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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125922321 | 12592232 | 1 | I | 201604 | 20160719 | 20160726 | 20160726 | PER | US-ELI_LILLY_AND_COMPANY-US201607007647 | ELI LILLY AND CO | 67.25 | YR | M | Y | 0.00000 | 20160726 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125922321 | 12592232 | 1 | PS | CIALIS | TADALAFIL | 1 | Unknown | 20 MG, UNKNOWN | U | 21368 | 20 | MG | TABLET | ||||||
| 125922321 | 12592232 | 2 | SS | CIALIS | TADALAFIL | 1 | Unknown | 5 MG, QD | U | 21368 | 5 | MG | TABLET | QD | |||||
| 125922321 | 12592232 | 3 | SS | TRULICITY | DULAGLUTIDE | 1 | Unknown | UNK, UNKNOWN | U | U | 0 | INJECTION | |||||||
| 125922321 | 12592232 | 4 | C | GLUCOVANCE | GLYBURIDEMETFORMIN HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 125922321 | 12592232 | 5 | C | PENTASA | MESALAMINE | 1 | 500 MG, QID | 0 | 500 | MG | QID | ||||||||
| 125922321 | 12592232 | 6 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | 0 | ||||||||||||
| 125922321 | 12592232 | 7 | C | BENTYL | DICYCLOMINE HYDROCHLORIDE | 1 | 10 MG, UNKNOWN | 0 | 10 | MG | |||||||||
| 125922321 | 12592232 | 8 | C | QUESTRAN | CHOLESTYRAMINE | 1 | 0 | ||||||||||||
| 125922321 | 12592232 | 9 | C | STAXYN | VARDENAFIL HYDROCHLORIDE TRIHYDRATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125922321 | 12592232 | 1 | Benign prostatic hyperplasia |
| 125922321 | 12592232 | 2 | Erectile dysfunction |
| 125922321 | 12592232 | 3 | Product used for unknown indication |
| 125922321 | 12592232 | 8 | Faeces soft |
| 125922321 | 12592232 | 9 | Erectile dysfunction |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125922321 | 12592232 | Crohn's disease | |
| 125922321 | 12592232 | Drug ineffective | |
| 125922321 | 12592232 | Medication residue present |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |