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
6538062 7178230 F 1 6538062-8 20090916 20091224 20100111 EXP THYM-1001257 GENZYME 24 YR F N 57 KG 20091231 MD 20090916 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
6538062 1012944691 PS THYMOGLOBULIN 1 INTRAVENOUS 60 MG, QD, INTRAVENOUS U U
6538062 1012990209 C FLUDARABINE PHOSPHATE 1
6538062 1012990224 C CYCLOPHOSPHAMIDE 2
6538062 1012990225 C HYDROCORTISONE SODIUM PHOSPHATE 1
6538062 1012990226 C TACROLIMUS 1
6538062 1012990227 C METHOTREXATE 2
6538062 1012990228 C VORICONAZOLE 2
6538062 1012990229 C UNKNOWN DRUG 2
6538062 1012990230 C ACYCLOVIR 1
6538062 1012990231 C MEROPENEM 1
6538062 1012990232 C VANCOMYCIN HYDROCHLORIDE 1
6538062 1012990233 C NEUPOGEN 1
6538062 1012990234 C DORIPENEM HYDRATE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6538062 1012944691 BONE MARROW CONDITIONING REGIMEN
6538062 1012944691 STEM CELL TRANSPLANT

Outcome of event

Event ID OUTC COD
6538062 DE

Reactions reported

Event ID PT
6538062 CEREBRAL HAEMORRHAGE
6538062 STEM CELL TRANSPLANT

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

Event ID RPSR COD
6538062 CR
6538062 FGN
6538062 HP
6538062 OTH
6538062 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6538062 1012944691 20090827 20090830