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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5230994 | 6107443 | F | 5230994-6 | 20060604 | 20070125 | 20070206 | EXP | FR-SANOFI-SYNTHELABO-A02200601993 | SANOFI-SYNTHELABO | 66 | YR | M | Y | 20070206 | OT | FRANCE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5230994 | 1008121295 | SS | CIPROFLOXACIN | 1 | ORAL | UNK | |||||
5230994 | 1008121296 | SS | NIFLURIL | 2 | ORAL | UNK | |||||
5230994 | 1008121297 | PS | XATRAL | 2 | ORAL | UNK | 021287 | ||||
5230994 | 1008121298 | SS | FURADANTIN | 1 | ORAL | UNK |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5230994 | 1008121295 | PROSTATITIS |
5230994 | 1008121296 | PROSTATITIS |
5230994 | 1008121297 | PROSTATITIS |
5230994 | 1008121298 | PROSTATITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
5230994 | HO |
Reactions reported
Event ID | PT |
---|---|
5230994 | BLISTER |
5230994 | EOSINOPHILIA |
5230994 | RASH MACULO-PAPULAR |
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 |
---|---|---|---|---|---|
5230994 | 1008121295 | 20060506 | 20060603 | 29 | DAY |
5230994 | 1008121296 | 20060603 | 20060604 | 2 | DAY |
5230994 | 1008121297 | 20060429 | 20060606 | 39 | DAY |
5230994 | 1008121298 | 20060603 | 20060604 | 2 | DAY |