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
7403014 7799067 I 7403014-2 20070530 20110321 20110331 EXP 012390 OTSUKA PHARMACEUTICAL CO., LTD. 63 YR F N 20110329 MD UNITED STATES

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
7403014 1016320348 C MELPHALAN HYDROCHLORIDE 1
7403014 1016320370 C FOLIC ACID 1
7403014 1016320377 C VALTREX 1
7403014 1016320351 C TOPROL (METOPROLOL TARTRATE) 2
7403014 1016206949 PS BUSULFEX 1 INTRAVENOUS INTRAVENOUS 020954
7403014 1016320347 SS LASIX 1 20 MG MILLIGRAM(S), BID, D D
7403014 1016320379 C AMBIEN 1
7403014 1016320350 C ANTI-THYMOCYTE GLOBULIN (ANTI-THYMOCYTE GLOBULIN) 2
7403014 1016320380 C PENTAMADINE (PENTAMADINE) 2
7403014 1016320349 C FLUDARABINE (FLUDARABINE) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
7403014 1016206949 STEM CELL TRANSPLANT

Outcome of event

Event ID OUTC COD
7403014 HO
7403014 OT

Reactions reported

Event ID PT
7403014 OEDEMA PERIPHERAL
7403014 BRAIN NATRIURETIC PEPTIDE INCREASED
7403014 DIARRHOEA
7403014 CARDIOMEGALY
7403014 PULMONARY VENO-OCCLUSIVE DISEASE
7403014 DEHYDRATION
7403014 PULMONARY ARTERIAL HYPERTENSION
7403014 PLEURAL EFFUSION

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

Event ID RPSR COD
7403014 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7403014 1016206949 20061001 20061001