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
6082368 6872073 F 6082368-6 20080219 20090115 20090218 EXP FR-AVENTIS-200814573FR SANOFI-AVENTIS 82 YR M Y 20090218

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
6082368 1011144615 PS LASIX 1 ORAL 16273
6082368 1011144616 SS TAVANIC 2
6082368 1011144617 SS MONO TILDIEM 2 ORAL
6082368 1011144618 SS CARDENSIEL 2 ORAL
6082368 1011144619 SS HEMIGOXINE NATIVELLE 2 ORAL
6082368 1011144620 SS NOVONORM 2 ORAL
6082368 1011144621 SS PERMIXON /00833501/ 2 ORAL
6082368 1011144622 SS AVODART 1 ORAL
6082368 1011144623 SS LERCAN 2 ORAL
6082368 1011144624 SS PREVISCAN /00789001/ 2 ORAL
6082368 1011144625 SS AUGMENTIN '125' 1
6082368 1011144626 SS ROCEPHIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6082368 1011144618 DRUG USE FOR UNKNOWN INDICATION
6082368 1011144620 TYPE 2 DIABETES MELLITUS
6082368 1011144621 MICTURITION DISORDER
6082368 1011144622 BENIGN PROSTATIC HYPERPLASIA
6082368 1011144623 ESSENTIAL HYPERTENSION

Outcome of event

Event ID OUTC COD
6082368 HO

Reactions reported

Event ID PT
6082368 ECZEMA

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
6082368 1011144615 20080327
6082368 1011144616 20080201 20080201
6082368 1011144618 20080327
6082368 1011144623 20080327
6082368 1011144625 20080201 20080201
6082368 1011144626 20080201 20080201