Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4959785 | 6012928 | F | 4959785-8 | 20051129 | 20060324 | 20060331 | EXP | CO-BOEHRINGER INGELHEIM PHARMACEUTICALS, INC.-2006-BP-03331CL | BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. | M | Y | 20060331 | COLOMBIA |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
4959785 | 1007117973 | PS | SECOTEX CAPSULES | 2 | ORAL | NR | 20579 | ||||
4959785 | 1007117974 | C | METOPROLOL | 2 | ORAL |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4959785 | 1007117973 | BENIGN PROSTATIC HYPERPLASIA |
4959785 | 1007117974 | HYPERTENSION |
Outcome of event
Event ID | OUTC COD |
---|---|
4959785 | LT |
Reactions reported
Event ID | PT |
---|---|
4959785 | HYPOTENSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4959785 | 1007117973 | 20051129 | 20051201 |