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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125369611 | 12536961 | 1 | I | 20130820 | 20160707 | 20160707 | PER | US-ELI_LILLY_AND_COMPANY-US201308007962 | ELI LILLY AND CO | 0.00 | M | Y | 0.00000 | 20160707 | CN | US | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125369611 | 12536961 | 1 | PS | CIALIS | TADALAFIL | 1 | Oral | 20 MG, PRN | 21368 | 20 | MG | TABLET | |||||||
| 125369611 | 12536961 | 2 | SS | FLOMAX | TAMSULOSIN HYDROCHLORIDE | 1 | 1 DF, UNKNOWN | U | 0 | 1 | DF | ||||||||
| 125369611 | 12536961 | 3 | SS | FLOMAX | TAMSULOSIN HYDROCHLORIDE | 1 | U | 0 | |||||||||||
| 125369611 | 12536961 | 4 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | 1 DF, UNKNOWN | U | 0 | 1 | DF |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125369611 | 12536961 | 1 | Erectile dysfunction |
| 125369611 | 12536961 | 2 | Dysuria |
| 125369611 | 12536961 | 3 | Prostatomegaly |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125369611 | 12536961 | Arthralgia | |
| 125369611 | 12536961 | Myalgia | |
| 125369611 | 12536961 | Nocturia | |
| 125369611 | 12536961 | Therapeutic response decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |