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
4919806 5922618 F 1 4919806-5 20050601 20060131 20060216 EXP JP_051007866 ELI LILLY AND COMPANY 83 YR F N 38 KG 20060208 OT JAPAN

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
4919806 1006965057 PS EVISTA 1 ORAL 60 MG, DAILY, (1/D), ORAL U D 20815
4919806 1007012311 C EPADEL (ETHYL ICOSAPENTATE) 2
4919806 1007012312 C DIOVAN ^CIBA-GEIGY^ (VALSARTAN) 2
4919806 1007012314 C LEVOTOMIN (LEVOMEPROMAZINE MALEATE) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4919806 1006965057 OSTEOPOROSIS POSTMENOPAUSAL

Outcome of event

Event ID OUTC COD
4919806 HO

Reactions reported

Event ID PT
4919806 ANAEMIA
4919806 SMALL INTESTINAL HAEMORRHAGE

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID RPSR COD
4919806 FGN
4919806 HP
4919806 OTH
4919806 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4919806 1006965057 20050407 20050506