Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 90600331 | 9060033 | 1 | I | 20121031 | 0 | 20130207 | 20130207 | DIR | 71.00 | YR | M | N | 190.00000 | LBS | 20130127 | Y | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 90600331 | 9060033 | 1 | PS | CIALIS 20 MG | 1 | ORAL | ONE 20MG PILL WHEN NEEDED | Y | 31-OCT-2013 | 0 | 20 | MG | PILLULES | PRN |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 90600331 | 9060033 | 1 | Erectile dysfunction |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 90600331 | 9060033 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 90600331 | 9060033 | Abdominal discomfort | |
| 90600331 | 9060033 | Drug ineffective | |
| 90600331 | 9060033 | Product formulation issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 90600331 | 9060033 | 1 | 20121214 | 0 | ||
| 90600331 | 9060033 | 1 | 20121223 | 0 |