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
5584730 6521621 F 1 5584730-4 20070115 20071220 20080103 EXP 2007-01724 MILLENNIUM PHARMACEUTICALS INC. 78 YR F N 53 KG 20071228 MD 20070512 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
5584730 1009373745 PS VELCADE 1 INTRAVENOUS 1.90 MG, 1.70 MG , 1.30 MG, 1.90 MG INTRAVENOUS Y Y 21602
5584730 1009388902 C PREDNISOLONE 1
5584730 1009388903 C HYDROCORTISONE 1
5584730 1009388904 C WARFARIN SODIUM 1
5584730 1009388905 C ACECOL (TEMOCAPRIL HYDROCHLORIDE) 2
5584730 1009388906 C ENDOXAN 2
5584730 1009388907 C RED BLOOD CELLS 1
5584730 1009388908 C DIFLUCAN 1
5584730 1009388909 C SELBEX (TEPRENONE) 2
5584730 1009388910 C NIVADIL (NILVADIPINE) 2
5584730 1009388911 C LANIRAPID (METILDIGOXIN) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5584730 1009373745 MULTIPLE MYELOMA

Outcome of event

Event ID OUTC COD
5584730 DE
5584730 HO

Reactions reported

Event ID PT
5584730 CARDIAC FAILURE
5584730 DIARRHOEA
5584730 MALIGNANT NEOPLASM PROGRESSION
5584730 NAUSEA
5584730 OEDEMA
5584730 PLATELET COUNT DECREASED
5584730 PULMONARY OEDEMA
5584730 PYREXIA
5584730 WHITE BLOOD CELL COUNT DECREASED

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

Event ID RPSR COD
5584730 FGN
5584730 HP
5584730 OTH
5584730 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5584730 1009373745 20070109 20070109
5584730 1009373745 20070112 20070112
5584730 1009373745 20070130 20070202
5584730 1009373745 20070213 20070323