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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127817051 | 12781705 | 1 | I | 2003 | 20160915 | 20160926 | 20160926 | EXP | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-60882BP | BOEHRINGER INGELHEIM | 0.00 | M | Y | 0.00000 | 20160926 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127817051 | 12781705 | 1 | PS | FLOMAX | TAMSULOSIN HYDROCHLORIDE | 1 | Unknown | U | 20579 | ||||||||||
127817051 | 12781705 | 2 | SS | AVODART | DUTASTERIDE | 1 | Oral | 0.5 MG | Y | 5ZP9866 | 0 | .5 | MG | CAPSULE | QD | ||||
127817051 | 12781705 | 3 | SS | DUTASTERIDE. | DUTASTERIDE | 1 | Unknown | Y | 0 | ||||||||||
127817051 | 12781705 | 4 | C | COENZYME Q | 2 | Unknown | 0 | ||||||||||||
127817051 | 12781705 | 5 | C | MAGNESIUM | MAGNESIUM | 1 | Unknown | 0 | |||||||||||
127817051 | 12781705 | 6 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Unknown | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127817051 | 12781705 | 1 | Product used for unknown indication |
127817051 | 12781705 | 2 | Benign prostatic hyperplasia |
127817051 | 12781705 | 3 | Benign prostatic hyperplasia |
127817051 | 12781705 | 4 | Product used for unknown indication |
127817051 | 12781705 | 5 | Product used for unknown indication |
127817051 | 12781705 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127817051 | 12781705 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127817051 | 12781705 | Dizziness | |
127817051 | 12781705 | Drug effect incomplete | |
127817051 | 12781705 | Product substitution issue | |
127817051 | 12781705 | Urinary tract obstruction |
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 |
---|---|---|---|---|---|---|
127817051 | 12781705 | 2 | 2003 | 0 |