The Safety Rates Drug Report

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Drug     Injury     Quarter    

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