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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125748141 | 12574814 | 1 | I | 20150809 | 20150809 | 20160720 | 20160720 | PER | US-ASTELLAS-2015US028478 | ASTELLAS | 75.00 | YR | F | Y | 0.00000 | 20160720 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125748141 | 12574814 | 1 | PS | VESICARE | SOLIFENACIN SUCCINATE | 1 | Unknown | 21518 | 5 | MG | TABLET | QD | |||||||
| 125748141 | 12574814 | 2 | C | KLONOPIN | CLONAZEPAM | 1 | Unknown | UNK UNK, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125748141 | 12574814 | 1 | Product used for unknown indication |
| 125748141 | 12574814 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125748141 | 12574814 | Abdominal discomfort | |
| 125748141 | 12574814 | Anxiety | |
| 125748141 | 12574814 | Chest discomfort | |
| 125748141 | 12574814 | Dyspepsia | |
| 125748141 | 12574814 | Dysuria | |
| 125748141 | 12574814 | Memory impairment | |
| 125748141 | 12574814 | Urinary retention | |
| 125748141 | 12574814 | Urine flow decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |