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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5041735 | 6080428 | I | 5041735-X | 20060622 | 20060630 | EXP | 2006080688 | PFIZER INC | N | 20060629 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5041735 | 1007435648 | PS | VIAGRA | 1 | U | U | 20895 | ||||
5041735 | 1007457411 | SS | CIALIS | 1 | U | U |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5041735 | OT |
Reactions reported
Event ID | PT |
---|---|
5041735 | VENTRICULAR EXTRASYSTOLES |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5041735 | CR |
5041735 | HP |
Therapies reported
no results found |