome of event
Event ID | OUTC COD |
---|---|
5849745 | HO |
Reactions reported
Event ID | PT |
---|---|
5849745 | ATRIOVENTRICULAR BLOCK FIRST DEGREE |
5849745 | PANCREATITIS ACUTE |
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 |
---|---|---|---|---|---|
5849745 | 1010323935 | 20080702 | 20080725 |