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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4833380 | 5878122 | F | 2 | 4833380-3 | 20051102 | 20051117 | EXP | USA0508106117 | ELI LILLY AND COMPANY | 35 | YR | M | N | 20051110 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4833380 | 1006645555 | PS | CIALIS | 1 | 20 MG | 21368 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4833380 | 1006645555 | ERECTILE DYSFUNCTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4833380 | HO |
| 4833380 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4833380 | BLINDNESS TRANSIENT |
| 4833380 | BLINDNESS UNILATERAL |
| 4833380 | PAPILLOEDEMA |
| 4833380 | THERAPY NON-RESPONDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4833380 | CR |
| 4833380 | HP |
Therapies reported
| no results found |