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
6574426 7155078 F 2 6574426-4 20090623 20100108 20100120 EXP THYM-1001213 GENZYME 58 YR M N 67 KG 20100119 MD 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
6574426 1013086681 PS THYMOGLOBULIN 1 INTRAVENOUS 230 MG, QD, INTRAVENOUS U U C8034NB
6574426 1013166113 C CLOSTRIDIUM BUTYRICUM) 2
6574426 1013166114 C FAMOTIDINE 1
6574426 1013166115 C CYCLOSPORINE 1
6574426 1013166117 C MAGNESIUM OXIDE 2
6574426 1013166161 C METENOLONE ACETATE 2
6574426 1013166162 C POLYMYXIN B SULFATE (POLYMYXIN B SULFATE) 2
6574426 1013166164 C METHYLPREDNISOLONE SODIUM SUCCINATE 2
6574426 1013166171 C DEXCHLORPHENIRAMINE MALEATE 1
6574426 1013166172 C PREDNISOLONE 1
6574426 1013166173 C SENNOSIDE A (SENNOSIDE A) 2
6574426 1013166183 C PENTAMIDINE ISETHIONATE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6574426 1013086681 APLASTIC ANAEMIA

Outcome of event

Event ID OUTC COD
6574426 HO
6574426 OT

Reactions reported

Event ID PT
6574426 CHILLS
6574426 ERYTHEMA MULTIFORME
6574426 FEBRILE NEUTROPENIA
6574426 FUNGAL INFECTION
6574426 INSOMNIA
6574426 OEDEMA
6574426 PETECHIAE
6574426 PLATELET COUNT DECREASED
6574426 PRURITUS
6574426 PYREXIA
6574426 RENAL FAILURE
6574426 SERUM SICKNESS
6574426 STAPHYLOCOCCAL SEPSIS
6574426 WEIGHT INCREASED

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

Event ID RPSR COD
6574426 CR
6574426 FGN
6574426 HP
6574426 OTH
6574426 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6574426 1013086681 20090623 20090627