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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 128000961 | 12800096 | 1 | I | 20160920 | 20160930 | 20160930 | EXP | BR-ELI_LILLY_AND_COMPANY-BR201609007688 | ELI LILLY AND CO | 0.00 | M | Y | 90.00000 | KG | 20160930 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 128000961 | 12800096 | 1 | PS | CIALIS | TADALAFIL | 1 | Unknown | 1 DF, UNKNOWN | U | U | 21368 | 1 | DF | TABLET | |||||
| 128000961 | 12800096 | 2 | SS | CIALIS | TADALAFIL | 1 | UNK | U | U | 21368 | TABLET |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 128000961 | 12800096 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 128000961 | 12800096 | Arthralgia | |
| 128000961 | 12800096 | Flank pain | |
| 128000961 | 12800096 | Gait disturbance | |
| 128000961 | 12800096 | Joint stiffness | |
| 128000961 | 12800096 | Musculoskeletal stiffness | |
| 128000961 | 12800096 | Pain | |
| 128000961 | 12800096 | Spinal pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |