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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4959787 | 6016863 | I | 4959787-1 | 20060324 | 20060331 | EXP | IT-BOEHRINGER INGELHEIM PHARMACEUTICALS, INC.-2006-DE-01572GD | BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. | Y | 20060331 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4959787 | 1007117979 | PS | TAMSULOSIN HCL | 1 | 20579 | ||||||
4959787 | 1007117980 | SS | AESCULUS HIPPOCASTANUM | 2 | |||||||
4959787 | 1007117981 | SS | DICLOFENAC | 2 | |||||||
4959787 | 1007117982 | SS | OMEPRAZOLE | 1 | |||||||
4959787 | 1007117983 | SS | LEVOFLOXACIN | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4959787 | 1007117979 | CALCULUS URETERIC |
4959787 | 1007117980 | CALCULUS URETERIC |
4959787 | 1007117981 | CALCULUS URETERIC |
Outcome of event
Event ID | OUTC COD |
---|---|
4959787 | HO |
Reactions reported
Event ID | PT |
---|---|
4959787 | ABDOMINAL PAIN |
4959787 | DISEASE RECURRENCE |
4959787 | HYPOTENSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |