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
6202694 6968765 F 1 6202694-7 20090224 20090507 20090519 EXP 005911 OTSUKA PHARMACEUTICAL 84 YR M N 20090518 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
6202694 1011627523 PS PLETAL 1 ORAL 50 MG, BID ORAL Y D 20863
6202694 1011660211 C SINGULAIR 1
6202694 1011660212 C SPIRIVA 1
6202694 1011660213 C ENALAPRIL MALEATE 1
6202694 1011660214 C ALDACTONE 1
6202694 1011660215 C ALLOPURINOL 1
6202694 1011660217 C LASIX 1
6202694 1011660219 C ASPIRIN 1
6202694 1011660221 C MUCODYNE (CARBOCISTEINE) 2
6202694 1011660222 C MEXITIL 1
6202694 1011660223 C WARFARIN (WARFARIN POTASSIUM) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6202694 1011627523 PAIN IN EXTREMITY

Outcome of event

Event ID OUTC COD
6202694 HO

Reactions reported

Event ID PT
6202694 ANOREXIA
6202694 DEHYDRATION
6202694 HAEMOGLOBIN DECREASED
6202694 HYPOPHAGIA
6202694 PYREXIA
6202694 RENAL DISORDER
6202694 WHITE BLOOD CELL COUNT DECREASED

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

Event ID RPSR COD
6202694 HP
6202694 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6202694 1011627523 20090204 20090225 22 DAY